Synthesis and characterization of water-soluble macrocyclic peptides stabilizing protein α-turn-Reference-Cited by-同舟云学术

Synthesis and characterization of water-soluble macrocyclic peptides stabilizing protein α-turn

Published:2018 Issue:3 Volume:16 Page:459-471
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Lei¹²³⁴⁵,Coric Pascale⁶²³⁴⁵^ORCID,Zhu Kexin¹²³⁴⁵,Liu Wang-Qing¹²³⁴⁵^ORCID,Vidal Michel¹²³⁴⁵,Bouaziz Serge⁶²³⁴⁵^ORCID,Broussy Sylvain¹²³⁴⁵^ORCID

Affiliation:

1. UMR COMETE 8638 CNRS

2. Université Paris Descartes

3. Faculté de Pharmacie de Paris

4. Sorbonne Paris Cité

5. Paris 75006

6. UMR 8015 CNRS

Abstract

Macrocyclic peptides mimic tight “non-classical” α-turn type II-α_LS found in proteins, as shown by spectroscopic and computational analysis of their equilibrating conformations.

Funder

Centre National de la Recherche Scientifique

Université Paris Descartes

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB02852K

Reference44 articles.

1. Inhibition of α-helix-mediated protein–protein interactions using designed molecules

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4. Comparative α-Helicity of Cyclic Pentapeptides in Water

5. Distinct BimBH3 (BimSAHB) Stapled Peptides for Structural and Cellular Studies

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