TY - JOUR
T1 - Zooming in on biological processes with fluorescence nanoscopy
AU - Agrawal, Utsav
AU - Reilly, Daniel T.
AU - Schroeder, Charles M.
N1 - Funding Information:
This work was supported by a Packard Fellowship from the David and Lucile Packard Foundation (to CMS) and an NIH Molecular Biophysics Training Grant (to DR).
PY - 2013/8
Y1 - 2013/8
N2 - Fluorescence nanoscopy enables the study of biological phenomena at nanometer scale spatial resolution. Recent biological studies using fluorescence nanoscopy have showcased the ability of these techniques to directly observe protein organization, subcellular molecular interactions, structural dynamics, electrical signaling, and diffusion of cytosolic proteins at unprecedented spatial resolution. Super-resolution imaging techniques critically rely on bright fluorescent probes such as organic dyes or fluorescent proteins. Recently, these methods have been extended to live cells and multicolor, three-dimensional imaging, thereby providing exquisite spatiotemporal resolutions of the order of 10-20. nm and 1-2. s for subcellular imaging. Further improvements in image processing algorithms, labeling techniques, correlative microscopy, and development of advanced fluorescent probes will be required to achieve true molecular-scale resolution using these techniques.
AB - Fluorescence nanoscopy enables the study of biological phenomena at nanometer scale spatial resolution. Recent biological studies using fluorescence nanoscopy have showcased the ability of these techniques to directly observe protein organization, subcellular molecular interactions, structural dynamics, electrical signaling, and diffusion of cytosolic proteins at unprecedented spatial resolution. Super-resolution imaging techniques critically rely on bright fluorescent probes such as organic dyes or fluorescent proteins. Recently, these methods have been extended to live cells and multicolor, three-dimensional imaging, thereby providing exquisite spatiotemporal resolutions of the order of 10-20. nm and 1-2. s for subcellular imaging. Further improvements in image processing algorithms, labeling techniques, correlative microscopy, and development of advanced fluorescent probes will be required to achieve true molecular-scale resolution using these techniques.
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U2 - 10.1016/j.copbio.2013.02.016
DO - 10.1016/j.copbio.2013.02.016
M3 - Review article
C2 - 23498844
AN - SCOPUS:84880943233
SN - 0958-1669
VL - 24
SP - 646
EP - 653
JO - Current Opinion in Biotechnology
JF - Current Opinion in Biotechnology
IS - 4
ER -