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1
Solid-state NMR studies of the membrane-bound closed state of the colicin E1 channel domain in lipid bilayers.脂质双分子层中大肠杆菌素E1通道结构域膜结合封闭状态的固态核磁共振研究。
Protein Sci. 1998 Feb;7(2):342-8. doi: 10.1002/pro.5560070214.
2
Orientational distribution of alpha-helices in the colicin B and E1 channel domains: a one and two dimensional 15N solid-state NMR investigation in uniaxially aligned phospholipid bilayers.大肠杆菌素B和E1通道结构域中α-螺旋的取向分布:在单轴排列的磷脂双分子层中的一维和二维¹⁵N固体核磁共振研究
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3
Effects of anionic lipid and ion concentrations on the topology and segmental mobility of colicin Ia channel domain from solid-state NMR.阴离子脂质和离子浓度对固态核磁共振法测定的大肠菌素Ia通道结构域拓扑结构和片段流动性的影响
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A mechanism for toxin insertion into membranes is suggested by the crystal structure of the channel-forming domain of colicin E1.大肠杆菌素E1通道形成结构域的晶体结构提示了毒素插入细胞膜的一种机制。
Structure. 1997 Mar 15;5(3):443-58. doi: 10.1016/s0969-2126(97)00200-1.
5
Conformational changes of colicin Ia channel-forming domain upon membrane binding: a solid-state NMR study.结合膜时大肠杆菌素Ia通道形成结构域的构象变化:一项固态核磁共振研究。
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Mapping the membrane topology of the closed state of the colicin E1 channel.绘制大肠杆菌素E1通道关闭状态的膜拓扑结构
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7
Constraints imposed by protease accessibility on the trans-membrane and surface topography of the colicin E1 ion channel.蛋白酶可及性对大肠杆菌素E1离子通道跨膜和表面拓扑结构的限制。
Protein Sci. 1992 Dec;1(12):1666-76. doi: 10.1002/pro.5560011215.
8
Specific isotope labeling of colicin E1 and B channel domains for membrane topological analysis by oriented solid-state NMR spectroscopy.通过定向固态核磁共振光谱对大肠杆菌素E1和B通道结构域进行特定同位素标记以进行膜拓扑分析。
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10
Tilted, extended, and lying in wait: the membrane-bound topology of residues Lys-381-Ser-405 of the colicin E1 channel domain.倾斜、伸展并伺机而动:大肠杆菌素E1通道结构域中赖氨酸-381至丝氨酸-405残基的膜结合拓扑结构
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alphaB-crystallin: a hybrid solid-state/solution-state NMR investigation reveals structural aspects of the heterogeneous oligomer.αB-晶状体蛋白:一项混合固态/溶液态核磁共振研究揭示了异质寡聚体的结构特征。
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8
Identifying anisotropic constraints in multiply labeled bacteriorhodopsin by 15N MAOSS NMR: a general approach to structural studies of membrane proteins.通过15N MAOSS NMR鉴定多重标记细菌视紫红质中的各向异性限制:膜蛋白结构研究的通用方法
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Structural studies of apoptosis and ion transport regulatory proteins in membranes.膜中凋亡及离子转运调节蛋白的结构研究
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Assembly of colicin A in the outer membrane of producing Escherichia coli cells requires both phospholipase A and one porin, but phospholipase A is sufficient for secretion.大肠杆菌产生的大肠菌素A在外膜中的组装既需要磷脂酶A和一种孔蛋白,但磷脂酶A对于分泌来说就足够了。
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本文引用的文献

