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使用红外-紫外双共振光谱和密度泛函理论计算对气相肽的酰胺I光谱图进行评估。

Assessment of amide I spectroscopic maps for a gas-phase peptide using IR-UV double-resonance spectroscopy and density functional theory calculations.

作者信息

Carr J K, Zabuga A V, Roy S, Rizzo T R, Skinner J L

机构信息

Department of Chemistry and Theoretical Chemistry Institute, University of Wisconsin, Madison, Wisconsin 53706, USA.

Laboratoire de Chimie Physique Moleculaire, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LCPM, Station 6, CH-1015 Lausanne, Switzerland.

出版信息

J Chem Phys. 2014 Jun 14;140(22):224111. doi: 10.1063/1.4882059.

Abstract

The spectroscopy of amide I vibrations has become a powerful tool for exploring protein structure and dynamics. To help with spectral interpretation, it is often useful to perform molecular dynamics (MD) simulations. To connect spectroscopic experiments to simulations in an efficient manner, several researchers have proposed "maps," which relate observables in classical MD simulations to quantum spectroscopic variables. It can be difficult to discern whether errors in the theoretical results (compared to experiment) arise from inaccuracies in the MD trajectories or in the maps themselves. In this work, we evaluate spectroscopic maps independently from MD simulations by comparing experimental and theoretical spectra for a single conformation of the α-helical model peptide Ac-Phe-(Ala)5-Lys-H(+) in the gas phase. Conformation-specific experimental spectra are obtained for the unlabeled peptide and for several singly and doubly (13)C-labeled variants using infrared-ultraviolet double-resonance spectroscopy, and these spectra are found to be well-modeled by density functional theory (DFT) calculations at the B3LYP/6-31G** level. We then compare DFT results for the deuterated and (13)C(18)O-labeled peptide with those from spectroscopic maps developed and used previously by the Skinner group. We find that the maps are typically accurate to within a few cm(-1) for both frequencies and couplings, having larger errors only for the frequencies of terminal amides.

摘要

酰胺 I 振动光谱已成为探索蛋白质结构和动力学的有力工具。为了辅助光谱解释,进行分子动力学(MD)模拟通常很有用。为了以高效的方式将光谱实验与模拟联系起来,几位研究人员提出了“图谱”,它将经典 MD 模拟中的可观测量与量子光谱变量联系起来。很难辨别理论结果(与实验相比)中的误差是源于 MD 轨迹的不准确还是图谱本身的不准确。在这项工作中,我们通过比较气相中 α 螺旋模型肽 Ac-Phe-(Ala)5-Lys-H(+)单一构象的实验光谱和理论光谱,独立于 MD 模拟评估光谱图谱。使用红外 - 紫外双共振光谱获得了未标记肽以及几种单重和双重(13)C 标记变体的构象特异性实验光谱,并且发现这些光谱在 B3LYP/6 - 31G** 水平上通过密度泛函理论(DFT)计算得到了很好的模拟。然后我们将氘代和(13)C(18)O 标记肽的 DFT 结果与 Skinner 小组之前开发和使用的光谱图谱结果进行比较。我们发现,对于频率和耦合,这些图谱通常精确到几厘米(-1)以内,仅在末端酰胺频率上有较大误差。

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