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人载脂蛋白B - 100:克隆、肝脏信使核糖核酸分析以及该基因在2号染色体上的定位

Human apolipoprotein B-100: cloning, analysis of liver mRNA, and assignment of the gene to chromosome 2.

作者信息

Law S W, Lackner K J, Hospattankar A V, Anchors J M, Sakaguchi A Y, Naylor S L, Brewer H B

出版信息

Proc Natl Acad Sci U S A. 1985 Dec;82(24):8340-4. doi: 10.1073/pnas.82.24.8340.

Abstract

Human apolipoprotein B-100 (apo B-100) is the major apolipoprotein of low density lipoproteins and the principal ligand for interaction with the low density lipoprotein receptor. The human apo B-100 gene has been inserted into a lambda gt-11 expression vector, and the apo B-100 cDNA clones have been identified by screening with a monospecific apo B-100 antiserum, by screening with synthetic oligonucleotides based on the amino acid sequence of peptides isolated from apo B-100, and by immunoblot analysis of the expressed protein with a monoclonal antibody to apo B-100. The complete nucleotide and derived-amino acid sequence of a 1.7-kilobase cDNA clone of apo B-100 was determined. The 560-amino acid residues of apo B-100 contain no unique linear or repeating sequences of amino acids. The computer-predicted conformation of the apo B-100 protein contains segments of helical structure; however, a large portion of the protein is organized into beta-structure. The beta-structure may be important in lipid-apo B-100 interactions in low density lipoprotein and may contribute to the insolubility of delipidated apo B-100 in aqueous buffers. RNA blot hybridization analysis of liver mRNA utilizing a Nco I/HindIII apo B-100 cDNA probe revealed that the apo B-100 mRNA is 15-18 kilobases long, which is of sufficient size to code for a 250-387 kDa apolipoprotein, the proposed molecular size of delipidated plasma apo B-100. The gene for human apo B-100 has been localized to chromosome 2 by filter hybridization of human-mouse somatic cell hybrids utilizing a 400-base-pair Nco I/HindIII apo B-100 cDNA probe. This location is in contrast to the low density lipoprotein receptor that has been localized to chromosome 19. The cloning of human apo B-100 has provided new insights into the structure and physicochemical properties of apo B-100 and will facilitate studies on the factors modulating apo B-100 biosynthesis and the expression of the apo B-100 gene in patients with dyslipoproteinemias.

摘要

人载脂蛋白B - 100(apo B - 100)是低密度脂蛋白的主要载脂蛋白,也是与低密度脂蛋白受体相互作用的主要配体。人apo B - 100基因已被插入λgt - 11表达载体中,通过用单特异性apo B - 100抗血清筛选、用基于从apo B - 100分离的肽段氨基酸序列的合成寡核苷酸筛选以及用针对apo B - 100的单克隆抗体对表达蛋白进行免疫印迹分析,已鉴定出apo B - 100 cDNA克隆。测定了一个1.7千碱基的apo B - 100 cDNA克隆的完整核苷酸和推导氨基酸序列。apo B - 100的560个氨基酸残基不包含独特的线性或重复氨基酸序列。计算机预测的apo B - 100蛋白构象包含螺旋结构片段;然而,该蛋白的大部分被组织成β结构。β结构可能在低密度脂蛋白中脂质与apo B - 100的相互作用中起重要作用,并且可能导致脱脂apo B - 100在水性缓冲液中不溶。利用Nco I/HindIII apo B - 100 cDNA探针进行的肝脏mRNA的RNA印迹杂交分析表明,apo B - 100 mRNA长15 - 18千碱基,其大小足以编码一种250 - 387 kDa的载脂蛋白,这是脱脂血浆apo B - 100的推测分子大小。利用400碱基对的Nco I/HindIII apo B - 100 cDNA探针,通过人 - 小鼠体细胞杂种的滤膜杂交,已将人apo B - 100基因定位到第2号染色体。这个位置与已定位到第19号染色体的低密度脂蛋白受体相反。人apo B - 100的克隆为apo B - 100的结构和物理化学性质提供了新的见解,并将有助于研究调节apo B - 100生物合成的因素以及血脂异常患者中apo B - 100基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5855/390911/c91d0de286b2/pnas00364-0077-a.jpg

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