Advances in spectroscopic methods for biological crystals. 2. Raman spectroscopy

被引:46
作者
Carpentier, Philippe
Royant, Antoine
Ohana, Jeremy
Bourgeois, Dominique
机构
[1] Univ Grenoble 1, Inst Biol Struct Jean Pierre Ebel, Cristallog & Cristallogenese Prot Lab, CEA,CNRS, F-38027 Grenoble, France
[2] European Synchrotron Radiat Facil, F-38043 Grenoble, France
来源
JOURNAL OF APPLIED CRYSTALLOGRAPHY | 2007年 / 40卷
关键词
D O I
10.1107/S0021889807044202
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Raman microspectrophotometer is described that allows the spectroscopic investigation of protein crystals under exactly the same conditions as those used for X-ray data collection. The concept is based on the integration of the Raman excitation/collection optics into a microspectrophotometer built around a single-axis diffractometer and a cooling device. It is shown that Raman spectra of outstanding quality can be recorded from crystallized macromolecules under non-resonant conditions. It is proposed that equipment developed in the context of macromolecular cryocrystallography, such as commonly used cryoloops, can be advantageously used to improve the quality of Raman spectra. In a few examples, it is shown that Raman microspectrophotometry provides crucial complementary information to X-ray crystallography, e. g. identifying the chemical nature of unknown features discovered in electron-density maps, or following ligand-binding kinetics in biological crystals. The feasibility of 'online' Raman measurements performed directly on the ESRF macromolecular crystallography beamlines has been investigated and constitutes a promising perspective for the routine implementation of combined spectroscopic and crystallographic methods. In crystallo Raman spectroscopy efficiently complements absorption/fluorescence microspectrophotometry for the study of biological crystals and opens up new avenues for difficult structural projects with mechanistic perspectives in the field of protein crystallography.
引用
收藏
页码:1113 / 1122
页数:10
相关论文
共 52 条
[1]   Comparing protein-ligand interactions in solution and single crystals by Raman spectroscopy [J].
Altose, MD ;
Zheng, YG ;
Dong, J ;
Palfey, BA ;
Carey, PR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3006-3011
[2]   Raman, polarized Raman and ultraviolet resonance Raman spectroscopy of nucleic acids and their complexes [J].
Benevides, JM ;
Overman, SA ;
Thomas, GJ .
JOURNAL OF RAMAN SPECTROSCOPY, 2005, 36 (04) :279-299
[3]   The catalytic pathway of horseradish peroxidase at high resolution [J].
Berglund, GI ;
Carlsson, GH ;
Smith, AT ;
Szöke, H ;
Henriksen, A ;
Hajdu, J .
NATURE, 2002, 417 (6887) :463-468
[4]  
Blake C C, 1968, Adv Protein Chem, V23, P59, DOI 10.1016/S0065-3233(08)60400-3
[5]  
Blundell T. L., 1976, Protein crystallography
[6]   Advances in kinetic protein crystallography [J].
Bourgeois, D ;
Royant, A .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2005, 15 (05) :538-547
[7]   A microspectrophotometer for UV-visible absorption and fluorescence studies of protein crystals [J].
Bourgeois, D ;
Vernede, X ;
Adam, V ;
Fioravanti, E ;
Ursby, T .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2002, 35 :319-326
[8]   Raman crystallography and other biochemical applications of Raman microscopy [J].
Carey, Paul R. .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 2006, 57 :527-554
[9]   Following ligand binding and ligand reactions in proteins via Raman crystallography [J].
Carey, PR ;
Dong, J .
BIOCHEMISTRY, 2004, 43 (28) :8885-8893
[10]   Raman spectroscopy, the sleeping giant in structural biology, awakes [J].
Carey, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26625-26628