Literature DB >> 28510208

Mesoscopic analysis of motion and conformation of cross-bridges.

J Borejdo1, R Rich2, K Midde2.   

Abstract

The orientation of a cross-bridge is widely used as a parameter in determining the state of muscle. The conventional measurements of orientation, such as that made by wide-field fluorescence microscopy, electron paramagnetic resonance (EPR) or X-ray diffraction or scattering, report the average orientation of 1012-109 myosin cross-bridges. Under conditions where all the cross-bridges are immobile and assume the same orientation, for example in normal skeletal muscle in rigor, it is possible to determine the average orientation from such global measurements. But in actively contracting muscle, where a parameter indicating orientation fluctuates in time, the measurements of the average value provide no information about cross-bridge kinetics. To avoid problems associated with averaging information from trillions of cross-bridges, it is necessary to decrease the number of observed cross-bridges to a mesoscopic value (i.e. the value affected by fluctuations around the average). In such mesoscopic regimes, the averaging of the signal is minimal and dynamic behavior can be examined in great detail. Examples of mesoscopic analysis on skeletal and cardiac muscle are provided.

Entities:  

Keywords:  Fluorescence polarization; Mesoscopic measurements; Myosin cross-bridge orientation

Year:  2012        PMID: 28510208      PMCID: PMC5425693          DOI: 10.1007/s12551-012-0074-y

Source DB:  PubMed          Journal:  Biophys Rev        ISSN: 1867-2450


  86 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-13       Impact factor: 11.205

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Authors:  Thomas P Burghardt; Katalin Ajtai; Julian Borejdo
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Journal:  Biophys J       Date:  2011-09-07       Impact factor: 4.033

5.  Active streaming in human thrombosthenin solutions.

Authors:  I Cohen; R Tirosh; A Oplatka
Journal:  Pflugers Arch       Date:  1974       Impact factor: 3.657

6.  In situ fluorescent protein imaging with metal film-enhanced total internal reflection microscopy.

Authors:  Thomas P Burghardt; Jon E Charlesworth; Miriam F Halstead; James E Tarara; Katalin Ajtai
Journal:  Biophys J       Date:  2006-03-24       Impact factor: 4.033

7.  Orientation of the myosin light chain region by single molecule total internal reflection fluorescence polarization microscopy.

Authors:  Margot E Quinlan; Joseph N Forkey; Yale E Goldman
Journal:  Biophys J       Date:  2005-05-13       Impact factor: 4.033

8.  Nuclear magnetic resonance evidence using D2O for structured water in muscle and brain.

Authors:  F W Cope
Journal:  Biophys J       Date:  1969-03       Impact factor: 4.033

9.  Reconciling the working strokes of a single head of skeletal muscle myosin estimated from laser-trap experiments and crystal structures.

Authors:  John Sleep; Alexandre Lewalle; David Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-20       Impact factor: 11.205

10.  Structural changes accompanying phosphorylation of tarantula muscle myosin filaments.

Authors:  R Craig; R Padrón; J Kendrick-Jones
Journal:  J Cell Biol       Date:  1987-09       Impact factor: 10.539

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  1 in total

1.  Comparison of orientation and rotational motion of skeletal muscle cross-bridges containing phosphorylated and dephosphorylated myosin regulatory light chain.

Authors:  Krishna Midde; Ryan Rich; Peter Marandos; Rafal Fudala; Amy Li; Ignacy Gryczynski; Julian Borejdo
Journal:  J Biol Chem       Date:  2013-01-14       Impact factor: 5.157

  1 in total

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