Literature DB >> 8396449

Saturation transfer electron parametric resonance of an indane-dione spin-label. Calibration with hemoglobin and application to myosin rotational dynamics.

O Roopnarine1, K Hideg, D D Thomas.   

Abstract

We have used a recently synthesized indane-dione spin label (2-[-oxyl-2,2,5,5-tetramethyl-3-pyrrolin-3-yl)methenyl]in dane-1,3-dione (InVSL) to study the rotational dynamics of myosin, with saturation-transfer electron paramagnetic resonance (ST-EPR). To determine effective rotational correlation times (tau effr) from InVSL spectra, reference spectra corresponding to known correlation times (tau r) were obtained from InVSL-hemoglobin undergoing isotropic rotational motion in aqueous glycerol solutions. These spectra were used to generate plots of spectral parameters vs. tau r. These plots should be used to analyze ST-EPR spectra of InVSL bound to other proteins, because the spectra are different from those of tempo-maleimide-spin-labeled hemoglobin, which have been used previously as ST-EPR standards. InVSL was covalently attached to the head (subfragment-1; S1) of myosin. EPR spectra and K/EDTA-ATPase activity showed that 70-95% of the heads were labeled, with > or = 90% of the label bound to either cys 707 (SH1) or cys 697 (SH2). ST-EPR spectra of InVSL-S1 attached to glass beads, bound to actin in myofibrils, or precipitated with ammonium sulfate indicated no submillisecond rotational motion. Therefore, InVSL is rigidly immobilized on the protein so that it reports the global rotation of the myosin head. The ST-EPR spectra of InVSL-myosin monomers and filaments indicated tau effr values of 4 and 13 microseconds, respectively, showing that myosin heads undergo microsecond segmental rotations that are more restricted in filaments than in monomers. The observed tau effr values are longer than those previously obtained with other spin labels bound to myosin heads, probably because InVSL binds more rigidly to the protein and/or with a different orientation. Further EPR studies of InVSL-myosin in solution and in muscle fibers should prove complementary to previous work with other labels.

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Year:  1993        PMID: 8396449      PMCID: PMC1262524          DOI: 10.1016/S0006-3495(93)81561-3

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


  31 in total

1.  Motion of subfragment-1 in myosin and its supramolecular complexes: saturation transfer electron paramagnetic resonance.

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Journal:  Proc Natl Acad Sci U S A       Date:  1975-05       Impact factor: 11.205

2.  Rotational dynamics of actin-bound intermediates in the myosin ATPase cycle.

Authors:  C L Berger; D D Thomas
Journal:  Biochemistry       Date:  1991-11-19       Impact factor: 3.162

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Journal:  Biochemistry       Date:  1970-08-04       Impact factor: 3.162

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Journal:  J Biochem       Date:  1966-01       Impact factor: 3.387

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Authors:  S Ohnishi; J C Boeyens; H M McConnell
Journal:  Proc Natl Acad Sci U S A       Date:  1966-09       Impact factor: 11.205

7.  Simulation of saturation transfer electron paramagnetic resonance spectra for rotational motion with restricted angular amplitude.

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Journal:  Biophys J       Date:  1993-03       Impact factor: 4.033

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Journal:  J Mol Biol       Date:  1984-10-15       Impact factor: 5.469

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Authors:  S S Margossian; S Lowey
Journal:  Methods Enzymol       Date:  1982       Impact factor: 1.600

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

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  8 in total

1.  Independent mobility of catalytic and regulatory domains of myosin heads.

Authors:  B Adhikari; K Hideg; P G Fajer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

Review 2.  Use of electron paramagnetic resonance spectroscopy to evaluate the redox state in vivo.

Authors:  Harold M Swartz; Nadeem Khan; Valery V Khramtsov
Journal:  Antioxid Redox Signal       Date:  2007-10       Impact factor: 8.401

3.  Orientation of intermediate nucleotide states of indane dione spin-labeled myosin heads in muscle fibers.

Authors:  O Roopnarine; D D Thomas
Journal:  Biophys J       Date:  1996-06       Impact factor: 4.033

4.  Graphical evaluation of alkylation of myosin's SH1 and SH2: the N-phenylmaleimide reaction.

Authors:  L Xie; W X Li; V A Barnett; M Schoenberg
Journal:  Biophys J       Date:  1997-02       Impact factor: 4.033

5.  Synthesis of a spin-labeled photoaffinity ATP analogue, and its use to specifically photolabel myosin cross-bridges in skeletal muscle fibers.

Authors:  D Wang; Y Luo; R Cooke; J Grammer; E Pate; R G Yount
Journal:  J Muscle Res Cell Motil       Date:  1999-11       Impact factor: 2.698

6.  Resolution of three structural states of spin-labeled myosin in contracting muscle.

Authors:  E M Ostap; V A Barnett; D D Thomas
Journal:  Biophys J       Date:  1995-07       Impact factor: 4.033

7.  A spin label that binds to myosin heads in muscle fibers with its principal axis parallel to the fiber axis.

Authors:  O Roopnarine; D D Thomas
Journal:  Biophys J       Date:  1994-10       Impact factor: 4.033

8.  Orientational dynamics of indane dione spin-labeled myosin heads in relaxed and contracting skeletal muscle fibers.

Authors:  O Roopnarine; D D Thomas
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

  8 in total

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