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分子动力学模拟预测强啡肽A(1-17)螺旋区域在二肉豆蔻酰磷脂酰胆碱双层膜中呈倾斜取向。

Molecular dynamics simulations predict a tilted orientation for the helical region of dynorphin A(1-17) in dimyristoylphosphatidylcholine bilayers.

作者信息

Sankararamakrishnan R, Weinstein H

机构信息

Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York University, New York, New York 10029, USA.

出版信息

Biophys J. 2000 Nov;79(5):2331-44. doi: 10.1016/S0006-3495(00)76479-4.

Abstract

The structural properties of the endogenous opioid peptide dynorphin A(1-17) (DynA), a potential analgesic, were studied with molecular dynamics simulations in dimyristoylphosphatidylcholine bilayers. Starting with the known NMR structure of the peptide in dodecylphosphocholine micelles, the N-terminal helical segment of DynA (encompassing residues 1-10) was initially inserted in the bilayer in a perpendicular orientation with respect to the membrane plane. Parallel simulations were carried out from two starting structures, systems A and B, that differ by 4 A in the vertical positioning of the peptide helix. The complex consisted of approximately 26,400 atoms (dynorphin + 86 lipids + approximately 5300 waters). After >2 ns of simulation, which included >1 ns of equilibration, the orientation of the helical segment of DynA had undergone a transition from parallel to tilted with respect to the bilayer normal in both the A and B systems. When the helix axis achieved a approximately 50 degrees angle with the bilayer normal, it remained stable for the next 1 ns of simulation. The two simulations with different starting points converged to the same final structure, with the helix inserted in the bilayer throughout the simulations. Analysis shows that the tilted orientation adopted by the N-terminal helix is due to specific interactions of residues in the DynA sequence with phospholipid headgroups, water, and the hydrocarbon chains. Key elements are the "snorkel model"-type interactions of arginine side chains, the stabilization of the N-terminal hydrophobic sequence in the lipid environment, and the specific interactions of the first residue, Tyr. Water penetration within the bilayer is facilitated by the immersed DynA, but it is not uniform around the surface of the helix. Many water molecules surround the arginine side chains, while water penetration near the helical surface formed by hydrophobic residues is negligible. A mechanism of receptor interaction is proposed for DynA, involving the tilted orientation observed from these simulations of the peptide in the lipid bilayer.

摘要

采用分子动力学模拟方法,在二肉豆蔻酰磷脂酰胆碱双层膜中研究了内源性阿片肽强啡肽A(1 - 17)(DynA)(一种潜在的镇痛药)的结构特性。从该肽在十二烷基磷酸胆碱胶束中的已知核磁共振结构出发,DynA的N端螺旋片段(包含1 - 10位残基)最初以相对于膜平面垂直的方向插入双层膜中。从两个起始结构(系统A和B)进行平行模拟,这两个结构在肽螺旋的垂直定位上相差4 Å。该复合物由约26,400个原子组成(强啡肽 + 86个脂质 + 约5300个水分子)。经过>2 ns的模拟(包括>1 ns的平衡过程),在A和B系统中,DynA螺旋片段的方向都经历了从与双层膜法线平行到倾斜的转变。当螺旋轴与双层膜法线形成约50度角时,在接下来的1 ns模拟中它保持稳定。两个不同起始点的模拟收敛到相同的最终结构,在整个模拟过程中螺旋都插入双层膜中。分析表明,N端螺旋所采用的倾斜方向是由于DynA序列中的残基与磷脂头部基团、水和烃链之间的特定相互作用。关键因素包括精氨酸侧链的“通气管模型”型相互作用、脂质环境中N端疏水序列的稳定以及第一个残基酪氨酸的特定相互作用。DynA促进了双层膜内的水渗透,但在螺旋表面周围并不均匀。许多水分子围绕着精氨酸侧链,而由疏水残基形成的螺旋表面附近的水渗透可以忽略不计。针对DynA提出了一种受体相互作用机制,涉及从这些脂质双层膜中肽的模拟观察到的倾斜方向。

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