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牛晶状体纤维膜的主要内在蛋白(MIP):基于cDNA克隆的表征与结构

The major intrinsic protein (MIP) of the bovine lens fiber membrane: characterization and structure based on cDNA cloning.

作者信息

Gorin M B, Yancey S B, Cline J, Revel J P, Horwitz J

出版信息

Cell. 1984 Nov;39(1):49-59. doi: 10.1016/0092-8674(84)90190-9.

Abstract

Synthetic oligonucleotide probes have been used to identify two overlapping cDNA clones that represent the entire coding region of the mRNA for the major intrinsic protein (MIP) of bovine lens cell membrane. Hybridization studies indicate that bovine MIP is encoded by a single-copy gene. The cDNA hybridizes to the rat genome, but MIP mRNA is not detected in rat liver. Analysis of the deduced amino acid sequence provides support for the potential role of MIP as a junctional protein. The structure predicted for MIP suggests that it traverses the lipid bilayer six times with both carboxy and amino termini on the cytoplasmic side, and that it has at least one amphiphilic transmembrane segment, as expected if the protein were to participate in the formation of an aqueous channel.

摘要

合成寡核苷酸探针已被用于鉴定两个重叠的cDNA克隆,它们代表牛晶状体细胞膜主要内在蛋白(MIP)的mRNA的完整编码区。杂交研究表明,牛MIP由单拷贝基因编码。该cDNA与大鼠基因组杂交,但在大鼠肝脏中未检测到MIP mRNA。对推导的氨基酸序列的分析为MIP作为连接蛋白的潜在作用提供了支持。预测的MIP结构表明,它在脂质双层中穿膜六次,羧基和氨基末端都在细胞质一侧,并且它至少有一个两亲性跨膜片段,这与该蛋白参与形成水通道的预期一致。

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