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Low molecular weight subunits associated with the cytochrome b 6 f complexes from spinach and Chlamydomonas reinhardtii.菠菜和莱茵衣藻细胞色素 b6f 复合物的低分子量亚基。
Photosynth Res. 1993 Oct;38(1):73-81. doi: 10.1007/BF00015063.
2
Conservation of lipid functions in cytochrome bc complexes.细胞色素 bc 复合物中脂功能的保护。
J Mol Biol. 2011 Nov 18;414(1):145-62. doi: 10.1016/j.jmb.2011.09.023. Epub 2011 Sep 28.
3
The Q cycle of cytochrome bc complexes: a structure perspective.细胞色素bc复合物的Q循环:结构视角
Biochim Biophys Acta. 2011 Jul;1807(7):788-802. doi: 10.1016/j.bbabio.2011.02.006. Epub 2011 Feb 23.
4
NdhP and NdhQ: two novel small subunits of the cyanobacterial NDH-1 complex.NdhP 和 NdhQ:两种新型的蓝细菌 NDH-1 复合物的小亚基。
Biochemistry. 2011 Feb 22;50(7):1121-4. doi: 10.1021/bi102044b. Epub 2011 Jan 27.
5
Mobility of BtuB and OmpF in the Escherichia coli outer membrane: implications for dynamic formation of a translocon complex.BtuB 和 OmpF 在大肠杆菌外膜中的流动性:对易位子复合物动态形成的影响。
Biophys J. 2010 Dec 15;99(12):3880-6. doi: 10.1016/j.bpj.2010.10.029.
6
Directed epitope delivery across the Escherichia coli outer membrane through the porin OmpF.通过孔蛋白 OmpF 将表位定向递送至大肠杆菌外膜。
Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21412-7. doi: 10.1073/pnas.1010780107. Epub 2010 Nov 22.
7
Cyanobacterial NDH-1 complexes: novel insights and remaining puzzles.蓝藻NDH-1复合体:新见解与遗留谜题
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8
Functional modules and structural basis of conformational coupling in mitochondrial complex I.线粒体复合物 I 构象偶联的功能模块和结构基础。
Science. 2010 Jul 23;329(5990):448-51. doi: 10.1126/science.1191046. Epub 2010 Jul 1.
9
The architecture of respiratory complex I.呼吸复合物 I 的结构。
Nature. 2010 May 27;465(7297):441-5. doi: 10.1038/nature09066.
10
Small single transmembrane domain (STMD) proteins organize the hydrophobic subunits of large membrane protein complexes.小分子单跨膜域(STMD)蛋白组织大膜蛋白复合物的疏水性亚基。
FEBS Lett. 2010 Jun 18;584(12):2516-25. doi: 10.1016/j.febslet.2010.04.021. Epub 2010 Apr 14.

膜蛋白的四重奏:功能先于结构确定。

Membrane proteins in four acts: function precedes structure determination.

机构信息

Department of Biological Sciences, Purdue University, Hall of Structural Biology, 240 Hockmeyer Hall, West Lafayette, IN 47907-1354, USA.

出版信息

Methods. 2011 Dec;55(4):415-20. doi: 10.1016/j.ymeth.2011.11.001. Epub 2011 Nov 10.

DOI:10.1016/j.ymeth.2011.11.001
PMID:22079407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3282554/
Abstract

