This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
John A. Robinson, Kerstin Möhle, Michel Favre, Synthesis of New Antibody Hypervariable Loop Mimetics Using a D-Pro-L-Apro Template, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01932
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Synthesis of New Antibody Hypervariable Loop Mimetics Using a D-Pro-L-Apro Template
Michel Favre 1
Kerstin Möhle 1
John A. Robinson 1
1. Institute of Organic Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland
Abstract
The aim of this work is to develop new approaches for the synthesis of protein epitope mimetics. These should be conformationally well defined molecules, that accurately mimick the stuctures and properties of exposed surface regions of peptides and proteins. Here we describe the synthesis and application of a dipeptide template, comprising L-4-aminoproline (Apro) and D-proline (D-Pro), to induce a stable b-hairpin conformation in a loop mimetic based upon the L3 complementarity determining region (CDR) of the anti-haemagglutinin antibody HC19. The loop mimetic comprises the cyclic peptide cyclo-(Leu-Trp-Tyr-Ser-Asn-His-Trp-Val-D-Pro-Apro-), which by NMR is shown to adopt a stable and well defined ß-hairpin conformation in DMSO solution. The observed conformation is essentially identical to that found for the L3 CDR in the crystal structure of the antibody Fab fragment.
Keywords
n/a
Dynamic Behaviour of Cyclic Thiohydroxamic Acid Derivatives Barrier to Rotation about N2O Bonds in 4-Substituted N-Isopropoxythiazole-2(3H)-thiones and N-Isopropoxypyridine-2(1H)-thione