Solid-phase peptide synthesis in highly loaded conditions


Autoria(s): Nakaie, Clovis R.; Oliveira, Eliandre; Vicente, Eduardo F.; Jubilut, Guita N.; Souza, Sinval E. G.; Marchetto, Reinaldo; Cilli, Eduardo Maffud
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/02/2011

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

The use of very highly substituted resins has been avoided for peptide synthesis due to the aggravation of chain-chain interactions within beads. To better evaluate this problem, a combined solvation-peptide synthesis approach was herein developed taking as models, several peptide-resins and with peptide contents values increasing up to near 85%. Influence of peptide sequence and loading to solvation characteristics of these compounds was observed. Moreover, chain-chain distance and chain concentration within the bead were also calculated in different loaded conditions. of note, a severe shrinking of beads occurred during the alpha-amine deprotonation step only when in heavily loaded resins, thus suggesting the need for the modification of the solvent system at this step. Finally, the yields of different syntheses in low and heavily loaded conditions were comparable, thus indicating the feasibility of applying this latter prohibitive chemical synthesis protocol. We thought these results might be basically credited to the possibility, without the need of increasing molar excess of reactants, of carrying out the coupling reaction in higher concentration of reactants - near three to seven folds - favored by the use of smaller amount of resin. Additionally, the alteration in the solvent system at the alpha-amine deprotonation step might be also improving the peptide synthesis when in heavily loaded experimental protocol.

Formato

101-109

Identificador

http://dx.doi.org/10.1016/j.bioorg.2011.01.001

Bioorganic Chemistry. San Diego: Academic Press Inc. Elsevier B.V., v. 39, n. 1-3, p. 101-109, 2011.

0045-2068

http://hdl.handle.net/11449/25270

10.1016/j.bioorg.2011.01.001

WOS:000307423100013

Idioma(s)

eng

Publicador

Academic Press Inc. Elsevier B.V.

Relação

Bioorganic Chemistry

Direitos

closedAccess

Palavras-Chave #Peptide #Peptide synthesis #Peptide-resin solvation #Polymer #Polarity
Tipo

info:eu-repo/semantics/article