Literature DB >> 10679625

Effect of lysine residues on the deamidation reaction of asparagine side chains.

S Capasso1, G Balboni, P Di Cerbo.   

Abstract

The effect of lysine residues on the deamidation reaction of the asparagine side chain has been studied on the peptide and on its lysine-acetylated derivative in a wide range of pH values. The amino acid sequence of these peptides is similar to the local sequence flanking the labile Asn-67 in RNAse A. The experimental data show that Lys influences both the deamidation rate and the relative yield of the two reaction products, i.e., the aspartic acid and beta-aspartic acid containing peptide. These effects are pH dependent and can be rationalized based on the mechanism previously proposed for the deamidation reaction via succinimide derivative. Copyright 2000 John Wiley & Sons, Inc.

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Year:  2000        PMID: 10679625     DOI: 10.1002/(SICI)1097-0282(200002)53:2<213::AID-BIP11>3.0.CO;2-C

Source DB:  PubMed          Journal:  Biopolymers        ISSN: 0006-3525            Impact factor:   2.505


  4 in total

1.  Kinetics and mechanisms of deamidation and covalent amide-linked adduct formation in amorphous lyophiles of a model asparagine-containing Peptide.

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Journal:  Pharm Res       Date:  2011-10-18       Impact factor: 4.200

2.  Quantitative measurement of deamidation in lens betaB2-crystallin and peptides by direct electrospray injection and fragmentation in a Fourier transform mass spectrometer.

Authors:  Noah E Robinson; Kirsten J Lampi; Robert T McIver; Robert H Williams; Wayne C Muster; Gary Kruppa; Arthur B Robinson
Journal:  Mol Vis       Date:  2005-12-28       Impact factor: 2.367

3.  Effect of protein structure on deamidation rate in the Fc fragment of an IgG1 monoclonal antibody.

Authors:  Sandipan Sinha; Lei Zhang; Shaofeng Duan; Todd D Williams; Josef Vlasak; Roxana Ionescu; Elizabeth M Topp
Journal:  Protein Sci       Date:  2009-08       Impact factor: 6.725

4.  The aspartimide problem persists: Fluorenylmethyloxycarbonyl-solid-phase peptide synthesis (Fmoc-SPPS) chain termination due to formation of N-terminal piperazine-2,5-diones.

Authors:  Daniel Samson; Daniel Rentsch; Marco Minuth; Thomas Meier; Günther Loidl
Journal:  J Pept Sci       Date:  2019-07       Impact factor: 1.905

  4 in total

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