Abstract
Background:
Amphibians inhabit the terrestrial environment, a conquest achieved after several evolutionary steps, which were still insufficient to make them completely independent of the aquatic environment. These processes gave rise to many morphological and physiological changes, making their skin (and cutaneous secretion) rich in bioactive molecules. Among the tree frogs, the secretion is composed mainly of peptides; but alkaloids, proteins and steroids can also be found depending on the species. The most known class of biologically active molecules is the antimicrobial peptides (AMPs) that act against bacteria, fungi and protozoans. Although these molecules are well-studied among the hylids, AMPs ontogeny remains unknown. Therefore, we performed peptidomic and proteomic analyses of Pithecopus nordestinus (formerly Phyllomedusa nordestina) in order to evaluate the peptide content in post-metamorphosed juveniles and adult individuals.
Methods:
Cutaneous secretion of both life stages of individuals was obtained and analyzed by LC-MS/MS after reduction and alkylation of disulfide bonds or reduction, alkylation and hydrolysis by trypsin.
Results:
Differences in the TIC profile of juveniles and adults in both treatments were observed. Moreover, the proteomic data revealed known proteins and peptides, with slight differences in the composition, according to the life stage and the treatment. AMPs were identified, and bradykinin-potentiating peptides were observed in trypsin-treated samples, which suggests a protein source of such peptide (cryptide).
Conclusion:
In general, skin secretion contents were similar between juveniles and adults, varying in quantity, indicating that the different stages of life are reflected in the number of molecules and not on their diversity.
Keywords
Peptides; Peptidomics; Proteins; Proteomics;
Pithecopus nordestinus
; Tree frog
Background
Amphibians were the first vertebrates to inhabit the terrestrial environment. This evolutionary step imposed on them a series of morphological and physiological changes [11. Günther R, Duellman WE, Trueb L. Biology of Amphibians. New York, St. Louis-San Francisco (McGraw Hill Co.). 1986., 22. Pough FH, Janis CM, Heiser JB. Vertebrate Life, Pearson. 2002.]. Most species begin as a free-swimming larva, breathing through gills. After undergoing metamorphosis, these animals start to live in the terrestrial environment, where they breathe through lungs and through the skin. However, these adaptations are insufficient to turn amphibians completely independent of the aquatic environment. For example, their fragile and gelatinous eggs depend, at least, on some humidity to develop [11. Günther R, Duellman WE, Trueb L. Biology of Amphibians. New York, St. Louis-San Francisco (McGraw Hill Co.). 1986., 22. Pough FH, Janis CM, Heiser JB. Vertebrate Life, Pearson. 2002.].
The anuran integument contains glands involved in different physiological process, such as cutaneous respiration, protection and thermoregulation [33. Delfino G, Nosi D, Giachi F. Secretory granule-cytoplasm relationships in serous glands of anurans: ultrastructural evidence and possible functional role. Toxicon. 2001 Aug;39(8):1161-71.-66. Clarke BT. The natural history of amphibian skin secretions, their normal functioning and potential medical applications. Biol Rev Camb Philos Soc. 1997 Aug;72(3):365-79.]. Granular (poison) glands store a secretion involved in chemical defense [44. Toledo RC, Jared C. Cutaneous granular glands and amphibian venoms. Comp Biochem Physiol. Part A Physiol. 1995 May;111(1):1-29., 77. Daly JW, Spande TF, Garraffo HM. Alkaloids from amphibian skin: A tabulation of over eight-hundred compounds. J Nat Prod. 2005 Oct;68(10):1556-75.-1010. Rodríguez C, Rollins-Smith L, Ibáñez R, Durant-Archibold AA, Gutiérrez M. Toxins and pharmacologically active compounds from species of the family Bufonidae (Amphibia, Anura). J Ethnopharmacol. 2017 Feb 23;198:235-54.]. Once released, this secretion may be in contact with the mouth or eye mucosa of a predator and induce instantly symptoms such as ptyalism, hyperemic mucous membranes or nausea, avoiding predation [44. Toledo RC, Jared C. Cutaneous granular glands and amphibian venoms. Comp Biochem Physiol. Part A Physiol. 1995 May;111(1):1-29., 1111. 11. Johnnides S, Green T, Eubig P. Toad Intoxication in the Dog by Rhinella marina: the clinical syndrome and current treatment recommendations. J Am Anim Hosp Assoc. 2016 Jul-Aug;52(4):205-11.].
Granular secretion (or skin secretion) contains high number of biomolecules such as alkaloids, peptides, proteins or steroids and the toxin profile vary greatly among each taxonomic group or even among the species [44. Toledo RC, Jared C. Cutaneous granular glands and amphibian venoms. Comp Biochem Physiol. Part A Physiol. 1995 May;111(1):1-29., 66. Clarke BT. The natural history of amphibian skin secretions, their normal functioning and potential medical applications. Biol Rev Camb Philos Soc. 1997 Aug;72(3):365-79.-99. Conlon JM. Structural diversity and species distribution of host-defense peptides in frog skin secretions. Cell Mol Life Sci. 2011 Jul;68(13):2303-15.]. Due to the high variability regarding the production of toxins, amphibians have been considered as natural apothecaries, capable of producing hundreds of compounds in their skin secretion. [1212. Jared C, Antoniazzi MM. Anfíbios: Biologia e Venenos. In: Cardoso JLC, França FOS, Wen FH, Malaque CMS, Haddad Jr V. Editor’s. Animais peçonhentos no Brasil - Biologia, Clínica e Terapêutica dos Acidentes. Sarvier, São Paulo, p. 317 e 330. 2009.]
Most anuran tadpoles are aquatic and possess different phenotypes. For example, some researches show that when tadpoles are reared in the presence of a predator, they developed behavioral and morphological modifications [1313. Van Buskirk J. A comparative test of the adaptive plasticity hypothesis: relationships between habitat and phenotype in anuran larvae. Am Nat. 2002 Jul;160(1):87-102.-1414. Johnson JB, Saenz D, Adams CK, Hibbitts TJ. Naturally occurring variation in tadpole morphology and performance linked to predator regime. Ecol Evol. 2015;5(15):2991-3002.]. These differences seem also to be reflected in terms of the molecular diversity in their skin secretin. Bókony et al. [1515. Bókony V, Móricz AM, Tóth Z, Gál Z, Kurali A, Mikó Z, et al. Variation in chemical defense among natural populations of common toad, Bufo bufo, tadpoles: the role of environmental factors. J Chem Ecol. 2016 Apr;42(4):329-38.] studied the amount and natural variation of bufadienolides in Bufo bufo tadpoles. The authors observed an increase in toxin production when tadpoles coexist with more competitors. However, they did not find evidences linking a higher predation risk with an increase in chemical defenses in tadpoles.
