Literature DB >> 17513376

GFP-tagged regulatory light chain monitors single myosin lever-arm orientation in a muscle fiber.

Thomas P Burghardt1, Katalin Ajtai, Daniel K Chan, Miriam F Halstead, Jinhui Li, Ye Zheng.   

Abstract

Myosin is the molecular motor in muscle-binding actin and executing a power stroke by rotating its lever arm through an angle of approximately 70 degrees to translate actin against resistive force. A green fluorescent protein (GFP)-tagged human cardiac myosin regulatory light chain (HCRLC) was constructed to study in situ lever arm orientation one molecule at a time by polarized fluorescence emitted from the GFP probe. The recombinant protein physically and functionally replaced the native RLC on myosin lever arms in the thick filaments of permeabilized skeletal muscle fibers. Detecting single molecules in fibers where myosin concentration reaches 300 microM is accomplished using total internal reflection fluorescence microscopy. With total internal reflection fluorescence, evanescent field excitation, supercritical angle fluorescence detection, and CCD detector pixel size limits detection volume to just a few attoliters. Data analysis manages both the perturbing effect of the TIR interface on probe emission and the effect of high numerical aperture collection of light. The natural myosin concentration gradient in a muscle fiber allows observation of fluorescence polarization from C-term GFP-tagged HCRLC exchanged myosin from regions in the thick filament containing low and high myosin concentrations. In rigor, cross-bridges at low concentration at the end of the thick filament maintain GFP dipole moments at two distinct polar angles relative to the fiber symmetry axis. The lower angle, where the dipole is nearly parallel to fiber axis, is more highly populated than the alternative, larger angle. Cross-bridges at higher concentration in the center of the thick filament are oriented in a homogeneous band at approximately 45 degrees to the fiber axis. The data suggests molecular crowding impacts myosin conformation, implying mutual interactions between cross-bridges alter how the muscle generates force. The GFP-tagged RLC is a novel probe to assess single-lever-arm orientation characteristics in situ.

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Year:  2007        PMID: 17513376      PMCID: PMC1959555          DOI: 10.1529/biophysj.107.107433

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  63 in total

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  17 in total

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Authors:  Thomas P Burghardt; Laura A Sikkink
Journal:  Biochemistry       Date:  2013-02-06       Impact factor: 3.162

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10.  Single myosin lever arm orientation in a muscle fiber detected with photoactivatable GFP.

Authors:  Thomas P Burghardt; Jinhui Li; Katalin Ajtai
Journal:  Biochemistry       Date:  2009-02-03       Impact factor: 3.162

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