内吞作用
等位基因
家族性高胆固醇血症
低密度脂蛋白受体
LRP1B型
突变体
内化
低密度脂蛋白
细胞生物学
受体介导的内吞作用
基因座(遗传学)
受体
遗传学
基因
分子生物学
生物
脂蛋白
生物化学
胆固醇
作者
Joseph L. Goldstein,Sandip K. Basu,Michael S. Brown
出处
期刊:Methods in Enzymology
日期:1983-01-01
卷期号:: 241-260
被引量:1629
标识
DOI:10.1016/0076-6879(83)98152-1
摘要
Studies of the cell surface binding, internalization, and metabolism of low-density lipoprotein (LDL) in cultured cells have provided useful information regarding the general aspects of receptor-mediated endocytosis. The study of the LDL receptor has been facilitated by analysis of mutant fibroblasts obtained from human subjects with disorders of cholesterol metabolism. The most informative cells, obtained from patients with familial hypercholesterolemia (FH), have defects in the gene encoding the LDL receptor. The existence of three classes of mutant alleles at the LDL receptor locus has been deduced on the basis of genetic and kinetic data. One of these alleles specifies a receptor that is unable to bind LDL. The second type of allele specifies a receptor that can bind small amounts of LDL; and the third type of allele specifies a receptor that can bind LDL but cannot be incorporated into coated pits and hence cannot carry the LDL into the cell. The first two alleles are common among FH patients, whereas the third allele is extremely rare.
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