Some researchers also evaluated the ontogenic toxin variation among bufonids. Hayes et al. [1616. Hayes RA, Crossland MR, Hagman M, Capon RJ, Shine R. Ontogenetic variation in the chemical defenses of cane toads (Bufo marinus): toxin profiles and effects on predators. J Chem Ecol. 2009 Apr;35(4):391-9.] studied the qualitative and quantitative difference of several bufadienolides in Rhinella marina (B. marinus) during different life stages. The results revealed a higher diversity and quantity of bufadienolides in the eggs, which decreased during the tadpole phase and returned to rise after metamorphosis. In another study, Üveges et al. [1717. Üveges B, Fera G, Móricz AM, Krüzselyi D, Bókony V, Hettyey A. Age- and environment-dependent changes in chemical defences of larval and post-metamorphic toads. BMC Evol Biol. 2017 Jun 13;17(1):137-46.] found a rise in the quantity and variety of bufadienolides after hatchling stage in B. bufo. Furthermore, the authors also observed that tadpoles submitted to a limited food availability increased significantly the quantity of bufadienolides when compared to their ad libitum fed conspecifics.
Tree frogs are a widespread group among the anurans. Previously, tree frogs have been grouped into the Hylidae family; however, Duellman et al. [1818. Duellman EW, Marion AB, Hedges SB. Phylogenetics, classification, and biogeography of the treefrogs (Amphibia: Anura: Arboranae). Zootaxa. 2016 Apr 19;4104(1):1-109.] proposed a new phylogeny, classifying tree frogs in tree families: Hylidae, Phyllomedusidae and Pelodryadidae, all belonging to the unranked taxon Arboranae.
Adult tree frog skin secretion is one of the most studied among the anurans, being composed mainly by peptides. Several researches have already characterized biochemically and/or biologically these molecules, attributing to them diverse biological activities, such as antitumoral [1919. Conlon JM, Mechkarska M, Lukic ML, Flatt PR. Potential therapeutic applications of multifunctional host-defense peptides from frog skin as anti-cancer, anti-viral, immunomodulatory, and anti-diabetic agents. Peptides. 2014 Jul;57:67-77.], immunomodulatory and insulinotropic [1919. Conlon JM, Mechkarska M, Lukic ML, Flatt PR. Potential therapeutic applications of multifunctional host-defense peptides from frog skin as anti-cancer, anti-viral, immunomodulatory, and anti-diabetic agents. Peptides. 2014 Jul;57:67-77.-2020. Pantic J, Guilhaudis L, Musale V, Attoub S, Lukic ML, Mechkarska M, et al. Immunomodulatory, insulinotropic, and cytotoxic activities of phylloseptins and plasticin-TR from the Trinidanian leaf frog Phyllomedusa trinitatis. J Pept Sci. 2019 Feb 7;25(4):e3153.], inflammatory [2121. Conceição K, Bruni FM, Pareja-Santos A, Antoniazzi MM, Jared C, Lopes-Ferreira M, et al. Unusual profile of leukocyte recruitment in mice induced by a skin secretion of the tree frog Phyllomedusa hypochondrialis. Toxicon. 2007;49(5):625-33.] or vasoactive [2222. Conceição K, Konno K, de Melo RL, Antoniazzi MM, Jared C, Sciani JM, et al. Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis. Peptides. 2007 Mar;28(3):515-23.]. Besides that, these peptides have a prominent biological effect against microorganisms, such as antimicrobial [99. Conlon JM. Structural diversity and species distribution of host-defense peptides in frog skin secretions. Cell Mol Life Sci. 2011 Jul;68(13):2303-15., 2323. Ladram A, Nicolas P. Antimicrobial peptides from frog skin: biodiversity and therapeutic promises. Front Biosci (Landmark Ed). 2016 Jun 1;21:1341-71.-2424. de Azevedo Calderon L, Silva AAE, Ciancaglini P, Stábeli RG. Antimicrobial peptides from Phyllomedusa frogs: From biomolecular diversity to potential nanotechnologic medical applications. Amino Acids. 2011 Jan;40(1):29-49.], antiparasitic [2525. Pinto EG, Pimenta DC, Antoniazzi MM, Jared C, Tempone AG. Antimicrobial peptides isolated from Phyllomedusa nordestina (Amphibia) alter the permeability of plasma membrane of Leishmania and Trypanosoma cruzi. Exp Parasitol. 2013 Dec;135(4):655-60.], antiviral [1919. Conlon JM, Mechkarska M, Lukic ML, Flatt PR. Potential therapeutic applications of multifunctional host-defense peptides from frog skin as anti-cancer, anti-viral, immunomodulatory, and anti-diabetic agents. Peptides. 2014 Jul;57:67-77., 2626. Mechlia MB, Belaid A, Castel G, Jallet C, Mansfield KL, Fooks AR, et al. Dermaseptins as potential antirabies compounds. Vaccine. 2019 Aug 2;37(33):4694-700.], being known as antimicrobial peptides (AMPs).
Peptidome variation is a known phenomenon. Healthy individuals do present such idiosyncrasy [2727. He K, Wen XY, Li AL, Li T, Wang J, Wang HX, et al. Serum peptidome variations in a healthy population: reference to identify cancer-specific peptides. PLoS One. 2013 May 8;8(5):e63724.] that can occur even daily [2828. Gonzalez N, Iloro I, Duran JA, Elortza F, Suarez T. Evaluation of inter-day and inter-individual variability of tear peptide/protein profiles by MALDI-TOF MS analyses. Mol Vis. 2012;18:1572-82.]. Snakes have had their peptidomic variations assessed and demonstrated to be dependent, for instance, on gender. [2929. Pimenta DC, Prezoto BC, Konno K, Melo RL, Furtado MF, Camargo ACM, et al. Mass spectrometric analysis of the individual variability of Bothrops jararaca venom peptide fraction. Evidence for sex-based variation among the bradykinin-potentiating peptides. Rapid Commun Mass Spectrom. 2007 Mar;21(6):1034-42.] Moreover, snake proteome seems to vary as well based on gender [3030. Zelanis A, Menezes MC, Kitano ES, Liberato T, Tashima AK, Pinto AFM, et al. Proteomic identification of gender molecular markers in Bothrops jararaca venom. J Proteomics. 2016 Apr 29;139:26-37.], post-translation modifications [3131. Andrade-Silva D, Zelanis A, Kitano ES, Junqueira-De-Azevedo ILM, Reis MS, Lopes AS, et al. Proteomic and glycoproteomic profilings reveal that post-translational modifications of toxins contribute to venom phenotype in snakes. J Proteome Res. 2016 Jun 14;15(8):2658-75.] or hunting needs. [3232. Zelanis A, Tashima AK, Rocha MMT, Furtado MF, Camargo ACM, Ho PL, et al. Analysis of the ontogenetic variation in the venom proteome/peptidome of Bothrops jararaca reveals different strategies to deal with prey. J Proteome Res. 2010 May 7;9(5):2278-91.] Moreover, Roelants et al. [3333. Roelants K, Fry BG, Ye L, Stijlemans B, Brys L, Kok P, et al. Origin and functional diversification of an amphibian defense peptide arsenal. PLoS Genet. 2013 Aug;9(8):e1003662.] studied the origin and functional diversification of the amphibian AMPs. However, no research evaluating AMP distribution within the same species, comparing juveniles and adults has ever been performed, to the best of these authors knowledge.
