酰胺
膜
受体
化学
血管活性肠肽
GTP'
环化酶
腺苷酸激酶
肽
离解常数
组氨酸
结合位点
生物化学
立体化学
氨基酸
神经肽
酶
作者
Gerd Richter,Rüdiger Göke,Burkhard Göke,Rudolf Arnold
出处
期刊:FEBS Letters
[Wiley]
日期:1990-07-02
卷期号:267 (1): 78-80
被引量:43
标识
DOI:10.1016/0014-5793(90)80292-q
摘要
Specific binding of 125I-labelled GLP-1(7-36)amide to rat lung membranes was dependent upon time and temperature and was proportional to membrane protein concentration. Binding was inhibited in a concentration-dependent manner by unlabelled GLP-1(7-36)amide consistent with the presence of a single class of binding sites with a dissociation constant (Kd) of 1.67 +/- 0.29 nmol/l. GLP-1(1-36)amide was 260 times less potent in inhibiting the binding of 125I-labelled GLP-1(7-36)amide to lung membranes (Kd of 448 +/- 93 nmol/l). Vasoactive intestinal polypeptide and peptide-histidine-isoleucine also displaced 125I-labelled GLP-1(7-36)amide from the receptor concentration-dependently; the Kd was 4.31 +/- 0.8 and 7.93 +/- 4.79 nmol/l, respectively. Guanine nucleotides (GTP-gamma-S, GDP-beta-S) decreased the binding of 125I-labelled GLP-1(7-36)amide to rat lung membranes as was found for GLP-1(7-36)amide receptors in RINm5F cells which were also shown to be coupled to the adenylate cyclase system.
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