作者
Luckner Ulysse, Juanita Cubillos, Jean Chmielewski
发表日期
1995/8
期刊
Journal of the American Chemical Society
卷号
117
期号
32
页码范围
8466-8467
出版商
American Chemical Society
简介
The ability to manipulate the specific conformation of peptides and proteins is an essential feature in the development of novel therapeutic agents and biomaterials. 1 To date there are few examples of designed peptides and proteins with the capacity to change conformation as a result of an internal switching mechanism. 2 In thispaper we describe a strategy to reversibly change the conformation of a cyclic peptide (1) by incorporating a photoresponsive amino acid residue within the peptide. 3 The cyclic peptide was designed to include an azobenzene-containing amino acid (Aza) 3 as the conformational switch; it was flanked by four alanine residues for flexibility and four residues with high propensities to exist in a turn conformation (Gly-Gly-Pro-Asn). 4 The peptide was designed such that when Aza contained a trans azo linkage the peptide portion would exist in an extended conformation, and when isomerized to …
引用总数
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学术搜索中的文章
L Ulysse, J Cubillos, J Chmielewski - Journal of the American Chemical Society, 1995