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PMID: 1478777 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

In situ neutralization in Boc-chemistry solid phase peptide synthesis. Rapid, high yield assembly of difficult sequences.

International journal of peptide and protein research ·Vol. 40 ·No. 3-4 ·1992-00-00 ·Pages 180-93

Schnölzer M, Alewood P, Jones A, Alewood D, Kent SB

Abstract

Simple, effective protocols have been developed for manual and machine-assisted Boc-chemistry solid phase peptide synthesis on polystyrene resins. These use in situ neutralization [i.e. neutralization simultaneous with coupling], high concentrations (> 0.2 M) of Boc-amino acid-OBt esters plus base for rapid coupling, 100% TFA for rapid Boc group removal, and a single short (30 s) DMF flow wash between deprotection/coupling and between coupling/deprotection. Single 10 min coupling times were used throughout. Overall cycle times were 15 min for manual and 19 min for machine-assisted synthesis (75 residues per day). No racemization was detected in the base-catalyzed coupling step. Several side reactions were studied, and eliminated. These included: pyrrolidonecarboxylic acid formation from Gln in hot TFA-DMF; chain-termination by reaction with excess HBTU; and, chain termination by acetylation (from HOAc in commercial Boc-amino acids). The in situ neutralization protocols gave a significant increase in the efficiency of chain assembly, especially for "difficult" sequences arising from sequence-dependent peptide chain aggregation in standard (neutralization prior to coupling) Boc-chemistry SPPS protocols or in Fmoc-chemistry SPPS. Reported syntheses include HIV-1 protease(1-50,Cys.amide), HIV-1 protease(53-99), and the full length HIV-1 protease(1-99).

MeSH Terms
Acetylation Acyl Carrier Protein/chemical synthesis Chromatography, High Pressure Liquid Formic Acid Esters/chemistry Glutamine/chemistry HIV Protease/chemical synthesis Mass Spectrometry Peptide Fragments/chemical synthesis Peptides/chemical synthesis Polystyrenes Resins, Synthetic Stereoisomerism Time Factors
Chemicals
Acyl Carrier Protein Formic Acid Esters HIV-1 protease (44-48) HIV-1 protease (89-99) Peptide Fragments Peptides Polystyrenes Resins, Synthetic t-butyloxycarbonyl group Glutamine acyl carrier protein (65-74) HIV Protease
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schnölzer M
Scripps Research Institute, La Jolla, CA.
Alewood P
Jones A
Alewood D
Kent S B
Article Info
Journal
International journal of peptide and protein research
Abbr.
Int J Pept Protein Res
ISSN
0367-8377
Published
1992-00-00
Pages
180-93
Language
English
Region
Denmark
NLM ID
0330420
Subset
IM
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