Literature DB >> 11667883

Correlation between Solvation of Peptide-Resins and Solvent Properties(1).

Eduardo M. Cilli1, Eliandre Oliveira, Reinaldo Marchetto, Clovis R. Nakaie.   

Abstract

The solvation properties of model resin and peptide-resins measured in ca. 30 solvent systems correlated better with the sum of solvent electron acceptor (AN) and electron donor (DN) numbers, in 1:1 proportion, than with other solvent polarity parameters. The high sensitivity of the (AN+DN) term to detect differentiated solvation behaviors of peptide-resins, taken as model of heterogeneous and complex solutes, seems to be in agreement with the previously proposed two-parameter model, where the sum of the Lewis acidity and Lewis basicity characters of solvent are proposed for scaling solvent effect. Besides these physicochemical aspects regarding solute-solvent interactions, important implications of this study for the solid phase peptide synthesis were also observed. Each class of peptide-resin displayed a specific solvation profile that was dependent on the amount and the nature of the resin-bound peptide sequence. Plots of resin swelling versus solvent (AN+DN) values allowed the visualization of a maximum solvation region characteristic for each class of resin. This strategy facilitates the selection of solvent systems for optimal solvation conditions of peptide chains in every step of the entire synthesis cycle. Moreover, only the AN and DN concepts allow the understanding of rules for solvation/shrinking of peptide-resins when in homogeneous or in heterogeneous mixed solvents.

Entities:  

Year:  1996        PMID: 11667883     DOI: 10.1021/jo9611632

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  6 in total

1.  Interpretation of the dissolution of insoluble peptide sequences based on the acid-base properties of the solvent.

Authors:  Luciana Malavolta; Marcelo R S Pinto; Jamile H Cuvero; Clóvis R Nakaie
Journal:  Protein Sci       Date:  2006-06       Impact factor: 6.725

2.  Fluorescence study of conformational properties of melanotropins labeled with aminobenzoic acid.

Authors:  A S Ito; E S Souza; S dos Reis Barbosa; C R Nakaie
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

3.  General and specific solvent effects in optical spectra of ortho-aminobenzoic acid.

Authors:  Marcelo Takara; Amando Siuiti Ito
Journal:  J Fluoresc       Date:  2005-03       Impact factor: 2.217

4.  Solvent effects in optical spectra of ortho-aminobenzoic acid derivatives.

Authors:  Marcelo Takara; Jéssica Karoline Eisenhut; Izaura Yoshico Hirata; Luiz Juliano; Amando Siuiti Ito
Journal:  J Fluoresc       Date:  2009-06-12       Impact factor: 2.217

5.  The spin label amino acid TOAC and its uses in studies of peptides: chemical, physicochemical, spectroscopic, and conformational aspects.

Authors:  Shirley Schreier; José Carlos Bozelli; Nélida Marín; Renata F F Vieira; Clóvis R Nakaie
Journal:  Biophys Rev       Date:  2012-01-21

6.  Application of electron paramagnetic resonance spectroscopy for validation of the novel (AN+DN) solvent polarity scale.

Authors:  Luciana Malavolta; Erick F Poletti; Elias H Silva; Shirley Schreier; Clovis R Nakaie
Journal:  Int J Mol Sci       Date:  2008-07-17       Impact factor: 5.923

  6 in total

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