Literature DB >> 15695095

FRAP analysis of binding: proper and fitting.

Brian L Sprague1, James G McNally.   

Abstract

Dynamic molecular interactions are fundamental to all cellular processes. In vivo analyses of these interactions are frequently done using fluorescence recovery after photobleaching (FRAP). Proper interpretation of FRAP data yields information about the binding interactions of fluorescently tagged molecules, including the number of binding states and the binding strength of each state. This binding information can be gleaned from appropriate models of the process underlying a FRAP recovery. Continued application and development of these approaches promise to provide crucial information for a quantitative description of the molecular networks that regulate cellular function.

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Year:  2005        PMID: 15695095     DOI: 10.1016/j.tcb.2004.12.001

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  198 in total

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5.  Cross-validating FRAP and FCS to quantify the impact of photobleaching on in vivo binding estimates.

Authors:  Timothy J Stasevich; Florian Mueller; Ariel Michelman-Ribeiro; Tilman Rosales; Jay R Knutson; James G McNally
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

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Journal:  Chromosome Res       Date:  2011-01       Impact factor: 5.239

8.  FRAP analysis of membrane-associated proteins: lateral diffusion and membrane-cytoplasmic exchange.

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Journal:  Biophys J       Date:  2010-10-20       Impact factor: 4.033

Review 9.  Src/FAK-mediated regulation of E-cadherin as a mechanism for controlling collective cell movement: insights from in vivo imaging.

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10.  Single-Molecule Tracking and Its Application in Biomolecular Binding Detection.

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Journal:  IEEE J Sel Top Quantum Electron       Date:  2016-05-17       Impact factor: 4.544

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