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Journal of the Brazilian Chemical Society

Print version ISSN 0103-5053

J. Braz. Chem. Soc. vol.8 no.1 São Paulo  1997

https://doi.org/10.1590/S0103-50531997000100012 

ARTICLE

 

Comparative time-course study of aminoacyl- and dipeptidyl-resin hydrolysis

 

 

Guita N. JubilutI; Reinaldo MarchettoII; Eduardo M. CilliI; Eliandre OliveiraI; Antonio Mirandaa, Mineko TominagaI; Clóvis R. NakaieeI

IDepartamento de Biofísica, Universidade Federal de São Paulo, Rua 3 de Maio 100, 04044-020 São Paulo - SP, Brazil
IIDepartamento de Bioquímica, Instituto de Química, Universidade Estadual Paulista 14800-060 Araraquara - SP, Brazil

 

 


ABSTRACT

The classic hydrolysis procedure for quantification of resin-bound aminoacyl and peptidyl groups with 12 N HCl: propionic acid was reevaluated by studying the influence of the nature of the resin and the resin-bound group. Their stability during acid hydrolysis was dependent on the C-terminal amino acid, and the order of acid stability was Phe > Val > Gly. Otherwise, the dipeptides Ala-Gly, Ala-Val, and Ala-Phe displayed enhanced rates of hydrolysis of the resin if compared with their parent aminoacyl groups. Amongthe resins assayed, the order of acid stability was: benzhydrylamine-resin>p-methylbenzhydrylamine-resin ≅4-(oxymethyl)-phenylacetamidomethyl-resin > chloromethyl-copolymer of styrene-1%-divinylbenzene. Important for peptide synthesis method, the findings demonstrate that longer hydrolysis times than previously recommended in the literature (1 h at 130 °C and 15 min at 160 °C for peptides attached to the chloromethyl-copolymer of styrene-1%-divinylbenzene) are necessary for the quantitative acid-catalyzed cleavage of some resin-bound groups. The observed broad range of hydrolysis time varied from less than 1 h to about 100 h.

Keywords: peptide hydrolysis, resin, acid hydrolysis, amino acid analysis, acyl-resin hydrolysis, solid phase peptide synthesis


RESUMO

O método clássico de hidrólise para a quantificação de grupamentos aminoacílicos e peptídicos ligados a resinas em HCl 12 N : ácido propiônico foi reavaliada, estudando-se a influência da natureza da resina e do grupamento ligado à mesma. A estabilidade frente à hidrólise ácida foi dependente do amino acido C-terminal e a ordem de estabilidade ácida foi Phe > Val > Gly. Por outro lado, os dipeptídeos Ala-Gly, Ala-Val e Ala-Phe apresentaram maiores velocidades de hidrólise da resina, se comparadas com a dos correspondentes grupos aminoacílicos. Dentre as resinas testadas, a ordem de estabilidade foi: benzidrilamino-resina>p-metilbenzidrilamino-resina ≅4-(oximetil)-fenilacetamidometil-resina > copolímero de estireno clorometilado, contendo 1% de divinilbenzeno. Importante para a metodologia de síntese de peptídeos, os resultados demonstraram que tempos de hidrólise mais longos do que os propostos há anos na literatura (1 h a 130 °C e 15 min a 160 °C para os peptídeos ligados ao copolímero de estireno clorometilado, contendo 1% de divinilbenzeno), são necessários para uma clivagem quantitativa de alguns grupos ligados à resina. A ampla faixa de tempos de hidrólise observada variou de menos de 1 h até cerca de 100 h.


 

 

Introduction

In solid phase peptide synthesis method1-4, the resin-bound amino acid or peptide content is usually determined through acid hydrolysis of the composite resin, followed by amino acid analysis. However, since the inception of the propionic acid-12 N HCl solution (1:1, v/v) as the standard hydrolysis protocol5-7 , no additional systematic studies have been carried out on the applicability of this procedure to other resins introduced later in the peptide synthesis technique. Moreover, the exact role of other factors in this cleavage reaction, such as the nature and the loading of the aminoacyl or peptidyl groups bound to the resin matrix, has not yet been thorougly investigated.

