Literature DB >> 3013331

Applications of new saturation transfer electron paramagnetic resonance methodology to the rotational dynamics of the Ca-ATPase in sarcoplasmic reticulum membranes.

T C Squier, D D Thomas.   

Abstract

The presence of small amounts of weakly immobilized probes can result in large systematic errors in the measurement of correlation times (tau r) from saturation transfer EPR spectra. However, we have recently developed experimental methodology to minimize these errors (Squier and Thomas, Biophys. J., 49:921-935). In the present study we have applied this methodology to the measurement of the rotational motion of the Ca-ATPase in sarcoplasmic reticulum. This analysis involves the estimate of tau r from line-shape parameters (spectral line-height ratios) and intensity parameters (spectral integral), coupled with digital subtractions to remove spectral components corresponding to weakly immobilized probes. We have analyzed the ST-EPR spectra of the Ca-ATPase over a range of temperatures and find that, unlike line-shape parameters, intensity parameters are little affected by the subtraction of the weakly immobilized spectral component (W). Thus, tau r values from intensity parameters are a more reliable measurement of rotational motion. As reported previously, an analysis with line-shape parameters yields a nonlinear Arrhenius plot of protein mobility. However, the plot is linear when intensity parameters or corrected spectra are used, consistent with the theory for the hydrodynamic properties of a membrane protein of unchanging size and shape in a fluid bilayer. An analysis with line-shape parameters yields different effective tau r values in different spectral regions, and these tau r values are temperature-dependent. However, correction of spectra for W yields temperature-independent tau r ratios, indicating that the motional anisotropy is temperature-independent. Obtaining a good match for the weakly immobilized spectral component remains a major difficulty in the quantitative analysis of ST-EPR spectra using line-shape parameters. This study shows that intensity parameters can be used to avoid this problem, making the ST-EPR technique applicable in cases that were previously resistant to analysis.

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Year:  1986        PMID: 3013331      PMCID: PMC1329544          DOI: 10.1016/S0006-3495(86)83721-3

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


  16 in total

1.  Rotational motion and evidence for oligomeric structures of sarcoplasmic reticulum Ca2+-activated ATPase.

Authors:  W Hoffmann; M G Sarzala; D Chapman
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

2.  Rotational motion of the sarcoplasmic reticulum Ca2+-ATPase.

Authors:  D D Thomas; C Hidalgo
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

3.  Saturation transfer electron spin resonance study on the rotational diffusion of calcium- and magnesium-dependent adenosine triphosphatase in sarcoplasmic reticulum membranes.

Authors:  Y Kirino; T Ohkuma; H Shimizu
Journal:  J Biochem       Date:  1978-07       Impact factor: 3.387

4.  Methodology for increased precision in saturation transfer electron paramagnetic resonance studies of rotational dynamics.

Authors:  T C Squier; D D Thomas
Journal:  Biophys J       Date:  1986-04       Impact factor: 4.033

5.  Effect of the lipid environment on protein motion and enzymatic activity of sarcoplasmic reticulum calcium ATPase.

Authors:  C Hidalgo; D D Thomas; N Ikemoto
Journal:  J Biol Chem       Date:  1978-10-10       Impact factor: 5.157

6.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

7.  Highly purified sarcoplasmic reticulum vesicles are devoid of Ca2+-independent ('basal') ATPase activity.

Authors:  J L Fernandez; M Rosemblatt; C Hidalgo
Journal:  Biochim Biophys Acta       Date:  1980-07

8.  Molecular motion in phospholipid bilayers in the gel phase: long axis rotation.

Authors:  D Marsh
Journal:  Biochemistry       Date:  1980-04-15       Impact factor: 3.162

9.  A saturation transfer electron spin resonance study on the break in the Arrhenius plot for the rotational motion of Ca2+-dependent adenosine triphosphatase molecules in purified and lipid-replaced preparations of rabbit skeletal muscle sarcoplasmic reticulum.

Authors:  T Kaizu; Y Kirino; H Shimizu
Journal:  J Biochem       Date:  1980-12       Impact factor: 3.387

10.  The effects of deoxycholate and trypsin on the cross-linking of rabbit skeletal muscle sarcoplasmic reticulum proteins.

Authors:  C F Louis; J A Holroyd
Journal:  Biochim Biophys Acta       Date:  1978-08-21
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  4 in total

1.  Methodology for increased precision in saturation transfer electron paramagnetic resonance studies of rotational dynamics.

Authors:  T C Squier; D D Thomas
Journal:  Biophys J       Date:  1986-04       Impact factor: 4.033

2.  Saturation transfer electron spin resonance of Ca2(+)-ATPase covalently spin-labeled with beta-substituted vinyl ketone- and maleimide-nitroxide derivatives. Effects of segmental motion and labeling levels.

Authors:  L I Horváth; L Dux; H O Hankovszky; K Hideg; D Marsh
Journal:  Biophys J       Date:  1990-07       Impact factor: 4.033

3.  Selective detection of the rotational dynamics of the protein-associated lipid hydrocarbon chains in sarcoplasmic reticulum membranes.

Authors:  T C Squier; D D Thomas
Journal:  Biophys J       Date:  1989-10       Impact factor: 4.033

4.  HNO enhances SERCA2a activity and cardiomyocyte function by promoting redox-dependent phospholamban oligomerization.

Authors:  Vidhya Sivakumaran; Brian A Stanley; Carlo G Tocchetti; Jeff D Ballin; Viviane Caceres; Lufang Zhou; Gizem Keceli; Peter P Rainer; Dong I Lee; Sabine Huke; Mark T Ziolo; Evangelia G Kranias; John P Toscano; Gerald M Wilson; Brian O'Rourke; David A Kass; James E Mahaney; Nazareno Paolocci
Journal:  Antioxid Redox Signal       Date:  2013-10-10       Impact factor: 8.401

  4 in total

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