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苯丙氨酸(邻位)-阿片样肽类似物的生物学特性。

Biological properties of Phe(o)-opioid peptide analogues.

作者信息

Lipkowski A W, Misicka A, Hosohata K, Davis P, Yamamura H I, Porreca F, Hruby V J

机构信息

Department of Chemistry, University of Arizona, Tucson 85721, USA.

出版信息

Life Sci. 2001 Jan 12;68(8):969-72. doi: 10.1016/s0024-3205(00)00993-0.

Abstract

Biological properties of new analogues, which represent Phe(o)-propeptides of a variety of opioid peptides, are described. All Phe(o)-opioid analogues expressed both receptor binding affinities and in vitro biological activities at least at the level of the primary opioid peptides. Surprisingly, some of the propeptides expressed slightly higher activity than the primary opioid peptides. Nevertheless, no significant shift in receptor selectivity was observed, which indicate that these Phe(o)-analogues undoubtedly are propeptides. The possible role of membrane proteolytic enzymes associated with opioid receptors in transformation of propeptides is discussed.

摘要

描述了新型类似物的生物学特性,这些类似物代表了多种阿片肽的苯丙氨酸(o)-前体肽。所有苯丙氨酸(o)-阿片类似物均表现出受体结合亲和力和体外生物学活性,至少与初级阿片肽处于同一水平。令人惊讶的是,一些前体肽表现出比初级阿片肽略高的活性。然而,未观察到受体选择性的显著变化,这表明这些苯丙氨酸(o)-类似物无疑是前体肽。讨论了与阿片受体相关的膜蛋白水解酶在原肽转化中的可能作用。

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