PALM and STORM: Into large fields and high-throughput microscopy with sCMOS detectors

被引:34
作者
Almada, Pedro
Culley, Sian
Henriques, Ricardo [1 ]
机构
[1] UCL, Quantitat Imaging & NanoBiophys Grp, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
Single-molecule localization; Hardware; sCMOS; Homogenization; REFLECTION FLUORESCENCE MICROSCOPY; OPTICAL RECONSTRUCTION MICROSCOPY; SUPERRESOLUTION MICROSCOPY; DIFFRACTION-LIMIT; RESOLUTION LIMIT; LOCALIZATION; ILLUMINATION; NANOSCOPY; FLUOROPHORES; TRACKING;
D O I
10.1016/j.ymeth.2015.06.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single Molecule Localization Microscopy (SMLM) techniques such as Photo-Activation Localization Microscopy (PALM) and Stochastic Optical Reconstruction Microscopy (STORM) enable fluorescence microscopy super-resolution: the overcoming of the resolution barrier imposed by the diffraction of light. These techniques are based on acquiring hundreds or thousands of images of single molecules, locating them and reconstructing a higher-resolution image from the high-precision localizations. These methods generally imply a considerable trade-off between imaging speed and resolution, limiting their applicability to high-throughput workflows. Recent advancements in scientific Complementary Metal-Oxide Semiconductor (sCMOS) camera sensors and localization algorithms reduce the temporal requirements for SMLM, pushing it toward high-throughput microscopy. Here we outline the decisions researchers face when considering how to adapt hardware on a new system for sCMOS sensors with high-throughput in mind. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:109 / 121
页数:13
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