Therefore, in order to evaluate the ontogenetic development of the AMPs and proteins secreted into the amphibian skin, we have performed the peptidomic and proteomic analyses of skin secretion of adult (Figure 1A) and juvenile (Figure 1B) specimens - under different sample preparation approaches - of Pithecopus nordestinus (formerly Phyllomedusa nordestina) and evaluated the peptide and protein content in post-metamorphosed juveniles and adult individuals.
Methods
Specimen collection
Specimens of P. nordestinus (family Phyllomedusidae) were collected in Angicos, Rio Grande do Norte State, Brazil during the rainy season, in February, 2004 (IBAMA 02001.005155/2008-13). They were brought to the Laboratory of Cell Biology of Butantan Institute, both in adult form (n = 15) and still in the form of eggs (3 spawning), that ecloded and developed until the form of complete metamorphosed juveniles (attested by the visual absence of tail). Adults were fed with crickets and cockroaches, and larvae were fed with flocked fish food until metamorphosis and life outside water, when newborn crickets and Drosophyla flies were then offered. All animal procedures were performed in accordance with the standards of the Ethics Committee on Animal Use of Butantan Institute (CEUAIB) (protocol #9532050216).
Secretion attainment
In the laboratory, we collected the cutaneous secretion of adult specimens in the moment that they arrived from the field. Besides, we also collected the skin secretion from the 2-month young forms, when metamorphosis was completed. For the skin secretion collection each anuran was individually immersed in a Becker containing ultrapure water (same amount for each animal) and submitted to gentle mechanical stimulus with the tip of the fingers. Then, the secretions were pooled, according to their respective groups (adult or juvenile), lyophilized and kept in -80°C until we started the study.
Reagents
All the employed reagents were purchased from Sigma Co. (St. Louis, MO, USA), unless otherwise stated.
Sample preparation
Initially, the amount of protein in the skin secretion was determined using the bicinchoninic acid kit. Samples of 50 µg of proteins (two for each adult or juvenile skin secretion) were solubilized in in 100 µL of 8 M urea (diluted in 100 mM Tris-HCl, pH 8.5). Then, it was added 100 mM Tris(2-carboxyethyl)phosphine hydrochloride (TCEP) (dissolved in water, 5 mM final concentration) and incubated for 1h at room temperature; after that, 100 mM iodoacetamide (IAA) (dissolved in water, 10 mM final concentration) was added and the material was incubated for 1h, at room temperature and protected from light.
After the last step, one sample of 50 µg of protein (for each adult or juvenile skin secretion) was lyophilized and analyzed directly in the mass spectrometry, in order to identify natural peptides in the sample (termed non-digested sample). The other sample (50 µg for each adult or juvenile skin secretion) was diluted with 100 mM Tris-HCl pH 8.5 to reach urea concentration to 2 M and digested with 10 µL trypsin (Proteomics Grade, from porcine pancreas, Sigma Aldrich) (10 ng.µL-1 of protein) overnight, at 37 °C. The enzymatic reaction was stopped adding 50% acetonitrile (ACN) / 5% trifluoroacetic acid (TFA) and both materials were lyophilized to be analyzed in the mass spectrometry, in order to find proteins (termed enzymatically digested).
Prior to analyze in the mass spectrometer, both samples (enzymatically digested or non-digested) were desalted and concentrated using a ZipTip® C-18 pipette tips (Millipore, Massachusetts, USA), following the manufacture´s instruction, with final elution with acetonitrile containing 0.1% formic acid. The ZipTip® C-18 step was repeated twice and samples were pooled and dried by Speedvac to remove the solvent.
Mass spectrometry (MS)
For the MS analysis, enzymatically digested or non-digested samples were dissolved in 10 µL of 0.1% formic acid (FA). Two microliter aliquots were inserted in a 15 cm x 50 µm Acclaim PepMap™ C-18 column (Thermo Scientific, Waltham, Massachusetts, USA) coupled to nano-chromatography EASY-nLC 1200 system (Thermo Scientific). The eluted content was automatically inserted in a Q Exactive Plus mass spectrometer (Thermo Scientific). Peptides were eluted in a linear gradient of 4-40% B1 (A1: 0.1% FA; B1: 80% ACN in 0.1% FA), at 300 nL/min during 100 min. Spray voltage was set at 2.5 kV and the mass spectrometer was operated in data dependent mode, in which one full MS scan was acquired in the m/z range of 300-1,500 followed by MS/MS acquisition using higher energy collision dissociation (HCD) of the ten most intense ions from the MS scan. MS and MS/MS spectra were acquired in the Orbitrap analyzer at 70,000 and 17,500 resolution (at 200 m/z), respectively. The maximum injection time and AGC target were set to 25 ms and 3.106 for full MS, and 40 ms and 105 for MS/MS. The minimum signal threshold to trigger fragmentation event, isolation window and normalized collision energy (NCE) were set to, respectively, 2,5.104 cps, 1,4 m/z and 28. A dynamic peak exclusion was applied to avoid the same m/z of being selected for the next 30 seconds.
Data processing
RAW files were directly loaded in the software Peaks Studio V7.0 (BSI, Canada) and the data was processed for de novo peptide sequencing and proteomic identification.[3434. Ma B, Zhang K, Hendrie C, Liang C, Li M, Doherty-Kirby A, et al. PEAKS: Powerful software for peptide de novo sequencing by tandem mass spectrometry. Rapid Commun Mass Spectrom. 2003;17(20):2337-42.] De novo peptide sequencing parameters were: MS and MS/MS error mass 10 ppm and 0.01 Da; methionine oxidation and carbamidomethylation as variable and fixed modification, respectively; when applied, trypsin was selected as the cleavage enzyme; average local confidence (ALC) ≥ 95%.
For proteomic identification the following parameters were adjusted: MS and MS/MS error mass were set to 10 ppm and 0.01 Da; methionine oxidation and carbamidomethylation as variable and fixed modification, respectively; when applied, trypsin was selected as the cleavage enzyme; maximum missed cleavages (3), maximum variable PTMs per peptide (3) and non-specific cleavage (both); the false discovery rate was adjusted to ≤ 0.5%; only proteins with the score ≥ 30 and containing at least 1 unique peptide were considered in this study. All data were analyzed against Phyllomedusinae (taxID: 192732) protein database (1271 entries) that was built by retrieving all UniProt entries associated with this subfamily, compiled on 05/18. Complementary analyses were also performed on the Amphibia (taxID: 8292) and the whole SwissProt databases.
