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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Muscle contraction. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (226 pages)
    Edition: 1st ed.
    ISBN: 9781483275567
    Language: English
    Note: Front Cover -- Muscle and Nonmuscle Motility -- Copyright Page -- Table of Contents -- Contributors -- Preface -- Contents of Volume 1 -- Chapter 1. Preparation and Properties of Dynein ATPase -- I. Introduction -- II. Preparation and Properties of Dynein Isoenzymes from Sea Urchin Sperm Flagella -- III. Preparation and Properties of Dynein ATPases from Other Sources -- IV. Function of Dynein ATPases -- Acknowledgment -- References -- Chapter 2. The Cytoskeleton of the Red Blood Cell -- I. Introduction -- II. Properties of the Red Cell -- III. Nature of the Red Cell Cytoskeleton -- IV. Construction of the Cytoskeleton: Interactions between Constituent Proteins -- V. Interactions of Cytoskeletal Constituents with Other Membrane Components -- VI. Participation of the Cytoskeleton in Cellular Phenomena -- VII. Cytoskeletal Proteins and Cell Maturation -- VIII. The Cytoskeleton in Disease States -- IX. Conservation of Cytoskeletal Proteins: Species Variations -- X. Relation of the Red Cell Cytoskeletonand Its Proteins to Those of Other Eukaryotic Cells -- Acknowledgments -- References -- Chapter 3. Clathrin: A Study of Its Properties and Mechanochemical Role in Cell Functions -- I. Introduction -- II. Properties of Clathrin -- III. General Considerations -- IV. Concluding Remarks -- Acknowledgments -- References -- Chapter 4. New Concepts of the Control of Cell Surface Structure and Function -- I. Introduction -- II. The Control of Membrane Topography -- III. The Role of Tubulin in Membrane Regulation -- IV. Summary -- References -- Index.
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Muscle contraction. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (387 pages)
    Edition: 1st ed.
    ISBN: 9781483264646
    Language: English
    Note: Front Cover -- Muscle and Nonmuscle Motility -- Copyright Page -- Table of Contents -- Contributors -- Preface -- Contents of Volume 2 -- Chapter 1. Molecular Basis of Contraction in Cross-Striated Muscles and Relevance to Motile Mechanisms in Other Cells -- I. Introduction -- II. Structure of Muscle Fibers -- III. Protein Components of the Filaments -- IV. Changes in the Band Pattern of Muscle during Contraction and Stretch -- V. Molecular Structure of the Filaments -- VI. Molecular Changes during Contraction and in Rigor -- VII. Some Biochemical and Physiological Implications of the Structural Results -- VIII. Structural Details of the Cross-Bridge Mechanism -- IX. Outstanding Problems and Future Work -- References -- Chapter 2. Macromolecular Assembly of Myosin -- I. Introduction -- II. Assembly of Myosin Filaments -- III. Assembly of Copolymers of Different Myosins (Hybridization) -- References -- Chapter 3. Macromolecular Assembly of Actin -- I. Introduction -- II. G-F Transformation of Actin -- III. Structure of F-Actin -- IV. Conformation and Interaction of Actin Monomer -- V. Interaction of F-Actin with Regulatory Proteins and Myosin -- VI. Actin and Motility -- VII. Concluding Remarks -- References -- Chapter 4. Regulation of Contractility -- I. Introduction -- II. One Aspect of the Troponin Mechanism: The Role of Troponin T -- III. General Aspects of the Regulatory Mechanism in Vertebrate Smooth Muscle -- IV. Characteristics of Aorta Leiotonin -- V. Troponin in Ascidian Smooth Muscle -- VI. A Regulatory Factor in Slime Mold -- VII. Concluding Remarks -- References -- Chapter 5. The Regulation of Cytoplasmic Ca2+ Concentration in Muscle and Nonmuscle Cells -- I. Introduction -- II. The Sarcoplasmic Reticulum of Skeletal Muscle -- III. The Transport of Ca2+ by Cardiac Sarcoplasmic Reticulum. , IV. The Ca2+ Transport Activities of Cardiac Sarcolemma -- V. Smooth Muscle -- VI. The Regulation of Cytoplasmic Ca2+ Concentration in Nonmuscle Cells -- References -- Index.
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 10 (1971), S. 1316-1321 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 26 (1987), S. 4454-4460 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 467 (1986), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 79 (1957), S. 3729-3737 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 81 (1959), S. 696-700 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 463 (1986), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 435 (1984), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 2 (1982), S. 317-332 
    ISSN: 0886-1544
    Keywords: cytoskeleton ; platelets ; actin-binding protein ; actin ; myosin ; thrombin activation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: When human blood platelets were immersed in an ice-cold solution containing 1% Triton ×-1200, 40 mM KCl, 10 mM EGTA, 10 mM imidazole-HCl, and 2 mM NaN3 pH 7.0, a flocculent precipitate appeared immediately in the tube. This precipitate was collected at 3,000g and SDS-polyacrylamide gel analysis showed it to consist mainly of actin, α-actinin, actin-binding protein (ABP), and varying amounts of myosin.Any modifications of this solution used to isolate the platelets' Triton-insoluble cytoskeleton caused profound changes in the nature of the cytoskeleton isolated. Increasing the KCl concentration resulted in a lower yield of cytoskeletal actin and ABP. Inclusion of EDTA in the solution resulted in an increased amount of myosin associated with the cytoskeleton, whereas including MgATP decreased the myosin yield.Experiments with the purified proteins showed that ABP and myosin can each protect the actin from depolymerizing when dialyzed into the Triton solubilization solution. In addition, it was found that when platelets were stimulated with thrombin for 2 min prior to the addition of the Triton solution, 3-4 times more myosin was associated with the cytoskeletal precipitate.The results suggest, therefore, that any variations in solution conditions used for isolating the cytoskeleton from resting platelets, which results in alterations in the amount of ABP, may have profound effects on the state of actin polymerization. Likewise, in thrombin-activated platelets, it is suggested that the increased association of myosin with the cytoskeleton results in a greater stabilization of the F-actin associated with the cytoskeleton. These factors must be considered when interpreting the results regarding the nature of actin transformations in the resting and activated platelet.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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