Single-molecule fluorescence spectroscopy in (bio)catalysis

被引:116
作者
Roeffaers, Maarten B. J.
De Cremer, Gert
Uji-i, Hiroshi
Muls, Benlot
Sels, Bert F.
Jacobs, Pierre A.
De Schryver, Frans C.
De Vos, Dirk E.
Hofkens, Johan
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Dept Microbial & Mol Syst, B-3001 Louvain, Belgium
[2] Katholieke Univ Leuven, Dept Chem, B-3001 Louvain, Belgium
[3] Catholic Univ Louvain, Dept Chem, B-1348 Louvain, Belgium
关键词
D O I
10.1073/pnas.0610755104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ever-improving time and space resolution and molecular detection sensitivity of fluorescence microscopy offer unique opportunities to deepen our insights into the function of chemical and biological catalysts. Because single-molecule microscopy allows for counting the turnover events one by one, one can map the distribution of the catalytic activities of different sites in solid heterogeneous catalysts, or one can study time-dependent activity fluctuations of individual sites in enzymes or chemical catalysts. By experimentally monitoring individuals rather than populations, the origin of complex behavior, e.g., in kinetics or in deactivation processes, can be successfully elucidated. Recent progress of temporal and spatial resolution in single-molecule fluorescence microscopy is discussed in light of its impact on catalytic assays. Key concepts are illustrated regarding the use of fluorescent reporters in catalytic reactions. Future challenges comprising the integration of other techniques, such as diffraction, scanning probe, or vibrational methods in single-molecule fluorescence spectroscopy are suggested.
引用
收藏
页码:12603 / 12609
页数:7
相关论文
共 86 条
[1]   Nanoscale vibrational analysis of single-walled carbon nanotubes [J].
Anderson, N ;
Hartschuh, A ;
Cronin, S ;
Novotny, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (08) :2533-2537
[2]   Enhancement and quenching of single-molecule fluorescence [J].
Anger, P ;
Bharadwaj, P ;
Novotny, L .
PHYSICAL REVIEW LETTERS, 2006, 96 (11)
[3]   Recent progress in ultrafast X-ray diffraction [J].
Bargheer, M ;
Zhavoronkov, N ;
Woerner, M ;
Elsaesser, T .
CHEMPHYSCHEM, 2006, 7 (04) :783-792
[4]   LIGAND-ACCELERATED CATALYSIS [J].
BERRISFORD, DJ ;
BOLM, C ;
SHARPLESS, KB .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (10) :1059-1070
[5]   NEAR-FIELD OPTICS - MICROSCOPY, SPECTROSCOPY, AND SURFACE MODIFICATION BEYOND THE DIFFRACTION LIMIT [J].
BETZIG, E ;
TRAUTMAN, JK .
SCIENCE, 1992, 257 (5067) :189-195
[6]   Imaging intracellular fluorescent proteins at nanometer resolution [J].
Betzig, Eric ;
Patterson, George H. ;
Sougrat, Rachid ;
Lindwasser, O. Wolf ;
Olenych, Scott ;
Bonifacino, Juan S. ;
Davidson, Michael W. ;
Lippincott-Schwartz, Jennifer ;
Hess, Harald F. .
SCIENCE, 2006, 313 (5793) :1642-1645
[7]   Isomerization and hydrocracking of heptane over bimetallic bifunctional PtPd/H-beta and PtPd/USY zeolite catalysts [J].
Blomsma, E ;
Martens, JA ;
Jacobs, PA .
JOURNAL OF CATALYSIS, 1997, 165 (02) :241-248
[8]   Photoselective adaptive femtosecond quantum control in the liquid phase [J].
Brixner, T ;
Damrauer, NH ;
Niklaus, P ;
Gerber, G .
NATURE, 2001, 414 (6859) :57-60
[9]   Luminescent sensors and switches in the early 21st century [J].
Callan, JF ;
de Silva, AP ;
Magri, DC .
TETRAHEDRON, 2005, 61 (36) :8551-8588
[10]   Host-guest antenna materials [J].
Calzaferri, G ;
Huber, S ;
Maas, H ;
Minkowski, C .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (32) :3732-3758