Branching out of single-molecule fluorescence spectroscopy: Challenges for chemistry and influence on biology

被引:204
作者
Tinnefeld, P [1 ]
Sauer, M [1 ]
机构
[1] Univ Bielefeld, Fac Phys, D-33615 Bielefeld, Germany
关键词
conformational dynamics; electron transfer; fluorescent labels; FRET (fluorescence resonance energy transfer); single-molecule spectroscopy;
D O I
10.1002/anie.200300647
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Figure Presented) In the last decade emerging single-molecule fluorescence-spectroscopy tools have been developed and adapted to analyze individual molecules under various conditions. Single-molecule-sensitive optical techniques are now well established and help to increase our understanding of complex problems in different disciplines ranging from materials science to cell biology. Previous dreams, such as the monitoring of the motility and structural changes of single motor proteins in living cells or the detection of single-copy genes and the determination of their distance from polymerase molecules in transcription factories in the nucleus of a living cell, no longer constitute unsolvable problems. In this Review we demonstrate that single-molecule fluorescence spectroscopy has become an independent discipline capable of solving problems in molecular biology. We outline the challenges and future prospects for optical single-molecule techniques which can be used in combination with smart labeling strategies to yield quantitative three-dimensional information about the dynamic organization of living cells. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:2642 / 2671
页数:30
相关论文
共 356 条
[71]   Immunofluorescence stimulated emission depletion microscopy [J].
Dyba, M ;
Jakobs, S ;
Hell, SW .
NATURE BIOTECHNOLOGY, 2003, 21 (11) :1303-1304
[72]   The fluctuating enzyme:: a single molecule approach [J].
Edman, L ;
Földes-Papp, Z ;
Wennmalm, S ;
Rigler, R .
CHEMICAL PHYSICS, 1999, 247 (01) :11-22
[73]   Memory landscapes of single-enzyme molecules [J].
Edman, L ;
Rigler, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8266-8271
[74]   Data registration and selective single-molecule analysis using multi-parameter fluorescence detection [J].
Eggeling, C ;
Berger, S ;
Brand, L ;
Fries, JR ;
Schaffer, J ;
Volkmer, A ;
Seidel, CAM .
JOURNAL OF BIOTECHNOLOGY, 2001, 86 (03) :163-180
[75]   Monitoring conformational dynamics of a single molecule by selective fluorescence spectroscopy [J].
Eggeling, C ;
Fries, JR ;
Brand, L ;
Günther, R ;
Seidel, CAM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1556-1561
[76]   Fast 100-nm resolution three-dimensional microscope reveals structural plasticity of mitochondria in live yeast [J].
Egner, A ;
Jakobs, S ;
Hell, SW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3370-3375
[77]   SORTING SINGLE MOLECULES - APPLICATION TO DIAGNOSTICS AND EVOLUTIONARY BIOTECHNOLOGY [J].
EIGEN, M ;
RIGLER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) :5740-5747
[78]   Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy [J].
Enderle, T ;
Ha, T ;
Ogletree, DF ;
Chemla, DS ;
Magowan, C ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :520-525
[79]   Near-field fluorescence microscopy of cells [J].
Enderle, T ;
Ha, T ;
Chemla, DS ;
Weiss, S .
ULTRAMICROSCOPY, 1998, 71 (1-4) :303-309
[80]   A maximum likelihood estimator to distinguish single molecules by their fluorescence decays [J].
Enderlein, J ;
Goodwin, PM ;
VanOrden, A ;
Ambrose, WP ;
Erdmann, R ;
Keller, RA .
CHEMICAL PHYSICS LETTERS, 1997, 270 (5-6) :464-470