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用编码受体蛋白的cDNA转染后功能性去唾液酸糖蛋白受体的形成。

Formation of functional asialoglycoprotein receptor after transfection with cDNAs encoding the receptor proteins.

作者信息

McPhaul M, Berg P

出版信息

Proc Natl Acad Sci U S A. 1986 Dec;83(23):8863-7. doi: 10.1073/pnas.83.23.8863.

Abstract

The rat asialoglycoprotein receptor (ASGP-R) has been expressed in cultured rat hepatoma cells (HTC cells) after transfection with cloned cDNAs. Fluorescence-activated cell sorting of transfected cells was used to identify the functional cDNA clones and to isolate cells expressing the ASGP-R. Simultaneous or sequential transfections with two cloned cDNAs that encode related but distinctive polypeptide chains were needed to obtain ASGP-R activity; transfection with either cDNA alone failed to produce detectable ASGP-R. The affinity of transduced ASGP-R for asialo orosomucoid is less than that of the native rat ASGP-R, and the number of surface receptors in clones expressing ASGP-R is about one-fifth that found on rat hepatocytes.

摘要

用克隆的互补脱氧核糖核酸(cDNA)转染后,大鼠去唾液酸糖蛋白受体(ASGP-R)已在培养的大鼠肝癌细胞(HTC细胞)中表达。利用转染细胞的荧光激活细胞分选来鉴定功能性cDNA克隆,并分离表达ASGP-R的细胞。为了获得ASGP-R活性,需要同时或顺序用两个编码相关但不同多肽链的克隆cDNA进行转染;单独用任何一个cDNA转染均未能产生可检测到的ASGP-R。转导的ASGP-R对去唾液酸血清类黏蛋白的亲和力低于天然大鼠ASGP-R,并且在表达ASGP-R的克隆中表面受体的数量约为大鼠肝细胞上发现的受体数量的五分之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/387033/040be36affdd/pnas00327-0056-a.jpg

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