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反义同源框:蛋白质中编码生物活性肽的一种新基序。

The antisense homology box: a new motif within proteins that encodes biologically active peptides.

作者信息

Baranyi L, Campbell W, Ohshima K, Fujimoto S, Boros M, Okada H

机构信息

Choju Medical Institute, Noyori Fukushimura Hospital, Toyohashi, Japan.

出版信息

Nat Med. 1995 Sep;1(9):894-901. doi: 10.1038/nm0995-894.

Abstract

Amphiphilic peptides approximately fifteen amino acids in length and their corresponding antisense peptides exist within protein molecules. These regions (termed antisense homology boxes) are separated by approximately fifty amino acids. Because many sense-antisense peptide pairs have been reported to recognize and bind to each other, antisense homology boxes may be involved in folding, chaperoning and oligomer formation of proteins. The antisense homology box-derived peptide CALSVDRYRAVASW, a fragment of human endothelin A receptor, proved to be a specific inhibitor of endothelin peptide (ET-1) in a smooth muscle relaxation assay. The peptide was able to block endotoxin-induced shock in rats as well. Our finding of endothelin receptor inhibitor among antisense homology box-derived peptides indicates that searching proteins for this new motif may be useful in finding biologically active peptides.

摘要

长度约为15个氨基酸的两亲性肽及其相应的反义肽存在于蛋白质分子中。这些区域(称为反义同源框)被大约50个氨基酸隔开。由于已报道许多有义-反义肽对可相互识别并结合,反义同源框可能参与蛋白质的折叠、伴侣作用和寡聚体形成。源自反义同源框的肽CALSVDRYRAVASW,即人内皮素A受体的一个片段,在平滑肌舒张试验中被证明是内皮素肽(ET-1)的特异性抑制剂。该肽还能够阻断大鼠内毒素诱导的休克。我们在源自反义同源框的肽中发现内皮素受体抑制剂表明,在蛋白质中寻找这种新基序可能有助于发现生物活性肽。

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