Exploring bacterial cell biology with single-molecule tracking and super-resolution imaging

被引:201
作者
Gahlmann, Andreas [1 ]
Moerner, W. E. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
瑞士国家科学基金会;
关键词
NUCLEOID-ASSOCIATED PROTEIN; ESCHERICHIA-COLI; BACILLUS-SUBTILIS; CAULOBACTER-CRESCENTUS; STRUCTURAL MAINTENANCE; LOCALIZATION MICROSCOPY; FLUORESCENT PROTEINS; ACTIN CYTOSKELETON; RESOLUTION LIMIT; GENE-EXPRESSION;
D O I
10.1038/nrmicro3154
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ability to detect single molecules in live bacterial cells enables us to probe biological events one molecule at a time and thereby gain knowledge of the activities of intracellular molecules that remain obscure in conventional ensemble-averaged measurements. Single-molecule fluorescence tracking and super-resolution imaging are thus providing a new window into bacterial cells and facilitating the elucidation of cellular processes at an unprecedented level of sensitivity, specificity and spatial resolution. In this Review, we consider what these technologies have taught us about the bacterial cytoskeleton, nucleoid organization and the dynamic processes of transcription and translation, and we also highlight the methodological improvements that are needed to address a number of experimental challenges in the field.
引用
收藏
页码:9 / 22
页数:14
相关论文
共 140 条
[51]   Photoswitches: Key molecules for subdiffraction-resolution fluorescence imaging and molecular quantification [J].
Heilemann, Mike ;
Dedecker, Peter ;
Hofkens, Johan ;
Sauer, Markus .
LASER & PHOTONICS REVIEWS, 2009, 3 (1-2) :180-202
[52]  
Hell SW, 2009, NAT METHODS, V6, P24, DOI [10.1038/NMETH.1291, 10.1038/nmeth.1291]
[53]   BREAKING THE DIFFRACTION RESOLUTION LIMIT BY STIMULATED-EMISSION - STIMULATED-EMISSION-DEPLETION FLUORESCENCE MICROSCOPY [J].
HELL, SW ;
WICHMANN, J .
OPTICS LETTERS, 1994, 19 (11) :780-782
[54]   Ultra-high resolution imaging by fluorescence photoactivation localization microscopy [J].
Hess, Samuel T. ;
Girirajan, Thanu P. K. ;
Mason, Michael D. .
BIOPHYSICAL JOURNAL, 2006, 91 (11) :4258-4272
[55]   Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins [J].
Hofmann, M ;
Eggeling, C ;
Jakobs, S ;
Hell, SW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (49) :17565-17569
[56]  
Huang F, 2013, NAT METHODS, V10, P653, DOI [10.1038/nmeth.2488, 10.1038/NMETH.2488]
[57]   FtsZ Ring Stability: of Bundles, Tubules, Crosslinks, and Curves [J].
Huang, Kuo-Hsiang ;
Durand-Heredia, Jorge ;
Janakiraman, Anuradha .
JOURNAL OF BACTERIOLOGY, 2013, 195 (09) :1859-1868
[58]  
Illian Janine, 2008, STAT ANAL MODELLING
[59]   Structure-activity relationship of S-benzylisothiourea derivatives to induce spherical cells in Escherichia coli [J].
Iwai, N ;
Ebata, T ;
Nagura, H ;
Kitazume, T ;
Nagai, K ;
Wachi, M .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2004, 68 (11) :2265-2269
[60]   Super-resolution imaging of the bacterial cytokinetic protein FtsZ [J].
Jennings, Phoebe C. ;
Cox, Guy C. ;
Monahan, Leigh G. ;
Harry, Elizabeth J. .
MICRON, 2011, 42 (04) :336-341