The goal of the present report is to investigate the influence of these factors and to propose an appropriate hydrolysis procedure for each class of resin-bound group. Among the resins studied, this paper will focus on those employed in the Boc-α amino group protecting the synthesis strategy1,2, i.e., the classic chloromethyl-copolymer of styrene 1% divinylbenzene (CMSD) and the 4-(oxymethyl)-phenylacetamidomethyl-resin (PAMR)8 employed for the synthesis of C-terminal free α-carboxyl peptides, and the benzhydrylamine-resin (BHAR)9 and the p-methylbenzhydrylamine-resin (MBHAR)10 used alternatively for assembling α-carboxamide sequences. To avoid the risk of acid degradation which could hamper the present quantitative time-course hydrolysis study, the acid-stable amino acids Gly, Val and Phe were chosen as the resin-bound residues. The corresponding resin-bound alanyl sequences (Ala-Gly, Ala-Val, and Ala-Phe) were selected not only as models of peptide resins, but also to evaluate the influence of the α-amino group acylation of the C-terminal residue on their rate of acid cleavage from the resin.

 

Materials and Methods

The tert-butyloxycarbonyl (Boc)-amino acids (Gly, Val, Phe, and Ala) were purchased from Bachem, California. The aminoacyl-resins were acquired from the following companies: MBHAR, Sigma; PAMR, Bachem California, and CMSD, Bachem California and Calbiochem-Novabiochem. BHAR was either synthesized in the laboratory or purchased from Watanabe or Bachem California. Unless otherwise stated, the amino acid loading of resins ranged from about 0.3 to 0.6 mmol/g. Solvents and reagents were of analytical grade and purchased from Aldrich or Fluka.

Amino-acyl- or peptidyl-resins were manually synthesized using the solid phase method1,2, and the ninhydrin assay11 was used to check the effectiveness of the coupling reactions. The Boc-NNα-protecting group was removed by trifluoroacetic acid treatment (30% v/v, in dichloromethane for 30 min) prior to the acid cleavage study. Hydrolyses of resins were done with propionic acid:12 N HCl (1:1, v/v at 130 °C or 160 °C) in Pyrex tubes with plastic teflon-coated screw caps (13 cm x 1 cm), and amino acid analyses were performed in a Beckman 6300 amino acid analyzer system.

 

Results and Discussion

Hydrolysis of aminoacyl-resins

Figure 1 displays the time course of the hydrolysis of the four aminoacyl-resins at 130 °C. As expected, regardless of the resin, the small polar Gly residue was much more labile than Val or Phe, in accordance with the well-known higher acid stability of resin-bound hydrophobic residues12. As previously discussed13, the higher stability of Phe compared to the Val residue may be due to the electron withdrawing effect of its benzene ring at the resin linkage, resulting in a higher resistance to acidolytic cleavage.

 

 

The nature of the polymeric support also affected the rate of hydrolysis, irrespective of the resin-bound amino acid. The decreasing order of resin-bound acid stability was: BHAR > MBHAR = PAMR > CMSD (Fig. l). To the best of our knowledge, there are no previous reports on such a comparative study of the hydrolysis of these resins which are widely employed for peptide synthesis. The lower acid stability of CMSD as compared to PAMR, and of MBHAR as compared to BHAR, has already been demonstrated based upon trifluoroacetic14 and hydrogen fluoride10 treatments, respectively. The findings confirmed the very high acid stability of BHAR9,10,15, and also revealed rather similar acid stability properties of the PAMR and MBHAR polymers.

The results suggest that the reaction times recommended in the literature for the hydrolysis procedure, i.e., 2 h with the CMSD resin5-7 or 18 h with the MBHAR/ BHAR resins10 at 130 °C, are not adequate to achieve quantitative removal of resin-linked amino acids. The time required for the complete cleavage of resin-bound amino acids varied from a minimum of approximately 15 h with the most labile Gly-CMSD to a maximum of 100 h with the very stable Phe-BHAR.

As detailed in the Material and Methods section, the aminoacyl- or peptidyl-containing resins used in the present report were also different regarding their loading degree or their commercial source. To determine whether the degree of resin loading affected the hydrolysis results, the hydrolysis data of three Phe-BHAR batches containing 0.44, 0.91, and 1.54 mmol/g of Phe were compared. The two latter samples were obtained from highly amino group-loaded BHAR batches synthesized according to a forceful synthetic protocol16. No significant differences in the acid stability properties of the three resins were detected (data not shown). A possible influence of the source of resins on their hydrolysis behavior was also ruled out, since the two commercial Phe-BHAR batches (purchased from Bachem California and Watanabe) showed similar hydrolysis kinetics when compared to the above-described samples of laboratory-synthesized BHAR. Also, no difference was observed between the Val-CMSD batches from different companies (Bachem California and Calbiochem-Novabiochem, data not shown).