Protein analysis
Proteins identified in the proteomics analyses were grouped according to their gene ontology (GO) annotation, based on the described molecular function. The top ten peptides presenting ALC >95% that were not matched in the proteomic analyses, were individually BLASTed, limited to Phyllomedusinae (taxid: 192732).
Results
Figure 2 presents the total ion chromatogram (TIC) comparison of the reduced/alkylated (non-digested) and the reduced/alkylated/digested (enzymatically digested) samples for juvenile and adult individuals. It is possible to observe that the TIC chromatograms vary between juvenile and adults, in terms of number of peaks and peak group distribution. However, no significant variation observed between the experimental conditions for the same group, i.e., reduced/alkylated and reduced/alkylated/digested for juveniles are similar among themselves.
LC-MS/MS TIC chromatograms for the processed skin secretion of Pithecopus nordestinus, for comparison of the reduced/alkylated and the reduced/alkylated/digested samples of juvenile and adult individuals.
The proteomic data for each experimental condition were processed by Peaks Studio V 7.0, using the default parameters. The number of identified proteins, for each experimental condition was: 214/93 (total/redundancies removed) for reduced/alkylated juvenile; 376/200 (total/redundancies removed) for reduced/alkylated adult; 188/186 (total/redundancies removed) for reduced/alkylated/digested juvenile and 411/151 for reduced/alkylated/digested adult. These data are presented in Additional file 1 Additional file 1. Proteomically identified proteins and peptides for adults and juveniles, in both experimental conditions. .
We extracted the protein identifiers from the results and analyzed them at the UniProt retrieve/ID mapping tool, according to the GO-Molecular Function (MF) identifier. The GO-MF results are present as pie chart, employing the same color-code, in Figure 3. It is noteworthy to mention that two of the three major classes of identified proteins present roughly the same percentage distribution (amphibian defense peptides: ± 35%; antimicrobial: ± 20%) in all analysis. However, the percentage of identified proteins classified as oxidoreductase decreased at half between juvenile/adult reduced + alkylated (± 24%) and juvenile/adult reduced + alkylated + trypsin (± 10%) treatments.
GO molecular function distribution of the identified proteins for Pithecopus nordestinus. (A) Reduced + alkylated from juveniles. (B) Reduced + alkylated from adults. (C) Reduced + alkylated + trypsin from juveniles. (D) Reduced + alkylated + trypsin from adults.
Some proteins classes are present only in adults, for both treatments (with or without digestion): endorphins, hypotensive agents, hydrolases, opioid peptides and hormones were not identified in juveniles, only in adults (Figure 3).
The top ten scored de novo sequenced peptides are presented in Table 1. The top 200 peptides are presented in Additional file 2 Additional file 2. Two hundred top-scored de novo sequenced peptides, together with the full Peaks Studio report. , together with the full Peaks Studio report. One representative Peaks Studio interpreted MS/MS spectrum is presented in Figure 4A, together with the software quality control data, including matching ions (Fig. 4B) and mass errors (Fig. 4C). The depicted spectrum corresponds to a Phylloseptin fragment or analogue, identified for the juvenile individual (reduced/alkylated/digested) (HALNAVSALAK, Table 1).
Top ten most significant (ALC > 95, minimum) de novo sequence peptides for the different experimental conditions and their respective BLAS hit, limited to Phyllomedusinae (taxid:192732)
Representative Peaks Studio interpreted peptide sequencing. (A) MS/MS spectrum presenting the deduced sequence, as well as annotated daughter ions. (B) Ion peak list, with series b (blue) and series y (red) annotated. (C) Graph of error (Da) of each ion identified.
Table 1, as well as Additional file 2 Additional file 2. Two hundred top-scored de novo sequenced peptides, together with the full Peaks Studio report. , present peptides that were exclusively de novo sequenced, regardless they were used or not for proteomic identification. It is possible to observe that for the juveniles, when only reduction and alkylation were performed, eight out of the ten presented peptides are indeed bioactive peptides. When trypsinization was performed on this sample, this figure drops to four peptides, indicating that proteins were also present in the undigested skin secretion. For the adults, these rates were 4:10 and 8:10, respectively. Nevertheless, the same phenomenon could be observed, e.g., the presence of proteins in the cutaneous secretion, as revealed by the enzymatic digestion. The full figures for the de novo sequenced peptides were: 3226 for juveniles reduced + alkylated, 4067 for juveniles (reduced + alkylated) + trypsin, 7533 for adults reduced + alkylated and 10046 for adults (reduced + alkylated) + trypsin. These values were obtained when processing the data using Peaks Studio default filters (data not shown).
We have compared the full datasets obtained after the proteomic processing in order to glimpse on the size of each proteome, regarding the individual’s age. Figure 5 presents the Venn diagrams for these comparisons. It is interesting to observe that, although no replicates were performed (we pooled the secretions), data are consistent: there are circa 100 overlapping identified proteins between juveniles and adults - regardless of sample processing - based on ~150 common peptides. Moreover, the unique protein and peptides were observed in comparison of juveniles and adults, for both methods, indicating that there are some molecules in common in their skin secretion, but on the other hand, several compounds (proteins and peptides) that are present only in adults or juveniles. This information is evident when peptides are being compared, when ~1000 are exclusive of adults and ~350 in juveniles, and ~150 in common.
Venn diagrams displaying the overlapping protein and peptide identification of the contents of Pithecopus nordestinus cutaneous secretion, according to the employed experimental conditions.
Regarding the common proteins identified for juveniles and adults, the top 15 identifications (redundancies removed) are presented in Table 2. It is interesting to note that the reduced + alkylated condition yielded less ‘bioactive’ peptides than the (reduced + alkylated) + trypsin condition, in which all top-15 hits are ‘bioactive’ peptides. The first condition does present identified peptides, but - interestingly - only 5 among the fifteen hits are ‘bioactive’ peptides, the other 10 identifications correspond to physiological proteins. Upon analyses of the proteomic identification data, it is noteworthy to mention that the protein identification was not based on a single peptide, but several peptides covering all protein domains (data not shown).
Top 15 common proteins (redundancies removed) between juvenile and adults, according to the methodological condition presented, sorted by the identification score.
