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Iterative non-proteinogenic residue incorporation yields α/β-peptides with a helix-loop-helix tertiary structure and high affinity for VEGF

Inhibition of specific protein-protein interactions is attractive for a range of therapeutic applications, but the large and irregularly shaped contact surfaces involved in many such interactions make it challenging to design synthetic antagonists. Here, we describe the development of backbone-modif...

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Bibliografiske detaljer
Udgivet i:Chembiochem
Main Authors: Checco, James W., Gellman, Samuel H.
Format: Artigo
Sprog:Inglês
Udgivet: 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5384266/
https://ncbi.nlm.nih.gov/pubmed/27897370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cbic.201600545
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