Studies on four membrane protein systems, which combine information derived from crystal structures and biophysical studies have emphasized, as a precursor to crystallization, demonstration of functional activity. These assays have relied on sensitive spectrophotometric, electrophysiological, and microbiological assays of activity to select purification procedures that lead to functional complexes and with greater likelihood to successful crystallization: (I), Hetero-oligomeric proteins involved in electron transport/proton translocation. (1) Crystal structures of the eight subunit hetero-oligomeric trans-membrane dimeric cytochrome b(6)f complex were obtained from cyanobacteria using a protocol that allowed an analysis of the structure and function of internal lipids at specific intra-membrane, intra-protein sites. Proteolysis and monomerization that inactivated the complex and prevented crystallization was minimized through the use of filamentous cyanobacterial strains that seem to have a different set of membrane-active proteases. (2) An NADPH-quinone oxido-reductase isolated from cyanobacteria contains an expanded set of 17 monotopic and polytopic hetero-subunits. (II) β-Barrel outer membrane proteins (OMPs). High resolution structures of the vitamin B(12) binding protein, BtuB, solved in meso and in surfo, provide the best example of the differences in such structures that were anticipated in the first application of the lipid cubic phase to membrane proteins [1]. A structure of the complex of BtuB with the colicin E3 and E2 receptor binding domain established a "fishing pole" model for outer membrane receptor function in cellular import of nuclease colicins. (III) A modified faster purification procedure contributed to significantly improved resolution (1.83Å) of the universal porin, OmpF, the first membrane protein for which meaningful 3D crystals have been obtained [2]. A crystal structure of the N-terminal translocation domain of colicin E3 complexed to OmpF established the role of OmpF as an import channel for colicin nuclease cytotoxins. (IV) α-Synuclein, associated with the etiology of Parkinson's Disease, is an example of a protein, which is soluble and disordered in solution, but which can assume an ordered predominantly α-helical conformation upon binding to membranes. When subjected in its membrane-bound form to a trans-membrane electrical potential, α-synuclein can form voltage-gated ion channels. Summary of methods to assay functions/activities: (i) sensitive spectrophotometric assay to measure electron transfer activities; (ii) hydrophobic chromatography to deplete lipids, allowing reconstitution with specific lipids for studies on lipid-protein interactions; (iii) microbiological screen to assay high affinity binding of colicin receptor domains to Escherichia coli outer membrane receptors; (iv) electrophysiology/channel analysis (a) to select channel-occluding ligands for co-crystallization with ion channels of OmpF, and (b) to provide a unique description of voltage-gated ion channels of α-synuclein.

摘要

对四个膜蛋白系统的研究,这些系统结合了晶体结构和生物物理研究的信息,强调了在结晶之前展示功能活性的重要性。这些测定依赖于对活性的灵敏分光光度、电生理学和微生物学测定,以选择导致功能复合物的纯化程序,从而提高结晶成功的可能性:(I)参与电子传递/质子转运的异源寡聚蛋白。(1)使用允许在特定的膜内、蛋白内位置分析内部脂质的结构和功能的方案,从蓝细菌中获得了八个亚基异源跨膜二聚体细胞色素 b(6)f 复合物的晶体结构。通过使用丝状蓝细菌菌株,最大限度地减少了蛋白水解和单体化,这些菌株似乎具有不同的一组膜活性蛋白酶,从而使复合物失活并阻止结晶。(2)从蓝细菌中分离出的 NADPH-醌氧化还原酶含有一组扩展的 17 个单拓扑和多拓扑异源亚基。(II)β-桶外膜蛋白 (OMPs)。维生素 B(12)结合蛋白 BtuB 的高分辨率结构,分别在 meso 和 surfo 中得到解决,为这种结构的差异提供了最好的例子,这在脂质立方相首次应用于膜蛋白时就已经预期到了[1]。BtuB 与 colicin E3 和 E2 受体结合域复合物的结构建立了外膜受体在细胞内导入核酸内切酶 colicins 中的功能的“钓鱼竿”模型。(III)改进的更快的纯化程序有助于显著提高分辨率(1.83Å)的通用孔蛋白 OmpF,这是第一个获得有意义的 3D 晶体的膜蛋白[2]。Colicin E3 的 N 端转运结构域与 OmpF 复合物的晶体结构确立了 OmpF 作为 colicin 核酸内切酶细胞毒素进入细胞的入口通道的作用。(IV)与帕金森病病因相关的α-突触核蛋白是一种在溶液中可溶性和无序的蛋白质,但在与膜结合时可以形成有序的主要α-螺旋构象。当以其膜结合形式施加跨膜电势时,α-突触核蛋白可以形成电压门控离子通道。测定功能/活性的方法总结:(i)灵敏的分光光度测定法,用于测量电子转移活性;(ii)疏水性色谱法,耗尽脂质,允许用特定的脂质进行脂质-蛋白相互作用的重建;(iii)微生物筛选,用于测定 colicin 受体结构域与大肠杆菌外膜受体的高亲和力结合;(iv)电生理学/通道分析 (a) 选择与 OmpF 的离子通道共结晶的通道堵塞配体,(b) 提供α-突触核蛋白电压门控离子通道的独特描述。