Discussion
The question of the how the Amphibian innate immune response changes along the development has already been assessed. Chen and Robert[3535. Chen G, Robert J. Antiviral immunity in amphibians. Viruses. 2011;3(11):2065-86.] have reviewed this subject and comments on the susceptibility of Xenopus adults and larvae to ranaviruses, being the latter much more susceptible to infection. Authors state that “AMPs may play an important role in inactivating viruses at their portals of entry and controlling infections prior to the onset of adaptive immune responses”. In another review, Romo et al. [3636. Riera Romo M, Pérez-Martínez D, Castillo Ferrer C. Innate immunity in vertebrates: An overview. Immunology. 2016 Jun;148(2):125-39.] present an overview of the innate immunity in vertebrates and analyze several components of this system, including: i) mucous secretion; ii) specialized skin; iii) cell mediate innate immunity; iv) proteins (enzymes, antibodies, cytokines) and v) antimicrobial peptides. Still, these authors comment that the humoral response components are poorly characterized in amphibians and reptiles, “making it difficult to understand the evolution of humoral innate immunity in vertebrates”. Nevertheless, the most important antimicrobial peptide for the immune innate response, the β-defensin, is present in vertebrates, such as fishes, lizards, birds, mammals and amphibians. [3737. Tu J, Li D, Li Q, Zhang L, Zhu Q, Gaur U, et al. Molecular evolutionary analysis of β-defensin peptides in vertebrates. Evol Bioinform Online. 2015;11:105-14.]
On the other hand, it is known that the immune system of tadpoles changes right after the larvae metamorphosis. [3838. Rollins-Smith LA. Metamorphosis and the amphibian immune system. Immunol Rev. 1998 Dec;166:221-30.] Robert and Ohta [3939. Robert J, Ohta Y. Comparative and developmental study of the immune system in Xenopus. Dev Dyn. 2010 Jun 25;238(6):1249-70.] present an schematic overview of Xenopus immune system, and places the juveniles together with tadpoles, in terms of immune response, commenting that this would be a downregulated immune system, when compared to the larvae. Unfortunately, the authors do not evaluate the innate immune response in their work. Rollings et al. [4040. Rollins-Smith LA, Ramsey JP, Pask JD, Reinert LK, Woodhams DC. Amphibian immune defenses against chytridiomycosis: Impacts of changing environments. Integr Comp Biol. 2011 Oct;51(4):552-62.] also corroborate the metamorphosis impact on the cellular immune system.
So, in order to try to fill this information gap, we have biochemically assessed the peptide/protein contents of the cutaneous secretion of P. nordestinus individuals of different ages, specifically: juveniles (2-months old) and adults. Once the Phyllomedusinae has been already called ‘storehouses of bioactive peptides’ by Vittorio Erspamer [4141. Erspamer V, Erspamer GF, Cei JM. Active peptides in the skins of two hundred and thirty American amphibian species. Comp Biochem Physiol Part C. 1986;85(1):125-37.], we chose the omics approach to study the subject, once a considerable large database would be available for datamining (currently, 1271 UniProt entries).
The proposed strategy was pretty straightforward: detect all peptides and proteins present in juvenile and adults and compare the identified molecules. For this, we prepared samples in two ways: i) reduced and alkylated (instead of crude) skin secretion; and ii) reduced, alkylated and trypsin-digested skin secretion.
The TIC chromatograms presented in Figure 2 show that there are already many peptides in the skin secretion, for the trypsin digestion did not significantly increase the number of peaks in the chromatogram (~3k to ~4k and ~7k to ~10k de novo peptides, respectively). Moreover, this figure also shows that the overall number of peptides is larger in adults, corroborating the first hypothesis of this work, i.e., the quantity of peptides changes along the ontogenetic development.
On the other hand, when analyzing Figure 3, it is possible to observe that, in spite of the increase in the number of peptides, the GO molecular function distribution (either digested or not) remains virtually the same, i.e., the diversity of the molecules present in the skin secretion does not change with ontogeny. The digested samples contain, as expected, an increased number of identified proteins, that contribute in the low % distribution.
Ujszegi et al. [4242. Ujszegi J, Móricz ÁM, Krüzselyi D, Hettyey A. Skin toxin production of toads changes during early ontogeny but is not adjusted to the microbiota of the aquatic environment. Evol Ecol. 2017;31:925-36.] performed an ontogenetic analysis of Bufo bufo (Bufonidae family), however, focusing on another class of molecules: steroids. The authors observed a decrease in steroid diversity in adult skin when compared to juvenile. On the other side, adults had a higher total quantity of steroids in the skin. In relation to the individual steroid quantity, each molecule showed an independent variation between the ontogenies.
Although we have performed a shotgun approach, i.e., the skin processed skin secretion solutions were directly analyzed without prior sample processing, we are confident in our results. Figure 4 presents a typical Peaks Studio processed MS/MS spectrum, in which it is possible to observe that: i) the daughter ions are representative of the whole sequence and are present in good relative intensity (panel A); ii) these ions provide enough information for deducing the sequence, particularly due to the presence of complete b and y series (panel B); and iii) the experimental error is very low (below 0,05 Da for daughter ions, panel C).
The quantity and diversity of the commonly identified proteins between juveniles and adults were also approached in this work. Figure 5 presents the Venn diagrams corresponding to these analyses. It is possible to observe that the, regardless of the sample processing, there is a ~1:1:3 proportion among exclusive juveniles:common:exclusive adults proteins based on a ~3:2:15 peptides proportion, for the above mentioned conditions. This means that adults present approximately twice the number of proteins than juveniles and four times the number of peptides; figures that, however, do not double the variety of proteins in adults.
Moreover, since the proportion of identified molecules remained the same in juveniles and adults, one cannot attribute the increase in the number of identified proteins to any specific molecular class, e.g., AMPs alone diversity have augmented. There seems to be an overall increase in the global proteome, in which all new peptides and proteins equally present in the adults’ skin.
Interestingly, there were several top-scored de novo sequenced peptides that are not classical AMPs (Dermaseptin, Phylloseptin, Tryptophyllin and Balteatide - Table 1), so the BIOPEP-UWM [4343. Minkiewicz P, Dziuba J, Iwaniak A, Dziuba M, Darewicz M. BIOPEP database and other programs for processing bioactive peptide sequences. J AOAC Int. 2008 Jul-Aug;91(4):965-80.] database was queried, in search for cryptides. [4444. Pimenta DC, Lebrun I. Cryptides: Buried secrets in proteins. Peptides. 2007 Dec;28(12):2403-10.] Some of these peptides, particularly those derived from the leucine rich repeat containing 8 family, member D, matched this criterion. Their unique C-terminal FPK, a motif often found in ACE-inhibitors [4545. Liu R, Zhu Y, Chen J, Wu H, Shi L, Wang X, et al. Characterization of ACE inhibitory peptides from Mactra veneriformis hydrolysate by Nano-Liquid Chromatography Electrospray Ionization Mass Spectrometry (Nano-LC-ESI-MS) and molecular docking. Mar Drugs. 2014 Jul;12(7):3917-28.], makes it possible that these peptides would present such biological effect. The filamin A interacting protein 1 derived peptide (KNLLKYD) also matches another ACE inhibitor peptide (KRQKYDI), derived from porcine troponin. [4646. Katayama K, Anggraeni HE, Mori T, Ahhmed AM, Kawahara S, Sugiyama M, et al. Porcine skeletal muscle troponin is a good source of peptides with angiotensin-I converting enzyme inhibitory activity and antihypertensive effects in spontaneously hypertensive rats. J Agric Food Chem. 2008 Jan 23;56(2):355-60.] Perhaps, the peptide derived from the opioid receptor XOR1, presenting a C-terminal FWK, could inhibit ACE as well, due to the similarity with the previous presented pattern. Peptide YLDFVR, matching FAT atypical cadherin 1, is similar to DFVAP, an ACE inhibitor from casein. [4747. Schlimme E, Meisel H. Bioactive peptides derived from milk-proteins - structural, physiological and analytical aspects. Nahrung. 1995;39(1):1-20.] Nevertheless, complementary assays are necessary to support this hypothesis.
