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Dynamics of fluorescence polarization in macromolecules.
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Spectroscopic study of conformational changes in subdomain 1 of G-actin: influence of divalent cations.
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Synthesis and characterization of two fluorescent sulfhydryl reagents.
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The measurement of actin concentration in solution: a comparison of methods.
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Nanosecond pulsefluorometry in polarized light of G-actin-epsilon-ATP and F-actin-epsilon-ADP.
FEBS Lett. 1975 Mar 15;52(1):8-12
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Nanosecond pulse fluorometry in polarized light of dansyl-L-cysteine linked to a unique SH group of F-actin; the influence of regulatory proteins and myosin moiety.
FEBS Lett. 1975 Dec 1;60(1):164-7
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Fluorescence spectroscopy of proteins.
Science. 1968 Nov 1;162(3853):526-33
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Electron microscopic particle length of F-actin polymerized in vitro.
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The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin.
J Biol Chem. 1971 Aug 10;246(15):4866-71
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Dynamic study of F-actin by quasielastic scattering of laser light.
J Mol Biol. 1971 Nov 28;62(1):251-65
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Fluorescence study of N-(3-pyrene)maleimide conjugated to rabbit skeletal F-actin and plasmodium actin polymers.
Biochim Biophys Acta. 1976 Sep 28;446(1):166-78
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Study of actin and its interactions with heavy meromyosin and the regulatory proteins by the pulse fluorimetry in polarized light of a fluorescent probe attached to an actin cysteine.
Eur J Biochem. 1978 Aug 1;88(2):411-9
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Anisotropy decay of labelled actin. Evidence of the flexibility of the peptide chain in F-actin molecules.
Eur J Biochem. 1979 Jan 15;93(2):397-408
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Rotational dynamics of spin-labeled F-actin in the sub-millisecond time range.
J Mol Biol. 1979 Aug 15;132(3):257-73
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A fluorescent probe for conformational changes in skeletal muscle G-actin.
J Biol Chem. 1980 Oct 10;255(19):8991-3
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Fluorescence anisotropy of labeled F-actin: influence of divalent cations on the interaction between F-actin and myosin heads.
Biochemistry. 1982 Jul 20;21(15):3661-5
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Fluorescence anisotropy of labelled F-actin. Influence of Ca2+ on the flexibility of F-actin.
Biophys Chem. 1982 Oct;16(2):165-72
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Internal motion of F-actin in 10(-6)-10(-3) s time range studied by transient absorption anisotropy: detection of torsional motion.
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Förster-type energy transfer as a probe for changes in local fluctuations of the protein matrix.
Biochemistry. 1984 Jul 17;23(15):3403-11
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Methodology for increased precision in saturation transfer electron paramagnetic resonance studies of rotational dynamics.
Biophys J. 1986 Apr;49(4):921-35
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Evidence that the N-terminal region of A1-light chain of myosin interacts directly with the C-terminal region of actin. A proton magnetic resonance study.
Eur J Biochem. 1987 Apr 1;164(1):259-66
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Spatial relationship between the nucleotide-binding site, Lys-61 and Cys-374 in actin and a conformational change induced by myosin subfragment-1 binding.
Eur J Biochem. 1987 Oct 15;168(2):339-45
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Influence of the bound nucleotide on the molecular dynamics of actin.
Eur J Biochem. 1988 Aug 1;175(2):271-4
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An EPR study of the rotational dynamics of actins from striated and smooth muscle and their complexes with heavy meromyosin.
Eur J Biochem. 1988 Aug 15;175(3):557-64
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Inhibition of sliding movement of F-actin by crosslinking emphasizes the role of actin structure in the mechanism of motility.
J Mol Biol. 1990 Dec 5;216(3):761-72
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The dynamics of actin and myosin association and the crossbridge model of muscle contraction.
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Localization of the tightly bound divalent-cation-dependent and nucleotide-dependent conformation changes in G-actin using limited proteolytic digestion.
Eur J Biochem. 1993 Feb 1;211(3):731-42
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Structure of the actin-myosin complex and its implications for muscle contraction.
Science. 1993 Jul 2;261(5117):58-65
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A conformational change in the actin subunit can change the flexibility of the actin filament.
J Mol Biol. 1993 Jul 20;232(2):334-41
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Structural dynamics of F-actin: I. Changes in the C terminus.
J Mol Biol. 1995 Feb 3;245(5):582-97
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Flexibility of actin filaments derived from thermal fluctuations. Effect of bound nucleotide, phalloidin, and muscle regulatory proteins.
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Structural studies on the ribbon-to-helix transition in profilin: actin crystals.
Biophys J. 1995 Apr;68(4 Suppl):12S-17S; discussion 17S-18S
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Mg- and Ca-actin filaments appear virtually identical in steady-state as determined by dynamic light scattering.
Biochim Biophys Acta. 1995 Dec 6;1253(2):129-32
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Mobility of the N-terminal segment of rabbit skeletal muscle F-actin detected by 1H and 19F nuclear magnetic resonance spectroscopy.
Biochemistry. 1996 Oct 1;35(39):12686-93
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Direct measurement of the torsional rigidity of single actin filaments.
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A correlative analysis of actin filament assembly, structure, and dynamics.
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Complete amino-acid sequence of actin of rabbit skeletal muscle.
Proc Natl Acad Sci U S A. 1973 Sep;70(9):2687-91
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