Suppr超能文献

通过辐射失活法测定人去唾液酸糖蛋白受体的功能大小

Functional size of the human asialoglycoprotein receptor as determined by radiation inactivation.

作者信息

Schwartz A L, Steer C J, Kempner E S

出版信息

J Biol Chem. 1984 Oct 10;259(19):12025-9.

PMID:6090451
Abstract

The radiation target size of the functional asialoglycoprotein receptor (ASGP-R) in purified plasma membranes was determined for human liver and the human hepatoma cell line, Hep G2, by evaluation of the binding of 125I-asialoorosomucoid. Identical inactivation curves were observed for ASGP-R from normal human liver and post-mortem human liver and exhibited a functional unit of 70,000 daltons. The human hepatoma Hep G2 ASGP-R, in contrast, showed a target size of 140,000 daltons. These results suggest that the functional ligand-binding unit of the human ASGP-R is a multimer of the approximately 34,000-dalton unglycosylated receptor polypeptide (Schwartz, A. L., and Rup, D. (1983) J. Biol. Chem. 258, 11249-11255).

摘要

通过评估¹²⁵I-去唾液酸糖蛋白的结合情况,测定了人肝脏和人肝癌细胞系Hep G2纯化质膜中功能性去唾液酸糖蛋白受体(ASGP-R)的辐射靶标大小。观察到正常人肝脏和尸检人肝脏的ASGP-R具有相同的失活曲线,且表现出一个70,000道尔顿的功能单位。相比之下,人肝癌Hep G2的ASGP-R显示出140,000道尔顿的靶标大小。这些结果表明,人ASGP-R的功能性配体结合单位是约34,000道尔顿未糖基化受体多肽的多聚体(施瓦茨,A.L.,和鲁普,D.(1983年)《生物化学杂志》258, 11249 - 11255)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验