The fibronectin leucine rich transmembrane protein 3 derived peptide (MLQKNHMV) did not provide any evident match to any known bioactive peptide. However, the C-terminal - MV - is a known dipeptidyl peptidase IV inhibitor (DPP IV inhibitor), as well as the N-terminal; ML. [4848. Lan VTT, Ito K, Ohno M, Motoyama T, Ito S, Kawarasaki Y. Analyzing a dipeptide library to identify human dipeptidyl peptidase IV inhibitor. Food Chem. 2015 May 15;175:66-73.]
Another sequenced peptide of particular interest was WDPALDLKE. This molecule displays features from two hazelnut peptides (DWDPK and AWDPE) that had been characterized as antioxidative peptides. [4949. Liu C, Ren D, Li J, Fang L, Wang J, Liu J, et al. Cytoprotective effect and purification of novel antioxidant peptides from hazelnut (C. heterophylla Fisch) protein hydrolysates. J Funct Foods. 2018 Mar;42:203-15.]
Besides the obvious protective function of the AMPs identified in the skin secretion, we were able to sequence the C-terminal of ‘bioactive peptide 1’ (UniProt P84521), which complete sequence is <EQGEGGPYGGLSPLRFS (<E, pyroglutamic acid). This peptide might be considered a bradykinin potentiating peptide (BPP), due to its sequence features [5050. Sciani JM, Pimenta DC. The modular nature of bradykinin-potentiating peptides isolated from snake venoms. J Venom Anim Toxins incl Trop Dis. 2017 Nov 21;23:45. http://dx.doi.org/10.1186/s40409-017-0134-7.
http://dx.doi.org/10.1186/s40409-017-013...
], but biological studies are still necessary to support this idea. Nevertheless, one actual BPP has already been isolated from Phyllomedusa hypochondrialis [5151. Conceição K, Konno K, de Melo RL, Antoniazzi MM, Jared C, Sciani JM, et al. Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis. Peptides. 2007 Mar;28(3):515-23.], so the current finding is not an isolated event. The short sequence LLPLR, also present in Table 1, matched ‘sauvagine’, which is a 40 amino acid peptide, also presenting a pyroglutamic acid at the N-terminal, which acts on diuresis, cardiovascular system and endocrine glands. [5252. Montecucchi PC, Henschen A. Amino acid composition and sequence analysis of sauvagine, a new active peptide from the skin of Phyllomedusa Savaugei. Int J Pept Protein Res. 1980 Aug;18(2):113-20.] On the other hand, the short sequence LLPLR might be a species-specific variation of the C-terminal of bioactive peptide 1/BPP. However, complementary analyses are required.
Table 2 presents the data derived from the Venn diagrams in which the top-scored 15 proteins commonly identified between juveniles and adults are presented. It is noteworthy to mention that the protein profiles between the trypsin-digested and the undigested samples are profoundly different, namely: the digested sample presents only bioactive peptides (including two kazal-like protein inhibitors that display antibacterial activity but do not inhibit trypsin [5353. Gebhard LG, Carrizo FU, Stern AL, Burgardt NI, Faivovich J, Lavilla E, et al. A Kazal prolyl endopeptidase inhibitor isolated from the skin of Phyllomedusa sauvagii. Eur J Biochem. 2004 Jun;271(11):2117-26.] whereas the undigested sample presents proteins.
The upraise in the number of identified peptides after trypsin digestion may have been caused by the fact that the bioactive peptides would be present in the form of (pre)pro-peptides and trypsin would have processed the peptides, making them detectable to the mass spectrometer, whereas when the sample is undigested, there would be peptides naturally present in the skin secretion, either as cryptides or cellular debris [5454. Rash LD, Morales RAV, Vink S, Alewood PF. De novo sequencing of peptides from the parotid secretion of the cane toad, Bufo marinus (Rhinella marina). Toxicon. 2011 Feb;57(2):208-16.] that, when interpreted by Peaks Studio, derive from those proteins. Additional file 3 Additional file 3. Proteomic identification of NADH-ubiquinone oxidoreductase chain 4 (EC 1.6.5.3) in the skin secretion of Pithecopus nordestinus. (A) Identification of the protein after sample reduction and alkylation. (B) Identification of the protein after sample reduction, alkylation and trypsin digestion. Blue bars: peptides identified by the proteomic approach. Gray bars: de novo sequenced peptides that aligned to the protein, as performed locally by Peaks Studio. presents the peptides that were identified as belonging to NADH-ubiquinone oxidoreductase chain 4 (EC 1.6.5.3), the top scored common protein identified between juveniles and adults. It is possible to observe that protein identification was not based on few peptides, nor was it restricted to a specific domain of protein. The possible role of these peptides as cryptides still need to be evaluated. On the other hand, the presence of peptides derived from the constitutive cellular metabolism in the skin secretion have already been described [5454. Rash LD, Morales RAV, Vink S, Alewood PF. De novo sequencing of peptides from the parotid secretion of the cane toad, Bufo marinus (Rhinella marina). Toxicon. 2011 Feb;57(2):208-16.].
Conclusion
The current study has demonstrated that, for P. nordestinus, the ontogenetic development of the innate immune response (through AMPs) follows the direction towards the increase in the quantity of the secreted molecules, and not towards diversity. Moreover, analyses of the peptidome revealed that there might be new class of bioactive peptides (cryptides) displaying ACE inhibitory activity. These peptides would act in conjunction with the kinins present in the skin, potentiating smooth muscle effects that would serve as an anti-predation mechanism for both juveniles and adults.
References
- 1. Günther R, Duellman WE, Trueb L. Biology of Amphibians. New York, St. Louis-San Francisco (McGraw Hill Co.). 1986.
- 2. Pough FH, Janis CM, Heiser JB. Vertebrate Life, Pearson. 2002.
