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  4. Solid-state NMR at natural isotopic abundance for the determination of conformational polymorphism - the case of designed beta-turn peptides containing di-prolines
 
research article

Solid-state NMR at natural isotopic abundance for the determination of conformational polymorphism - the case of designed beta-turn peptides containing di-prolines

Yarava, Jayasubba Reddy  
•
Sonti, Rajesh
•
Kantharaju, K.
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2017
Chemical Communications (ChemComm)

The proton double quantum-carbon single quantum correlation experiment has been applied to designed peptides in the solid state in natural isotopic abundance. Analogous to nOe studies in solution, through-space double-quantum connectivities have been exploited to obtain the cis-trans conformational polymorphism of diproline residues occurring at beta-turns in the peptides.

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Type
research article
DOI
10.1039/c6cc08676d
Web of Science ID

WOS:000394244000025

Author(s)
Yarava, Jayasubba Reddy  
Sonti, Rajesh
Kantharaju, K.
Raghothama, S.
Ramanathan, K. V.
Date Issued

2017

Publisher

Royal Society of Chemistry

Published in
Chemical Communications (ChemComm)
Volume

53

Issue

7

Start page

1317

End page

1320

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
ISIC  
Available on Infoscience
May 1, 2017
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/136688
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