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固相法合成肽。III. 缓激肽:片段与类似物。

Synthesis of peptides by the solid-phase method. III. Bradykinin: fragments and analogs.

作者信息

Park W K, St-Pierre S A, Barabé J, Regoli D

出版信息

Can J Biochem. 1978 Feb;56(2):92-100. doi: 10.1139/o78-015.

Abstract

The natural sequence of bradykinin (BK) and 55 fragments or analogs of this peptide were perpared via the solid-phase method. The peptides were purified using ion-exchange (O-carboxymethyl(CM) and partition (Sephadex G-25) chromatography. The purity of each peptide was established by paper and thin-layer chromatography, paper electrophoresis, amino acid analysis, and biological assays. The compounds were tested in anesthetized rats (tested in vivo) and in two smooth-muscle preparations (rabbit aorta strip, cat ileum strip) in which BK produces contraction by stimulating specific receptors of different types. Some of the new peptides are interesting in that they either resist pulmonary inactivation, or are more potent than BK itself, or antagonize the myotropic effect of BK in rabbit aorta strips.

摘要

通过固相法制备了缓激肽(BK)及其55种片段或类似物的天然序列。使用离子交换(O-羧甲基(CM))和分配(葡聚糖凝胶G-25)色谱法对肽进行纯化。通过纸层析和薄层层析、纸电泳、氨基酸分析和生物学测定确定每种肽的纯度。在麻醉大鼠(体内试验)和两种平滑肌制剂(兔主动脉条、猫回肠条)中对这些化合物进行测试,在这些制剂中BK通过刺激不同类型的特异性受体产生收缩作用。一些新肽很有趣,因为它们要么抵抗肺部失活,要么比BK本身更有效,要么拮抗BK对兔主动脉条的肌otropic作用。

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