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晶状体膜中的主要内在多肽(MIP26K):重组入囊泡及肽抗血清对通道形成活性的抑制作用

Major intrinsic polypeptide (MIP26K) from lens membrane: reconstitution into vesicles and inhibition of channel forming activity by peptide antiserum.

作者信息

Gooden M, Rintoul D, Takehana M, Takemoto L

出版信息

Biochem Biophys Res Commun. 1985 Apr 30;128(2):993-9. doi: 10.1016/0006-291x(85)90145-7.

DOI:10.1016/0006-291x(85)90145-7
PMID:2581574
Abstract

Bovine and human lens membrane, when reconstituted into lipid vesicles containing oxidized cytochrome C, will mediate the transmembrane passage of ascorbate into the vesicles, where the reduction of cytochrome C is measured spectrophotometrically. This channel forming activity is specifically inhibited by antiserum made against a synthetic octapeptide near the C-terminus of MIP26K. Together, these studies describe a direct and more sensitive assay system for measurement of channel-forming activity of MIP26K, and suggest that the C-terminus of this molecule may be particularly important in the regulation of channel formation.

摘要

牛和人晶状体膜在重构到含有氧化型细胞色素C的脂质小泡中时,会介导抗坏血酸跨膜进入小泡,在小泡中通过分光光度法测量细胞色素C的还原情况。这种通道形成活性受到针对MIP26K C端附近合成八肽产生的抗血清的特异性抑制。这些研究共同描述了一种直接且更灵敏的测定系统,用于测量MIP26K的通道形成活性,并表明该分子的C端在通道形成的调节中可能特别重要。

相似文献

1
Major intrinsic polypeptide (MIP26K) from lens membrane: reconstitution into vesicles and inhibition of channel forming activity by peptide antiserum.晶状体膜中的主要内在多肽(MIP26K):重组入囊泡及肽抗血清对通道形成活性的抑制作用
Biochem Biophys Res Commun. 1985 Apr 30;128(2):993-9. doi: 10.1016/0006-291x(85)90145-7.
2
Antisera to synthetic peptides of lens MIP26K (major intrinsic polypeptide): characterization and use as site-specific probes of membrane changes in the aging human lens.针对晶状体MIP26K(主要内在多肽)合成肽的抗血清:特性及其作为衰老人晶状体膜变化位点特异性探针的应用。
Exp Eye Res. 1985 Sep;41(3):415-22. doi: 10.1016/s0014-4835(85)80032-4.
3
Covalent change of major intrinsic polypeptide (MIP26K) of lens membrane during human senile cataractogenesis.人老年性白内障形成过程中晶状体膜主要内在蛋白多肽(MIP26K)的共价变化。
Biochem Biophys Res Commun. 1986 Mar 28;135(3):965-71. doi: 10.1016/0006-291x(86)91022-3.
4
Major intrinsic polypeptide (MIP26K) from human lens membrane: characterization of low-molecular-weight forms in the aging human lens.人晶状体膜中的主要内在多肽(MIP26K):老化人晶状体中低分子量形式的特性
Exp Eye Res. 1986 Oct;43(4):661-7. doi: 10.1016/s0014-4835(86)80032-x.
5
Covalent changes in MIP26K during aging of the human lens membrane.人晶状体膜老化过程中MIP26K的共价变化。
Invest Ophthalmol Vis Sci. 1986 Mar;27(3):443-6.
6
Major intrinsic polypeptide (MIP26K) of the lens membrane: covalent change in an internal sequence during human senile cataractogenesis.晶状体膜的主要内在多肽(MIP26K):人类老年性白内障发生过程中内部序列的共价变化。
Biochem Biophys Res Commun. 1987 Feb 13;142(3):761-6. doi: 10.1016/0006-291x(87)91479-3.
7
Antisera to synthetic peptides of MIP26K as probes of changes in opaque vs. transparent regions within the same human cataractous lens.以MIP26K合成肽抗血清作为探测同一人类白内障晶状体中不透明区与透明区变化的探针。
Exp Eye Res. 1987 Jul;45(1):179-83. doi: 10.1016/s0014-4835(87)80088-x.
8
Is the C-terminal arm of lens gap junction channel protein the channel gate?晶状体间隙连接通道蛋白的C末端臂是通道门吗?
Biochem Biophys Res Commun. 1985 Dec 17;133(2):688-95. doi: 10.1016/0006-291x(85)90959-3.
9
Changes in the major intrinsic polypeptide (MIP26K) during opacification of the Emory mouse lens.埃默里小鼠晶状体浑浊过程中主要内在多肽(MIP26K)的变化。
Exp Eye Res. 1988 Aug;47(2):329-36. doi: 10.1016/0014-4835(88)90015-2.
10
Covalent change in the major intrinsic polypeptide (MIP26K) during cataract development in the streptozotocin-induced diabetic rat.链脲佐菌素诱导的糖尿病大鼠白内障形成过程中主要内在多肽(MIP26K)的共价变化
Curr Eye Res. 1989 Jun;8(6):589-93. doi: 10.3109/02713688908995758.

引用本文的文献

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Pannexin1 and Pannexin2 channels show quaternary similarities to connexons and different oligomerization numbers from each other.Pannexin1 和 Pannexin2 通道与连接子具有四级相似性,并且彼此的寡聚化数量不同。
J Biol Chem. 2010 Aug 6;285(32):24420-31. doi: 10.1074/jbc.M110.115444. Epub 2010 Jun 1.
2
Expression of the gene for main intrinsic polypeptide (MIP): separate spatial distributions of MIP and beta-crystallin gene transcripts in rat lens development.主要内在蛋白(MIP)基因的表达:大鼠晶状体发育过程中MIP和β-晶状体蛋白基因转录本的不同空间分布
J Cell Biol. 1988 Mar;106(3):705-14. doi: 10.1083/jcb.106.3.705.
3
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.
4
Phosphorylation of MP26, a lens junction protein, is enhanced by activators of protein kinase C.MP26(一种晶状体连接蛋白)的磷酸化作用会被蛋白激酶C的激活剂增强。
J Membr Biol. 1989 Feb;107(2):145-55. doi: 10.1007/BF01871720.
5
Channel reconstitution in liposomes and planar bilayers with HPLC-purified MIP26 of bovine lens.利用高效液相色谱法纯化的牛晶状体MIP26在脂质体和平面双分子层中进行通道重建。
J Membr Biol. 1991 Oct;124(1):21-32. doi: 10.1007/BF01871361.
6
Properties of channels reconstituted from the major intrinsic protein of lens fiber membranes.从晶状体纤维细胞膜主要内在蛋白重构的通道特性。
J Gen Physiol. 1990 Sep;96(3):631-64. doi: 10.1085/jgp.96.3.631.
7
The permeability of reconstituted liposomes containing the purified lens fiber cell integral membrane proteins MP20, MP26 and MP70.含有纯化的晶状体纤维细胞整合膜蛋白MP20、MP26和MP70的重构脂质体的渗透性。
J Membr Biol. 1992 Dec;130(3):251-63. doi: 10.1007/BF00240482.
8
Phosphorylation modulates the voltage dependence of channels reconstituted from the major intrinsic protein of lens fiber membranes.磷酸化作用可调节由晶状体纤维细胞膜主要内在蛋白重构的通道的电压依赖性。
J Membr Biol. 1992 Feb;126(1):75-88. doi: 10.1007/BF00233462.