期刊
NATURE PROTOCOLS
卷 10, 期 12, 页码 1948-1974出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2015.100
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资金
- NUS-BW (National University of Singapore/Baden-Wurttemberg BW)
- Heidelberg Graduate School of Mathematical and Computational Methods for the Sciences
- National University of Singapore
- Singapore National Research Foundation
- Singapore Ministry of Education [MOE2012-T3-1-008]
Single-plane illumination (SPIM) or total internal reflection fluorescence (TIRF) microscopes can be combined with fast and single-molecule-sensitive cameras to allow spatially resolved fluorescence (cross-) correlation spectroscopy (FCS or FCCS, hereafter referred to FCS/FCCS). This creates a powerful quantitative bioimaging tool that can generate spatially resolved mobility and interaction maps with hundreds to thousands of pixels per sample. These massively parallel imaging schemes also cause less photodamage than conventional single-point confocal microscopy-based FCS/FCCS. Here we provide guidelines for imaging FCS/FCCS measurements on commercial and custom-built microscopes (including sample preparation, setup calibration, data acquisition and evaluation), as well as anticipated results for a variety of in vitro and in vivo samples. For a skilled user of an available SPIM or TIRF setup, sample preparation, microscope alignment, data acquisition and data fitting, as described in this protocol, will take similar to 1 d, depending on the sample and the mode of imaging.
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