MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures

被引:33
作者
Caetano, Fabiana A. [1 ,2 ]
Dirk, Brennan S. [3 ]
Tam, Joshua H. K. [1 ,2 ]
Cavanagh, P. Craig [3 ]
Goiko, Maria [3 ,4 ]
Ferguson, Stephen S. G. [5 ]
Pasternak, Stephen H. [1 ,2 ,6 ]
Dikeakos, Jimmy D. [3 ]
de Bruyn, John R. [4 ]
Heit, Bryan [3 ]
机构
[1] Univ Western Ontario, J Allyn Taylor Ctr Cell Biol, Robarts Res Inst, London, ON, Canada
[2] Univ Western Ontario, Dept Physiol & Pharmacol, London, ON, Canada
[3] Univ Western Ontario, Dept Microbiol & Immunol, London, ON, Canada
[4] Univ Western Ontario, Dept Phys & Astron, London, ON, Canada
[5] Univ Ottawa, Cellular & Mol Med, Ottawa, ON, Canada
[6] Univ Western Ontario, Dept Clin Neurol Sci, Schulich Sch Med, London, ON, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
AMYLOID PRECURSOR PROTEIN; SIGNAL-TRANSDUCTION; DOWN-REGULATION; K-FUNCTION; MEMBRANE; MICROSCOPY; TRAFFICKING; PACS-2; FRET; COLOCALIZATION;
D O I
10.1371/journal.pcbi.1004634
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Our current understanding of the molecular mechanisms which regulate cellular processes such as vesicular trafficking has been enabled by conventional biochemical and microscopy techniques. However, these methods often obscure the heterogeneity of the cellular environment, thus precluding a quantitative assessment of the molecular interactions regulating these processes. Herein, we present Molecular Interactions in Super Resolution (MIiSR) software which provides quantitative analysis tools for use with super-resolution images. MIiSR combines multiple tools for analyzing intermolecular interactions, molecular clustering and image segmentation. These tools enable quantification, in the native environment of the cell, of molecular interactions and the formation of higher-order molecular complexes. The capabilities and limitations of these analytical tools are demonstrated using both modeled data and examples derived from the vesicular trafficking system, thereby providing an established and validated experimental workflow capable of quantitatively assessing molecular interactions and molecular complex formation within the heterogeneous environment of the cell.
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页数:30
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