- 3. Delfino G, Nosi D, Giachi F. Secretory granule-cytoplasm relationships in serous glands of anurans: ultrastructural evidence and possible functional role. Toxicon. 2001 Aug;39(8):1161-71.
- 4. Toledo RC, Jared C. Cutaneous granular glands and amphibian venoms. Comp Biochem Physiol. Part A Physiol. 1995 May;111(1):1-29.
- 5. Larsen EH, Ramlov H. Role of cutaneous surface fluid in frog osmoregulation. Comp Biochem Physiol. A Mol Integr Physiol. 2013 Jul;165(3):365-70.
- 6. Clarke BT. The natural history of amphibian skin secretions, their normal functioning and potential medical applications. Biol Rev Camb Philos Soc. 1997 Aug;72(3):365-79.
- 7. Daly JW, Spande TF, Garraffo HM. Alkaloids from amphibian skin: A tabulation of over eight-hundred compounds. J Nat Prod. 2005 Oct;68(10):1556-75.
- 8. Erspamer V, Falconieri EG, Cei JM. Active peptides in the skins of two hundred and thirty American amphibian species. Comp Biochem Physiol C: Comp Pharmacol. 1986;85(1):125-37.
- 9. Conlon JM. Structural diversity and species distribution of host-defense peptides in frog skin secretions. Cell Mol Life Sci. 2011 Jul;68(13):2303-15.
- 10. Rodríguez C, Rollins-Smith L, Ibáñez R, Durant-Archibold AA, Gutiérrez M. Toxins and pharmacologically active compounds from species of the family Bufonidae (Amphibia, Anura). J Ethnopharmacol. 2017 Feb 23;198:235-54.
- 11. 11. Johnnides S, Green T, Eubig P. Toad Intoxication in the Dog by Rhinella marina: the clinical syndrome and current treatment recommendations. J Am Anim Hosp Assoc. 2016 Jul-Aug;52(4):205-11.
- 12. Jared C, Antoniazzi MM. Anfíbios: Biologia e Venenos. In: Cardoso JLC, França FOS, Wen FH, Malaque CMS, Haddad Jr V. Editor’s. Animais peçonhentos no Brasil - Biologia, Clínica e Terapêutica dos Acidentes. Sarvier, São Paulo, p. 317 e 330. 2009.
- 13. Van Buskirk J. A comparative test of the adaptive plasticity hypothesis: relationships between habitat and phenotype in anuran larvae. Am Nat. 2002 Jul;160(1):87-102.
- 14. Johnson JB, Saenz D, Adams CK, Hibbitts TJ. Naturally occurring variation in tadpole morphology and performance linked to predator regime. Ecol Evol. 2015;5(15):2991-3002.
- 15. Bókony V, Móricz AM, Tóth Z, Gál Z, Kurali A, Mikó Z, et al. Variation in chemical defense among natural populations of common toad, Bufo bufo, tadpoles: the role of environmental factors. J Chem Ecol. 2016 Apr;42(4):329-38.
- 16. Hayes RA, Crossland MR, Hagman M, Capon RJ, Shine R. Ontogenetic variation in the chemical defenses of cane toads (Bufo marinus): toxin profiles and effects on predators. J Chem Ecol. 2009 Apr;35(4):391-9.
- 17. Üveges B, Fera G, Móricz AM, Krüzselyi D, Bókony V, Hettyey A. Age- and environment-dependent changes in chemical defences of larval and post-metamorphic toads. BMC Evol Biol. 2017 Jun 13;17(1):137-46.
- 18. Duellman EW, Marion AB, Hedges SB. Phylogenetics, classification, and biogeography of the treefrogs (Amphibia: Anura: Arboranae). Zootaxa. 2016 Apr 19;4104(1):1-109.
- 19. Conlon JM, Mechkarska M, Lukic ML, Flatt PR. Potential therapeutic applications of multifunctional host-defense peptides from frog skin as anti-cancer, anti-viral, immunomodulatory, and anti-diabetic agents. Peptides. 2014 Jul;57:67-77.
- 20. Pantic J, Guilhaudis L, Musale V, Attoub S, Lukic ML, Mechkarska M, et al. Immunomodulatory, insulinotropic, and cytotoxic activities of phylloseptins and plasticin-TR from the Trinidanian leaf frog Phyllomedusa trinitatis. J Pept Sci. 2019 Feb 7;25(4):e3153.
- 21. Conceição K, Bruni FM, Pareja-Santos A, Antoniazzi MM, Jared C, Lopes-Ferreira M, et al. Unusual profile of leukocyte recruitment in mice induced by a skin secretion of the tree frog Phyllomedusa hypochondrialis. Toxicon. 2007;49(5):625-33.
- 22. Conceição K, Konno K, de Melo RL, Antoniazzi MM, Jared C, Sciani JM, et al. Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis. Peptides. 2007 Mar;28(3):515-23.
- 23. Ladram A, Nicolas P. Antimicrobial peptides from frog skin: biodiversity and therapeutic promises. Front Biosci (Landmark Ed). 2016 Jun 1;21:1341-71.
- 24. de Azevedo Calderon L, Silva AAE, Ciancaglini P, Stábeli RG. Antimicrobial peptides from Phyllomedusa frogs: From biomolecular diversity to potential nanotechnologic medical applications. Amino Acids. 2011 Jan;40(1):29-49.
- 25. Pinto EG, Pimenta DC, Antoniazzi MM, Jared C, Tempone AG. Antimicrobial peptides isolated from Phyllomedusa nordestina (Amphibia) alter the permeability of plasma membrane of Leishmania and Trypanosoma cruzi. Exp Parasitol. 2013 Dec;135(4):655-60.
- 26. Mechlia MB, Belaid A, Castel G, Jallet C, Mansfield KL, Fooks AR, et al. Dermaseptins as potential antirabies compounds. Vaccine. 2019 Aug 2;37(33):4694-700.
- 27. He K, Wen XY, Li AL, Li T, Wang J, Wang HX, et al. Serum peptidome variations in a healthy population: reference to identify cancer-specific peptides. PLoS One. 2013 May 8;8(5):e63724.
- 28. Gonzalez N, Iloro I, Duran JA, Elortza F, Suarez T. Evaluation of inter-day and inter-individual variability of tear peptide/protein profiles by MALDI-TOF MS analyses. Mol Vis. 2012;18:1572-82.
- 29. Pimenta DC, Prezoto BC, Konno K, Melo RL, Furtado MF, Camargo ACM, et al. Mass spectrometric analysis of the individual variability of Bothrops jararaca venom peptide fraction. Evidence for sex-based variation among the bradykinin-potentiating peptides. Rapid Commun Mass Spectrom. 2007 Mar;21(6):1034-42.
