Home LiteratureArticle Details
PMID: 11273595 Published · ppublish English

Phenylisoserine: a versatile amino acid for the construction of novel beta-peptide structures.

Journal of the American Chemical Society ·Vol. 123 ·No. 1 ·2001-09-06

Motorina I A, Huel C, Quiniou E, Mispelter J, Adjadj E, Grierson D S

Abstract

The N-Boc O-tert-butyldimethysilyl-substituted hexa-beta-peptide methyl ester 18 was constructed from the O-TBS ether of (-)-(2R, 3S)-phenylisoserine. By NMR, it was determined that this homo beta-peptide adopts a highly stable beta-strand-type secondary structure in chloroform solution, which is stabilized by both hydrophobic interactions involving the OTBS methyl groups of residues i and i + 2, and inter-(five-membered)/intra (six-membered)-residue H-bonding interactions. These interactions are systematically repeated along the peptide chain and, thereby, operate in concert to stabilize the observed conformation of 18.

Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
Published
2001-09-06
Indexed
2001-05-31
Updated
2013-11-21
Language
English
Country/Region
United States
NLM ID
7503056
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]