Peptide mapping by limited proteolysis in sodium dodecyl sulfate of the main intrinsic polypeptides isolated from human and bovine lens plasma membranes.
作者信息
Horwitz J, Wong M M
出版信息
Biochim Biophys Acta. 1980 Mar 26;622(1):134-43. doi: 10.1016/0005-2795(80)90165-8.
PMID:6988013
Abstract
摘要
相似文献
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Peptide mapping by limited proteolysis in sodium dodecyl sulfate of the main intrinsic polypeptides isolated from human and bovine lens plasma membranes.通过在十二烷基硫酸钠中进行有限蛋白酶解对从人及牛晶状体质膜中分离出的主要内在多肽进行肽图谱分析。
Biochim Biophys Acta. 1980 Mar 26;622(1):134-43. doi: 10.1016/0005-2795(80)90165-8.
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Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.在十二烷基硫酸钠中通过有限蛋白酶解进行肽图谱分析并通过凝胶电泳进行分析。
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Heat induced aggregation of the sodium dodecyl sulfate-solubilized main intrinsic polypeptide isolated from bovine lens plasma membrane.
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Probing the subunit structure of cow anterior lens capsule with the detergent, sodium dodecyl sulfate.用去污剂十二烷基硫酸钠探究牛晶状体前囊膜的亚基结构。
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Some properties of lens plasma membrane polypeptides isolated from normal human lenses.
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Limited proteolysis of bovine lens alpha-crystallin by calpain, a Ca2+-dependent cysteine proteinase, isolated from the same tissue.从同一组织中分离出的钙蛋白酶（一种依赖钙离子的半胱氨酸蛋白酶）对牛晶状体α-晶体蛋白进行有限的蛋白水解。
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Bovine lens 23, 21 and 19 kDa intrinsic membrane proteins have an identical amino-terminal amino acid sequence.牛晶状体23kDa、21kDa和19kDa内在膜蛋白具有相同的氨基末端氨基酸序列。
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Peptide mapping in one dimension by limited proteolysis of sodium dodecyl sulfate-solubilized proteins.通过对十二烷基硫酸钠增溶蛋白进行有限蛋白酶解实现一维肽图谱分析。
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Characterization of three forms of rabbit microsomal cytochrome P-450 by peptide mapping utilizing limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.利用十二烷基硫酸钠中的有限蛋白酶解进行肽图谱分析并通过凝胶电泳分析，对兔微粒体细胞色素P-450的三种形式进行表征。
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State of association of band 3 protein from bovine erythrocyte membrane in nonionic detergent.牛红细胞膜带3蛋白在非离子去污剂中的缔合状态
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引用本文的文献
1
Overview of the Lens.晶状体概述。
Prog Mol Biol Transl Sci. 2015;134:119-27. doi: 10.1016/bs.pmbts.2015.04.006. Epub 2015 May 27.
2
The major polypeptide (MIP) of lens fiber junctions and its synthesis in cultured differentiating lens epithelial cells.晶状体纤维连接的主要多肽（MIP）及其在培养的分化晶状体上皮细胞中的合成。
Biophys Struct Mech. 1982;9(2):95-101. doi: 10.1007/BF00539107.
3
On the structural organization of isolated bovine lens fiber junctions.关于分离的牛晶状体纤维连接的结构组织
J Cell Biol. 1982 Apr;93(1):175-89. doi: 10.1083/jcb.93.1.175.
4
Immunocytochemical localization of the lens main intrinsic polypeptide (MIP26) in communicating junctions.晶状体主要内在多肽（MIP26）在通讯连接中的免疫细胞化学定位。
J Cell Biol. 1982 Jan;92(1):213-20. doi: 10.1083/jcb.92.1.213.
5
Arrangement of MP26 in lens junctional membranes: analysis with proteases and antibodies.MP26在晶状体连接膜中的排列：蛋白酶和抗体分析
J Membr Biol. 1983;74(3):217-28. doi: 10.1007/BF02332125.
6
Comparative analysis of the major polypeptides from liver gap junctions and lens fiber junctions.肝脏缝隙连接和晶状体纤维连接主要多肽的比较分析。
J Cell Biol. 1982 Jan;92(1):53-9. doi: 10.1083/jcb.92.1.53.
7
Phosphorylation of lens fiber cell membrane proteins.晶状体纤维细胞膜蛋白的磷酸化
Proc Natl Acad Sci U S A. 1985 Feb;82(3):653-7. doi: 10.1073/pnas.82.3.653.
8
Junctions between lens fiber cells are labeled with a monoclonal antibody shown to be specific for MP26.晶状体纤维细胞之间的连接用一种单克隆抗体标记，该抗体已被证明对MP26具有特异性。
J Cell Biol. 1985 Jan;100(1):216-25. doi: 10.1083/jcb.100.1.216.
9
The structural organization and protein composition of lens fiber junctions.晶状体纤维连接的结构组织和蛋白质组成。
J Cell Biol. 1989 Jun;108(6):2255-75. doi: 10.1083/jcb.108.6.2255.
10
Electron microscopic observations of reconstituted proteoliposomes with the purified major intrinsic membrane protein of eye lens fibers.对含有纯化的晶状体纤维主要内在膜蛋白的重组蛋白脂质体的电子显微镜观察。
J Cell Biol. 1987 Oct;105(4):1679-89. doi: 10.1083/jcb.105.4.1679.
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