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使用位置扫描合成肽组合文库快速确定阿片受体配体。

The use of positional scanning synthetic peptide combinatorial libraries for the rapid determination of opioid receptor ligands.

作者信息

Dooley C T, Houghten R A

机构信息

Torrey Pines Institute for Molecular Studies, San Diego, CA 92121.

出版信息

Life Sci. 1993;52(18):1509-17. doi: 10.1016/0024-3205(93)90113-h.

Abstract

The application of a new synthetic peptide combinatorial library (SPCL) is described. This library, termed a positional scanning SPCL, contains six positional SPCLs, each of which contains all possible hexameric combinations of 18 of the 20 natural L-amino acids (18(6) = 34,012,224 peptides). Each positional SPCL (O1XXXXX-NH2, XO2XXXX-NH2, XXO3XXX-NH2, XXXO4XX-NH2, XXXXO5X-NH2, and XXXXXO6-NH2) was used to determine the most active amino acid for the six positions of a hexamer. Combinations of these amino acids were used to synthesize 24 individual peptides, which were then tested for activity. The most active peptide found corresponded to a hexameric analogue of methionine-enkephalin. Results obtained in this study are compared to those obtained using the SPCL described earlier (1) (O1O2XXXX-NH2), and the subsequent iterative process.

摘要

本文描述了一种新型合成肽组合文库(SPCL)的应用。该文库称为位置扫描SPCL,包含六个位置SPCL,每个位置SPCL包含20种天然L-氨基酸中18种的所有可能六聚体组合(18(6) = 34,012,224个肽)。每个位置SPCL(O1XXXXX-NH2、XO2XXXX-NH2、XXO3XXX-NH2、XXXO4XX-NH2、XXXXO5X-NH2和XXXXXO6-NH2)用于确定六聚体六个位置上最具活性的氨基酸。这些氨基酸的组合用于合成24个单独的肽,然后对其活性进行测试。发现的最具活性的肽对应于甲硫氨酸脑啡肽的六聚体类似物。将本研究获得的结果与使用先前描述的SPCL(1)(O1O2XXXX-NH2)以及后续迭代过程获得的结果进行比较。

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