Alternative procedures using temperatures higher than 130 °C have been previously introduced7 to accelerate the hydrolysis reaction. Table 1 presents the time-course data of the hydrolysis of Gly-, Val-, and Phe-resins obtained at 160 °C. As expected, hydrolyses faster than those at 130 °C were observed, but the reaction time necessary to quantitatively cleave the aminoacyl groups ranged from about 4 h (Gly-CMSD) to about 30 h (Phe-BHAR), longer than that recommended in the literature for 160 °C7.

 

 

The hydrolysis of dipeptidyl-resins

The mechanism of the acid hydrolysis of an aminoacyl group bound to the resin matrix irrespective of the nature of the linkage (ester or amide in the case of CMSD/ PAMR or MBHAR / BHAR resins, respectively) is possibly influenced by the free or acylated form of its α-amino group. Thus, to compare with the Gly-, Val-, and Phe-resins, the corresponding dipeptidyl Ala-Gly-, Ala-Val- and Ala-Phe-containing resins were synthesized and studied as to their stability in acid hydrolysis. To avoid the influence of other factors, the same N-terminal acylation group (alanine) was deliberately employed in this comparative study.

Figure 2 shows the results of the hydrolysis experiments with peptidyl-resins at 130 °C. Faster hydrolyses were observed with the peptidyl-resins when compared with the parent aminoacyl-resins (Fig. l). For instance, the hydrolysis time necessary for the total cleavage of the Gly residue from the resin decreased from about 15 h for Gly-CMSD (Fig. 1A) to about 10 h for Ala-Gly-CMSD (Fig. 2A). In the case of Phe-containing resins, the same trend was observed and ranged from about 100 h (Phe-BHAR, Fig. 1D) to 70 h (Ala-Phe-BHAR, Fig. 2D). These findings indicate that the acylation of the α-amino group of the resin-bound amino acid facilitates its hydrolytic removal from the resin.

 

 

Concerning the influence of the type of amino acid or resin, the decreasing order of acid stability for peptidyl-resins paralleled that observed for aminoacyl-resins, being: Ala-Phe > Ala-Val > Ala-Gly and BHAR > MBHAR = PAMR > CMSD.

As expected, under a more severe condition (160 °C), the minimum and maximum hydrolysis times necessary to achieve complete peptidyl cleavage varied from less than 1 h to about 25 h for the labile Ala-Gly-CMSD and the more stable Ala-Phe-BHAR, respectively (Table 2).

 

 

Moreover, the present time-course study also allowed the evaluation of the hydrolysis time necessary for the complete cleavage of the peptide bond between the alanyl residue and Gly, Val, or Phe residues bound to the resin. The results indicate that hydrolysis times of about 2 h (at 130 °C) and about 45 min (at 160 °C) are sufficient for the quantitative cleavage of these peptide bonds. As these hydrolysis times are shorter than those necessary for quantitatively cleaving any resin-bound C-terminal amino acids under the same conditions (see Figs. 1 and 2 and Tables 1 and 2), the Ala/Gly, Ala/Val, and Ala/Phe molar ratios found in amino acid analyses of dipeptidyl-resin hydrolyzates are usually higher than 1.

Table 3 summarizes the results of this study showing the approximate reaction times necessary to quantitatively cleave the resin-bound C-terminal amino acid when alone or in a peptide sequence at 130 °C and at 160 °C. As indicated, this reaction time is strongly dependent on the nature of the resin and its pendant group and also on the hydrolysis temperature. Therefore, it is important to always be aware of the acid-sensitivity of each class of amino acid to hydrolysis conditions for any quantitative amino acid or peptide content- determination in resin. Much longer reaction times than initially reported in the field of peptide chemistry are needed, depending on the resin sample.

 

 

The present report points to the need for further research with alternative protocols which might allow a reduction in resin hydrolysis times. Cleavage experiments with other hydrolytic systems, such as potassium carbonate in the presence of a phase transfer reagent and ultrasound17, triethanolamine, dimethylformamide and aqueous sodium hydroxide18, methanosulfonic acid/propionic acid/water19, and even the application of the microwave approach20, are currently been underway in our laboratory.

 

Acknowledgments

We are indebted to Prof. Antonio C. M. Paiva for valuable comments and suggestions. Financial support from FAPESP and CNPq is gratefully acknowledged.

 

References

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Received: April 26, 1996; August 12, 1996

 

 

FAPESP helped in meeting the publication costs of this article

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