- 30. Zelanis A, Menezes MC, Kitano ES, Liberato T, Tashima AK, Pinto AFM, et al. Proteomic identification of gender molecular markers in Bothrops jararaca venom. J Proteomics. 2016 Apr 29;139:26-37.
- 31. Andrade-Silva D, Zelanis A, Kitano ES, Junqueira-De-Azevedo ILM, Reis MS, Lopes AS, et al. Proteomic and glycoproteomic profilings reveal that post-translational modifications of toxins contribute to venom phenotype in snakes. J Proteome Res. 2016 Jun 14;15(8):2658-75.
- 32. Zelanis A, Tashima AK, Rocha MMT, Furtado MF, Camargo ACM, Ho PL, et al. Analysis of the ontogenetic variation in the venom proteome/peptidome of Bothrops jararaca reveals different strategies to deal with prey. J Proteome Res. 2010 May 7;9(5):2278-91.
- 33. Roelants K, Fry BG, Ye L, Stijlemans B, Brys L, Kok P, et al. Origin and functional diversification of an amphibian defense peptide arsenal. PLoS Genet. 2013 Aug;9(8):e1003662.
- 34. Ma B, Zhang K, Hendrie C, Liang C, Li M, Doherty-Kirby A, et al. PEAKS: Powerful software for peptide de novo sequencing by tandem mass spectrometry. Rapid Commun Mass Spectrom. 2003;17(20):2337-42.
- 35. Chen G, Robert J. Antiviral immunity in amphibians. Viruses. 2011;3(11):2065-86.
- 36. Riera Romo M, Pérez-Martínez D, Castillo Ferrer C. Innate immunity in vertebrates: An overview. Immunology. 2016 Jun;148(2):125-39.
- 37. Tu J, Li D, Li Q, Zhang L, Zhu Q, Gaur U, et al. Molecular evolutionary analysis of β-defensin peptides in vertebrates. Evol Bioinform Online. 2015;11:105-14.
- 38. Rollins-Smith LA. Metamorphosis and the amphibian immune system. Immunol Rev. 1998 Dec;166:221-30.
- 39. Robert J, Ohta Y. Comparative and developmental study of the immune system in Xenopus. Dev Dyn. 2010 Jun 25;238(6):1249-70.
- 40. Rollins-Smith LA, Ramsey JP, Pask JD, Reinert LK, Woodhams DC. Amphibian immune defenses against chytridiomycosis: Impacts of changing environments. Integr Comp Biol. 2011 Oct;51(4):552-62.
- 41. Erspamer V, Erspamer GF, Cei JM. Active peptides in the skins of two hundred and thirty American amphibian species. Comp Biochem Physiol Part C. 1986;85(1):125-37.
- 42. Ujszegi J, Móricz ÁM, Krüzselyi D, Hettyey A. Skin toxin production of toads changes during early ontogeny but is not adjusted to the microbiota of the aquatic environment. Evol Ecol. 2017;31:925-36.
- 43. Minkiewicz P, Dziuba J, Iwaniak A, Dziuba M, Darewicz M. BIOPEP database and other programs for processing bioactive peptide sequences. J AOAC Int. 2008 Jul-Aug;91(4):965-80.
- 44. Pimenta DC, Lebrun I. Cryptides: Buried secrets in proteins. Peptides. 2007 Dec;28(12):2403-10.
- 45. Liu R, Zhu Y, Chen J, Wu H, Shi L, Wang X, et al. Characterization of ACE inhibitory peptides from Mactra veneriformis hydrolysate by Nano-Liquid Chromatography Electrospray Ionization Mass Spectrometry (Nano-LC-ESI-MS) and molecular docking. Mar Drugs. 2014 Jul;12(7):3917-28.
- 46. Katayama K, Anggraeni HE, Mori T, Ahhmed AM, Kawahara S, Sugiyama M, et al. Porcine skeletal muscle troponin is a good source of peptides with angiotensin-I converting enzyme inhibitory activity and antihypertensive effects in spontaneously hypertensive rats. J Agric Food Chem. 2008 Jan 23;56(2):355-60.
- 47. Schlimme E, Meisel H. Bioactive peptides derived from milk-proteins - structural, physiological and analytical aspects. Nahrung. 1995;39(1):1-20.
- 48. Lan VTT, Ito K, Ohno M, Motoyama T, Ito S, Kawarasaki Y. Analyzing a dipeptide library to identify human dipeptidyl peptidase IV inhibitor. Food Chem. 2015 May 15;175:66-73.
- 49. Liu C, Ren D, Li J, Fang L, Wang J, Liu J, et al. Cytoprotective effect and purification of novel antioxidant peptides from hazelnut (C. heterophylla Fisch) protein hydrolysates. J Funct Foods. 2018 Mar;42:203-15.
- 50. Sciani JM, Pimenta DC. The modular nature of bradykinin-potentiating peptides isolated from snake venoms. J Venom Anim Toxins incl Trop Dis. 2017 Nov 21;23:45. http://dx.doi.org/10.1186/s40409-017-0134-7
» http://dx.doi.org/10.1186/s40409-017-0134-7 - 51. Conceição K, Konno K, de Melo RL, Antoniazzi MM, Jared C, Sciani JM, et al. Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis. Peptides. 2007 Mar;28(3):515-23.
- 52. Montecucchi PC, Henschen A. Amino acid composition and sequence analysis of sauvagine, a new active peptide from the skin of Phyllomedusa Savaugei. Int J Pept Protein Res. 1980 Aug;18(2):113-20.
- 53. Gebhard LG, Carrizo FU, Stern AL, Burgardt NI, Faivovich J, Lavilla E, et al. A Kazal prolyl endopeptidase inhibitor isolated from the skin of Phyllomedusa sauvagii. Eur J Biochem. 2004 Jun;271(11):2117-26.
- 54. Rash LD, Morales RAV, Vink S, Alewood PF. De novo sequencing of peptides from the parotid secretion of the cane toad, Bufo marinus (Rhinella marina). Toxicon. 2011 Feb;57(2):208-16.
-
Availability of data and materials
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request. -
Funding
The present work was supported by CAPES, FINEP (grant numbers 01.09.0278.04 and 01.12.0450.03), FAPESP (2013/07467-1) and CNPq (grant #406385/2018-1 to DCP). DCP, MMA and CJ is are CNPq fellow researchers (grants 301974/2019-5, 309589/2017-7 and 305266/2019-5, respectively). -
Ethics approval
All animal procedures were performed in accordance with the standards of the Ethics Committee on Animal Use of Butantan Institute (CEUAIB) (protocol #9532050216). -
Consent for publication
Not applicable.
Supplementary material
The following online material is available for this article:
Publication Dates
-
Publication in this collection
02 Apr 2021 -
Date of issue
2021
History
-
Received
06 July 2020 -
Accepted
28 Jan 2021