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含有 GpATM 二聚化模体的合成跨膜多肽的取向和动力学。

Orientation and dynamics of synthetic transbilayer polypeptides containing GpATM dimerization motifs.

机构信息

Department of Physics and Physical Oceanography, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada.

Department of Biochemistry, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada; Department of Physics and Physical Oceanography, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada.

出版信息

Biophys J. 2011 Feb 2;100(3):656-664. doi: 10.1016/j.bpj.2010.12.3725.

Abstract

Deuterium NMR spectroscopy was used to study how the positioning of a dimerization motif within a transbilayer polypeptide influences its orientation and dynamics in bilayers. Three polypeptide variants comprising glycophorin A transmembrane (GpATM) dimerization motifs incorporated into lysine-terminated poly-leucine-alanine helices were mixed into 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine multilamellar vesicles. The variants differed in orientation of the motif segment around the helix axis with respect to the peptide ends. Polypeptides were labeled with methyl-deuterated alanines at positions that were identically situated relative to the peptide ends (Ala-20 and Ala-22) and at two positions within the motif. An analysis of quadrupole splittings revealed similar tilts and orientations of the peptide ends for all three variants, suggesting that average orientations were dominated by interactions at the bilayer surface. For one variant, however, fast orientational fluctuations about the helix axis were significantly smaller. This may indicate some perturbation of peptide dynamics and conformation by interactions that are sensitive to the motif orientation relative to the peptide ends. For the variant that displayed distinct dynamics, one orientation consistent with observed splittings corresponded to the motif being situated such that its two glycines were particularly accessible to adjacent peptides.

摘要

利用氘核核磁共振波谱研究了跨膜多肽二聚化模体在双分子层中的定位如何影响其在双分子层中的取向和动力学。将三种包含糖蛋白 A 跨膜(GpATM)二聚化模体的多肽变体掺入赖氨酸终止的聚亮氨酸-丙氨酸螺旋中,混合到 1-棕榈酰-2-油酰-sn-甘油-3-磷酸胆碱多层囊泡中。这些变体在模体片段相对于肽末端围绕螺旋轴的取向方面存在差异。用甲基氘代丙氨酸标记多肽,这些位置相对于肽末端(Ala-20 和 Ala-22)和模体中的两个位置保持相同。对四极分裂的分析表明,所有三种变体的肽末端具有相似的倾斜和取向,表明平均取向主要由双层表面的相互作用决定。然而,对于一种变体,关于螺旋轴的快速取向波动明显较小。这可能表明肽动力学和构象受到与肽末端相对的模体取向的相互作用的一些干扰。对于显示出不同动力学的变体,与观察到的分裂相对应的一种取向表明,该模体的两个甘氨酸特别容易与相邻的肽相互作用。

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1
Lipid-modulated sequence-specific association of glycophorin A in membranes.
Biophys J. 2010 Jul 7;99(1):284-92. doi: 10.1016/j.bpj.2010.04.005.
2
Driving forces for transmembrane alpha-helix oligomerization.
Biophys J. 2010 Jul 7;99(1):227-37. doi: 10.1016/j.bpj.2010.03.071.
3
Cell signaling by receptor tyrosine kinases.
Cell. 2010 Jun 25;141(7):1117-34. doi: 10.1016/j.cell.2010.06.011.
4
Order parameters of a transmembrane helix in a fluid bilayer: case study of a WALP peptide.
Biophys J. 2010 May 19;98(9):1864-72. doi: 10.1016/j.bpj.2010.01.016.
5
Orientation and dynamics of transmembrane peptides: the power of simple models.
Eur Biophys J. 2010 Mar;39(4):609-21. doi: 10.1007/s00249-009-0567-1. Epub 2009 Dec 18.
6
Alpha-helical transmembrane peptides: a "divide and conquer" approach to membrane proteins.
Chem Phys Lipids. 2010 Jan;163(1):1-26. doi: 10.1016/j.chemphyslip.2009.07.009.
7
Orientation and dynamics of peptides in membranes calculated from 2H-NMR data.
Biophys J. 2009 Apr 22;96(8):3223-32. doi: 10.1016/j.bpj.2009.02.040.
8
The dynamic orientation of membrane-bound peptides: bridging simulations and experiments.
Biophys J. 2007 Dec 15;93(12):4278-88. doi: 10.1529/biophysj.107.113043. Epub 2007 Aug 24.
9
Role of receptor tyrosine kinase transmembrane domains in cell signaling and human pathologies.
Biochemistry. 2006 May 23;45(20):6241-51. doi: 10.1021/bi060609y.

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