3D SUPERRESOLUTION MICROSCOPY;
3-DIMENSIONAL LOCALIZATION;
COLOCALIZATION ANALYSIS;
PROTEIN HETEROGENEITY;
FLUORESCENT MOLECULES;
DIFFRACTION-LIMIT;
CLUSTER-ANALYSIS;
RNA-POLYMERASE;
WHOLE-CELL;
REVEALS;
D O I:
10.1016/j.tcb.2020.07.005
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Super-resolution microscopy, and specifically single-molecule localization microscopy (SMLM), is becoming a transformative technology for cell biology, as it allows the study of cellular structures with nanometer resolution. Here, we review a wide range of data analyses approaches for SMLM that extract quantitative information about the distribution, size, shape, spatial organization, and stoichiometry of macromolecular complexes to guide biological interpretation. We present a case study using the nuclear pore complex as an example that highlights the power of combining complementary approaches by identifying its symmetry, ringlike structure, and protein copy number. In face of recent technical and computational advances, this review serves as a guideline for selecting appropriate analysis tools and controls to exploit the potential of SMLM for a wide range of biological questions.
机构:
Univ New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia
Univ New South Wales, Sch Med Sci, EMBL Australia Node Single Mol Sci, Sydney, NSW, AustraliaUniv New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia
Nicovich, Philip R.
Owen, Dylan M.
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机构:
Kings Coll London, Dept Phys & Randall, Div Cell & Mol Biophys, London WC2R 2LS, EnglandUniv New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia
Owen, Dylan M.
Gaus, Katharina
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机构:
Univ New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia
Univ New South Wales, Sch Med Sci, EMBL Australia Node Single Mol Sci, Sydney, NSW, AustraliaUniv New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia