Literature DB >> 7499476

Fluorescence polarization study of the rigor complexes formed at different degrees of saturation of actin filaments with myosin subfragment-1.

O A Andreev1, R Takashi, J Borejdo.   

Abstract

A serine residue located in the active site of myosin head (S1) was labelled by 9-anthroylnitrile, an amino group located in the central domain of S1 was labelled by 7-diethylamino-3-(4'-isothio-cyanato-phenyl)-4-methylcoumari n, a cysteine residue located near the C-terminus of S1 was labelled by 5-[2-((iodoacetyl)-amino)ethyl]-amino-naphthalene-1-sulfonic acid (1,5-IAEDANS) and a cysteine residue located near the C-terminus of the alkali light chain 1 was labelled with iodoacetamido-tetramethyl-rhodamine. Polarization of fluorescence of S1 was measured in solution (where it indicated the mobility of actin-bound S1) and in myofibrils (where it indicated orientation of probes) to check whether the anisotropy of S1 labelled at different positions depended on the molar ratio S1:actin. In solution, when increasing amounts of actin were added to a fixed amount of labelled S1 (i.e. when myosin heads were initially in excess over actin), anisotropy saturated at 1 mol of S1 per 1 mol of actin. When increasing amounts of S1 were added to a fixed amount of F-actin (i.e. when actin was initially in excess over S1), the anisotropy saturated at 1 mol of S1 per 2 mols of actin. In myofibrils, orientation of S1 was different when S1 was added at nanomolar concentration (intrinsic actin was in excess over extrinsic S1) then when it was added at micromolar concentration (excess of S1 over actin). The fact that the anisotropy of S1 labelled at different positions depended on the molar ratio excluded the possibility that changes were confined to one part of the cross-bridge and supports our earlier proposal that the two rigor complexes which S1 can form with F-actin differ globally in conformation.

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Year:  1995        PMID: 7499476     DOI: 10.1007/bf00114501

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  47 in total

1.  Velocity of movement of actin filaments in in vitro motility assay. Measured by fluorescence correlation spectroscopy.

Authors:  J Borejdo; S Burlacu
Journal:  Biophys J       Date:  1992-05       Impact factor: 4.033

2.  The limited tryptic cleavage of chymotryptic S-1: an approach to the characterization of the actin site in myosin heads.

Authors:  D Mornet; P Pantel; E Audemard; R Kassab
Journal:  Biochem Biophys Res Commun       Date:  1979-08-13       Impact factor: 3.575

3.  The myosin head can bind two actin monomers.

Authors:  O A Andreev; J Borejdo
Journal:  Biochem Biophys Res Commun       Date:  1991-05-31       Impact factor: 3.575

4.  Actin-attached and detached crossbridges in myofibrils: segregation into two populations according to their sensitivity to proteolytic digestion of myosin heavy chain.

Authors:  O Assulin; J Borejdo; C Flynn
Journal:  J Muscle Res Cell Motil       Date:  1986-04       Impact factor: 2.698

5.  Nucleotide-induced change of the interaction between the 20- and 26-kilodalton heavy-chain segments of myosin adenosinetriphosphatase revealed by chemical cross-linking via the reactive thiol SH2.

Authors:  T Hiratsuka
Journal:  Biochemistry       Date:  1987-06-02       Impact factor: 3.162

6.  Studies on the chymotryptic digestion of myosin. Effects of divalent cations on proteolytic susceptibility.

Authors:  A G Weeds; B Pope
Journal:  J Mol Biol       Date:  1977-04       Impact factor: 5.469

7.  Synthesis and characterization of two fluorescent sulfhydryl reagents.

Authors:  E N Hudson; G Weber
Journal:  Biochemistry       Date:  1973-10-09       Impact factor: 3.162

8.  Two different rigor complexes of myosin subfragment 1 and actin.

Authors:  O A Andreev; A L Andreeva; V S Markin; J Borejdo
Journal:  Biochemistry       Date:  1993-11-16       Impact factor: 3.162

9.  Förster energy transfer measurements of thiol 1 to thiol 2 distances in myosin subfragment 1.

Authors:  R E Dalbey; J Weiel; R G Yount
Journal:  Biochemistry       Date:  1983-09-27       Impact factor: 3.162

10.  Three-dimensional structure of myosin subfragment-1: a molecular motor.

Authors:  I Rayment; W R Rypniewski; K Schmidt-Bäse; R Smith; D R Tomchick; M M Benning; D A Winkelmann; G Wesenberg; H M Holden
Journal:  Science       Date:  1993-07-02       Impact factor: 47.728

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  6 in total

1.  Interaction of myosin with F-actin: time-dependent changes at the interface are not slow.

Authors:  J Van Dijk; F Céline; T Barman; P Chaussepied
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

2.  Fluorescence depolarization of actin filaments in reconstructed myofibers: the effect of S1 or pPDM-S1 on movements of distinct areas of actin.

Authors:  Yu S Borovikov; I V Dedova; C G dos Remedios; N N Vikhoreva; P G Vikhorev; S V Avrova; T L Hazlett; B W Van Der Meer
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

3.  Unique charge distribution in surface loops confers high velocity on the fast motor protein Chara myosin.

Authors:  Kohji Ito; Yukie Yamaguchi; Kenji Yanase; Yousuke Ichikawa; Keiichi Yamamoto
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-02       Impact factor: 11.205

4.  Actin motion on microlithographically functionalized myosin surfaces and tracks.

Authors:  D V Nicolau; H Suzuki; S Mashiko; T Taguchi; S Yoshikawa
Journal:  Biophys J       Date:  1999-08       Impact factor: 4.033

5.  Orientation of cross-bridges in skeletal muscle measured with a hydrophobic probe.

Authors:  M Xiao; J Borejdo
Journal:  Biophys J       Date:  1997-05       Impact factor: 4.033

6.  GFP-tagged regulatory light chain monitors single myosin lever-arm orientation in a muscle fiber.

Authors:  Thomas P Burghardt; Katalin Ajtai; Daniel K Chan; Miriam F Halstead; Jinhui Li; Ye Zheng
Journal:  Biophys J       Date:  2007-05-18       Impact factor: 4.033

  6 in total

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