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Complete resolution of the solid-state NMR spectrum of a uniformly 15N-labeled membrane protein in phospholipid bilayers.磷脂双分子层中均匀15N标记的膜蛋白固态核磁共振谱的完全解析。
Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8551-6. doi: 10.1073/pnas.94.16.8551.
2
Orientations of helical peptides in membrane bilayers by solid state NMR spectroscopy.通过固态核磁共振光谱法研究螺旋肽在膜双分子层中的取向
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3
Membrane binding of the colicin E1 channel: activity requires an electrostatic interaction of intermediate magnitude.大肠杆菌素E1通道的膜结合:活性需要中等强度的静电相互作用。
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Characterization of electrostatic and nonelectrostatic components of protein--membrane binding interactions.蛋白质-膜结合相互作用中静电和非静电成分的表征
Biochemistry. 1996 Feb 27;35(8):2717-25. doi: 10.1021/bi951535l.
5
Three-dimensional solid-state NMR spectroscopy of a peptide oriented in membrane bilayers.膜双分子层中定向肽的三维固态核磁共振光谱学。
J Biomol NMR. 1995 Nov;6(3):329-34. doi: 10.1007/BF00197814.
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fd coat protein structure in membrane environments.膜环境中的fd外壳蛋白结构
J Mol Biol. 1993 Oct 5;233(3):447-63. doi: 10.1006/jmbi.1993.1523.
7
Colicin E1 binding to membranes: time-resolved studies of spin-labeled mutants.大肠杆菌素E1与膜的结合:自旋标记突变体的时间分辨研究
Science. 1993 Feb 12;259(5097):960-3. doi: 10.1126/science.8382373.
8
Structure of the membrane-bound form of the pore-forming domain of colicin A: a partial proteolysis and mass spectrometry study.大肠杆菌素A成孔结构域膜结合形式的结构:部分蛋白酶解和质谱研究
Biochemistry. 1993 Dec 21;32(50):13787-94. doi: 10.1021/bi00213a006.
9
Rendering a membrane protein soluble in water: a common packing motif in bacterial protein toxins.使膜蛋白在水中可溶:细菌蛋白毒素中的一种常见堆积基序。
Trends Biochem Sci. 1993 Oct;18(10):391-5. doi: 10.1016/0968-0004(93)90096-6.
10
Uncoupled steps of the colicin A pore formation demonstrated by disulfide bond engineering.通过二硫键工程展示的大肠杆菌素A孔形成的解偶联步骤。
J Biol Chem. 1994 Mar 4;269(9):6332-9.

脂质双分子层中大肠杆菌素E1通道结构域膜结合封闭状态的固态核磁共振研究。

Solid-state NMR studies of the membrane-bound closed state of the colicin E1 channel domain in lipid bilayers.

作者信息

Kim Y, Valentine K, Opella S J, Schendel S L, Cramer W A

机构信息

Department of Chemistry, University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Protein Sci. 1998 Feb;7(2):342-8. doi: 10.1002/pro.5560070214.

DOI:10.1002/pro.5560070214
PMID:9521110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2143909/
Abstract

The colicin E1 channel polypeptide was shown to be organized anisotropically in membranes by solid-state NMR analysis of samples of uniformly 15N-labeled protein in oriented planar phospholipid bilayers. The 190 residue C-terminal colicin E1 channel domain is the largest polypeptide to have been characterized by 15N solid-state NMR spectroscopy in oriented membrane bilayers. The 15N-NMR spectra of the colicin E1 show that: (1) the structure and dynamics are independent of anionic lipid content in both oriented and unoriented samples; (2) assuming the secondary structure of the polypeptide is helical, there are both trans-membrane and in-plane helical segments; (3) trans-membrane helices account for approximately 20-25% of the channel polypeptide, which is equivalent to 38-48 residues of the 190-residue polypeptide. The results of the two-dimensional PISEMA spectrum are interpreted in terms of a single trans-membrane helical hairpin inserted into the bilayer from each channel molecule. These data are also consistent with this helical hairpin being derived from the 38-residue hydrophobic segment near the C-terminus of the colicin E1 channel polypeptide.

摘要

通过对定向平面磷脂双层中均匀15N标记的蛋白质样品进行固态核磁共振分析,发现大肠杆菌素E1通道多肽在膜中呈各向异性排列。190个残基的大肠杆菌素E1通道C端结构域是通过15N固态核磁共振光谱在定向膜双层中表征的最大多肽。大肠杆菌素E1的15N核磁共振光谱表明:(1)在定向和非定向样品中,其结构和动力学均与阴离子脂质含量无关;(2)假设多肽的二级结构为螺旋结构,则存在跨膜螺旋段和面内螺旋段;(3)跨膜螺旋约占通道多肽的20%-25%,相当于190个残基多肽中的38-48个残基。二维PISEMA光谱的结果解释为每个通道分子有一个跨膜螺旋发夹插入双层膜中。这些数据也与该螺旋发夹源自大肠杆菌素E1通道多肽C端附近38个残基的疏水片段一致。