Transient 2D-IR spectroscopy: Snapshots of the nonequilibrium ensemble during the picosecond conformational transition of a small peptide

被引:142
作者
Bredenbeck, J
Helbing, J
Behrendt, R
Renner, C
Moroder, L
Wachtveitl, J
Hamm, P
机构
[1] Univ Zurich, Inst Phys Chem, CH-8057 Zurich, Switzerland
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Goethe Univ Frankfurt, Inst Phys & Theoret Chem, D-60439 Frankfurt, Germany
关键词
D O I
10.1021/jp034552q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The technique of transient two-dimensional infrared (T2D-IR) spectroscopy is introduced, which extends the advantage of 2D-IR spectroscopy to the investigation of a transient species with picosecond time resolution. The conformational. change of a small cyclic peptide is studied in the amide-I spectral range, which is induced by means of a photoswitch integrated into the peptide backbone. Substantial changes are found in the transient 2D-IR spectra at times when the transient ID spectra show only a minor time dependence, illustrating the information gain accessible from 2D-IR spectroscopy. In contrast to ID spectroscopy, 2D-IR can distinguish between homogeneous and inhomogeneous broadening. The homogeneous contribution to the total width of the amide-I band changes during the course of the conformational transition, a result that is interpreted in terms of the manner in which the peptide samples its conformational space.
引用
收藏
页码:8654 / 8660
页数:7
相关论文
共 38 条
[1]   Versatile small volume closed-cycle flow cell system for transient spectroscopy at high repetition rates [J].
Bredenbeck, J ;
Hamm, P .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2003, 74 (06) :3188-3189
[2]   Picosecond conformational transition and equilibration of a cyclic peptide [J].
Bredenbeck, J ;
Helbing, J ;
Sieg, A ;
Schrader, T ;
Zinth, W ;
Renner, C ;
Behrendt, R ;
Moroder, L ;
Wachtveitl, J ;
Hamm, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6452-6457
[3]   Chromophore-solvent dynamics [J].
Fleming, GR ;
Cho, MH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1996, 47 :109-134
[4]  
Frisch M.J., 2016, Gaussian 16 Revision C. 01. 2016, V16, P01
[5]   Vibrational anharmonicities revealed by coherent two-dimensional infrared spectroscopy [J].
Golonzka, O ;
Khalil, M ;
Demirdöven, N ;
Tokmakoff, A .
PHYSICAL REVIEW LETTERS, 2001, 86 (10) :2154-2157
[6]   Subpicosecond infrared spectroscopy on the photoisomerisation of the protonated Schiff base of all-trans retinal [J].
Hamm, P ;
Zurek, M ;
Roschinger, T ;
Patzelt, H ;
Oesterhelt, DS ;
Zinth, W .
CHEMICAL PHYSICS LETTERS, 1997, 268 (1-2) :180-186
[7]   Noise suppression in femtosecond mid-infrared light sources [J].
Hamm, P ;
Kaindl, RA ;
Stenger, J .
OPTICS LETTERS, 2000, 25 (24) :1798-1800
[8]   Structure of the amide I band of peptides measured by femtosecond nonlinear-infrared spectroscopy [J].
Hamm, P ;
Lim, MH ;
Hochstrasser, RM .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (31) :6123-6138
[9]  
Hamm P, 2001, PRACT SPECTROSC SERI, V26, P273
[10]   Coupling of the amide I modes of the glycine dipeptide [J].
Hamm, P ;
Woutersen, S .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2002, 75 (05) :985-988