Native Chemical Ligation to Minimize Aspartimide Formation during Chemical Synthesis of Small LDLa Protein
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Title
Native Chemical Ligation to Minimize Aspartimide Formation during Chemical Synthesis of Small LDLa Protein
Authors
Keywords
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Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 22, Issue 3, Pages 1146-1151
Publisher
Wiley
Online
2015-11-27
DOI
10.1002/chem.201503599
References
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- Chemical synthesis and X-ray structure of a heterochiral {D-protein antagonist plus vascular endothelial growth factor} protein complex by racemic crystallography
- (2012) K. Mandal et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Protein Chemical Synthesis by Ligation of Peptide Hydrazides
- (2011) Ge-Min Fang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The Relaxin Peptide Family – Structure, Function and Clinical Applications
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- Aspartimide formation in peptide chemistry: occurrence, prevention strategies and the role of N-hydroxylamines
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- Simultaneous Post-cysteine(S-Acm) Group Removal Quenching of Iodine and Isolation of Peptide by One Step Ether Precipitation
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