Residue-specific multidimensional IR of cyt-c folding

cyt-c 折叠的残基特异性多维红外光谱

• 批准号: 6899693
• 负责人: CASEY H LONDERGAN
• 金额: $ 4.83万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-07-01 至 2006-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6899693
• 关键词: carbon; cytochrome c; infrared spectrometry; molecular dynamics; oxygen; postdoctoral investigator; protein folding; protein structure; stable isotope

DESCRIPTION (provided by applicant): Three-pulse two-dimensional infrared spectroscopy (2D-IR) is a technique which is capable of resolving molecular structure (via angles between transition dipoles and vibrational coupling constants), dynamics (via variable time delays and homogeneous line shapes), and structural distributions on time scales down to femtoseconds. Cytochrome-c is a well-studied, fast-folding heme protein: in cyt-c folding studies, misfolded and ligand-exchanged structures have been implicated in a heterogeneous dynamic structural distribution associated with the folding events. It is proposed here to use 2D-IR to resolve the equilibrium and dynamic (folding) structural distributions of the peptide chain of cyt-c near the heme. Isotopic labeling of Met80 (a native heme ligand) and Phe82 residues with 13C/180 and 13C/160 carbonyls will be used to spectrally isolate the amide-I vibrations of this part of the chain which is close to the heine. 2D-IR of the labeled residues, which yields the distances and angles between them, will be used to determine the equilibrium structural distribution of native-sequence cyt-c and the perturbed equilibrium distributions of Phe82 mutants. After integration of a visible trigger pulse into the existing three-pulse infrared optical bench, denatured CO-heme cyt-c will be photolyzed to initiate folding to the native structure. 2D-IR of the labeled residues will be used to monitor the time-evolving structural distribution associated with cyt-c folding.

描述(由申请人提供)： 三脉冲二维红外光谱(2D-IR)是一种能够分辨分子结构(通过跃迁偶极子和振动耦合常数之间的夹角)、动力学(通过可变的时间延迟和均匀的线形)以及结构在时间尺度上的分布(精确到飞秒)的技术。细胞色素-c是一种研究广泛的快速折叠的血红素蛋白：在细胞色素-c折叠研究中，错误折叠和配体交换结构与折叠事件相关的异质动态结构分布有关。本文建议使用2D-IR来解析Cyt-c在血红素附近的肽链的平衡和动态(折叠)结构分布。Met80(一种天然的血红素配体)和Phe82残基与13C/180和13C/160羰基的同位素标记将用于光谱分离靠近Heine的这部分链的酰胺-I振动。标记残基的2D-IR得到它们之间的距离和角度，将用于确定天然序列cyt-c的平衡结构分布和Phe82突变体的扰动平衡分布。在现有的三脉冲红外光学实验台上集成了可见触发脉冲后，变性的CO-血红素Cyt-c将被光解，启动折叠到自然结构。标记残基的2D-IR将用于监测与Cyt-c折叠相关的随时间演变的结构分布。