Literature DB >> 2994768

Model-independent electron spin resonance for measuring order of immobile components in a biological assembly.

T P Burghardt, N L Thompson.   

Abstract

A model-independent description of the angular orientation distribution of elements in an ordered biological assembly is applied to the electron spin resonance (ESR) technique. As in a previous model-independent treatment of fluorescence polarization (Burghardt, T.P., 1984, Biopolymers, 23:2383-2406) the elemental order is described by an angular distribution of molecular frames with one frame fixed in each element of the assembly. The distribution is expanded in a complete orthonormal set of functions. The coefficients of the series expansion (the order parameters) describe the orientation distribution of the elements in the assembly without reference to a model and can be obtained from the observed spectrum. The method establishes the limitations of ESR in detecting order in the assembly by determining which distribution coefficients the technique can detect. A method of determining the order parameters from an ESR spectra, using a set of ESR basis spectra, is developed. We also describe a treatment that incorporates the actual line shape measured from randomly oriented, immobile elements. In this treatment, no model-dependent assumptions about the line shape are required. We have applied the model-independent analysis to ESR spectra from spin-labeled myosin cross-bridges in muscle fibers. The results contain detailed information on the spin-probe angular distribution and differ in interesting ways from previous model-dependent interpretations of the spectra.

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Year:  1985        PMID: 2994768      PMCID: PMC1329354          DOI: 10.1016/S0006-3495(85)83796-6

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


  11 in total

1.  All myosin heads form bonds with actin in rigor rabbit skeletal muscle.

Authors:  R Cooke; K Franks
Journal:  Biochemistry       Date:  1980-05-13       Impact factor: 3.162

2.  A comparison of order and orientation of crossbridges in rigor and relaxed muscle fibres using fluorescence polarization.

Authors:  M G Wilson; R A Mendelson
Journal:  J Muscle Res Cell Motil       Date:  1983-12       Impact factor: 2.698

3.  Order in supported phospholipid monolayers detected by the dichroism of fluorescence excited with polarized evanescent illumination.

Authors:  N L Thompson; H M McConnell; T P Burhardt
Journal:  Biophys J       Date:  1984-12       Impact factor: 4.033

4.  Submillisecond rotational dynamics of spin-labeled myosin heads in myofibrils.

Authors:  D D Thomas; S Ishiwata; J C Seidel; J Gergely
Journal:  Biophys J       Date:  1980-12       Impact factor: 4.033

5.  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

6.  Orientation of spin labels attached to cross-bridges in contracting muscle fibres.

Authors:  R Cooke; M S Crowder; D D Thomas
Journal:  Nature       Date:  1982-12-23       Impact factor: 49.962

7.  Cross-bridge orientation in skeletal muscle measured by linear dichroism of an extrinsic chromophore.

Authors:  J Borejdo; O Assulin; T Ando; S Putnam
Journal:  J Mol Biol       Date:  1982-07-05       Impact factor: 5.469

8.  Calculation of the polarized fluorescence from a labeled muscle fiber.

Authors:  M F Morales
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

9.  Three-dimensional disorder of dipolar probes in a helical array. Application to muscle cross-bridges.

Authors:  R A Mendelson; M G Wilson
Journal:  Biophys J       Date:  1982-08       Impact factor: 4.033

10.  Evidence for cross-bridge order in contraction of glycerinated skeletal muscle.

Authors:  T P Burghardt; T Ando; J Borejdo
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

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  3 in total

1.  Reconstruction of the probe angular distribution from a series of electron spin resonance spectra of tilted oriented samples.

Authors:  T P Burghardt; A R French
Journal:  Biophys J       Date:  1989-09       Impact factor: 4.033

2.  Time-resolved fluorescence polarization from ordered biological assemblies.

Authors:  T P Burghardt
Journal:  Biophys J       Date:  1985-10       Impact factor: 4.033

3.  Myosin cross-bridge orientation in rigor and in the presence of nucleotide studied by electron spin resonance.

Authors:  K Ajtai; A R French; T P Burghardt
Journal:  Biophys J       Date:  1989-09       Impact factor: 4.033

  3 in total

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