Literature DB >> 24226912

Myosin head rotation in muscle fibers measured using polarized fluorescence photobleaching recovery.

E H Hellen1, K Ajtai, T P Burghardt.   

Abstract

The technique of polarized fluorescence photobleaching recovery (PFPR) has been applied for the first time to investigation of the rotational correlation time of the myosin head in muscle fibers. This is a novel application of PFPR because it is the first time PFPR has been applied to a sample which is not cylindrically symmetric about the optical axis. Therefore we present a method for analysis of PFPR results from an oriented sample such as the muscle fibers aligned perpendicularly to the optical axis used here. Control experiments performed on fluorescently labeled myosin heads in solution demonstrate that, under some conditions, our PFPR apparatus can easily measure a rotational correlation time of less than 200 μs. Validity of this application of PFPR to muscle fibers is provided by the agreement of our results with published results from a variety of other spectroscopic techniques. In particular, using glycerinated rabbit psoas muscle fibers, we find that for relaxed fibers and isometrically contracting fibers, the myosin heads undergo high-amplitude rotations on the submillisecond time domain. For fibers in rigor the myosin heads are highly oriented and nearly immobile. For fibers in ADP the myosin heads are highly ordered in a distribution quite different from that in rigor, and they are slightly more mobile than in rigor.

Entities:  

Year:  1995        PMID: 24226912     DOI: 10.1007/BF01152562

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  36 in total

1.  Slow rotational mobilities of antibodies and lipids associated with substrate-supported phospholipid monolayers as measured by polarized fluorescence photobleaching recovery.

Authors:  M M Timbs; N L Thompson
Journal:  Biophys J       Date:  1990-08       Impact factor: 4.033

2.  Microsecond rotational motion of spin-labeled myosin heads during isometric muscle contraction. Saturation transfer electron paramagnetic resonance.

Authors:  V A Barnett; D D Thomas
Journal:  Biophys J       Date:  1989-09       Impact factor: 4.033

3.  Segmental flexibility of the S-1 moiety of myosin.

Authors:  R A Mendelson; M F Morales; J Botts
Journal:  Biochemistry       Date:  1973-06-05       Impact factor: 3.162

4.  Separation of translational and rotational contributions in solution studies using fluorescence photobleaching recovery.

Authors:  W A Wegener; R Rigler
Journal:  Biophys J       Date:  1984-12       Impact factor: 4.033

5.  Saturation effects in polarized fluorescence photobleaching recovery and steady state fluorescence polarization.

Authors:  E H Hellen; T P Burghardt
Journal:  Biophys J       Date:  1994-03       Impact factor: 4.033

6.  Orientation of spin-labeled myosin heads in glycerinated muscle fibers.

Authors:  D D Thomas; R Cooke
Journal:  Biophys J       Date:  1980-12       Impact factor: 4.033

7.  Motion of myosin cross-bridges in skeletal muscle fibers studied by time-resolved fluorescence anisotropy decay.

Authors:  T P Burghardt; N L Thompson
Journal:  Biochemistry       Date:  1985-07-02       Impact factor: 3.162

8.  Protein rotational motion in solution measured by polarized fluorescence depletion.

Authors:  T M Yoshida; B G Barisas
Journal:  Biophys J       Date:  1986-07       Impact factor: 4.033

9.  Probe studies of the MgADP state of muscle cross-bridges: microscopic and wavelength-dependent fluorescence polarization from 1,5-IAEDANS-labeled myosin subfragment 1 decorating muscle fibers.

Authors:  K Ajtai; T P Burghardt
Journal:  Biochemistry       Date:  1987-07-14       Impact factor: 3.162

10.  Stereospecific reaction of muscle fiber proteins with the 5' or 6' isomer of (iodoacetamido)tetramethylrhodamine.

Authors:  K Ajtai; P J Ilich; A Ringler; S S Sedarous; D J Toft; T P Burghardt
Journal:  Biochemistry       Date:  1992-12-15       Impact factor: 3.162

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  1 in total

1.  Probes bound to myosin Cys-707 rotate during length transients in contraction.

Authors:  T P Burghardt; S P Garamszegi; K Ajtai
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

  1 in total

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