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新型荧光血管紧张素II探针的研发

Development of a new fluorescent angiotensin II probe.

作者信息

Fatigati V, Peach M J

机构信息

Department of Pharmacology, University of Virginia School of Medicine, Charlottesville 22908.

出版信息

Am J Physiol. 1988 Oct;255(4 Pt 1):C452-8. doi: 10.1152/ajpcell.1988.255.4.C452.

Abstract

Angiotensin II (ANG II) was conjugated to polystyrene Latex fluorescent microspheres (0.5 or 0.05 micron diam) with carbodiimide. Biological activity of the ANG II-conjugated microspheres (ANG II microspheres) was assessed in dispersed hepatocytes. The 0.05 micron ANG II microspheres inhibited glucagon-stimulated adenosine 3',5'-cyclic monophosphate accumulation and stimulated phosphorylase activity in hepatocytes, whereas the 0.5 micron ANG II microspheres only stimulated phosphorylase activity. The biological activity of the ANG II microspheres was caused by the conjugated ANG II and not by "free" ANG II associated with the spheres or by trypsin-like activity of hepatocytes causing release of ANG II from the microspheres. Binding of 0.05 micron ANG II to hepatocytes was readily observed with fluorescence microscopy. Little, if any, binding was observed with microspheres without conjugated ANG II. This fluorescent preparation of ANG II may have great utility in the study of receptor behavior after binding in individual cells.

摘要

通过碳二亚胺将血管紧张素II(ANG II)与聚苯乙烯乳胶荧光微球(直径0.5或0.05微米)偶联。在分散的肝细胞中评估ANG II偶联微球(ANG II微球)的生物活性。0.05微米的ANG II微球抑制肝细胞中胰高血糖素刺激的3',5'-环磷酸腺苷积累,并刺激磷酸化酶活性,而0.5微米的ANG II微球仅刺激磷酸化酶活性。ANG II微球的生物活性是由偶联的ANG II引起的,而不是由与微球相关的“游离”ANG II或肝细胞的类胰蛋白酶活性导致ANG II从微球中释放引起的。用荧光显微镜很容易观察到0.05微米的ANG II与肝细胞的结合。未偶联ANG II的微球几乎没有观察到结合(如果有的话)。这种ANG II的荧光制剂在研究单个细胞中结合后的受体行为方面可能具有很大的用途。

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