Literature DB >> 6379194

Binding and location of AMP deaminase in rabbit psoas muscle myofibrils.

J Cooper, J Trinick.   

Abstract

It is shown that an interaction exists between AMP deaminase (EC 3.5.4.6) and myofibrils that is sufficiently strong (Kd congruent to 10(-10) M) for more than 99% of the binding sites for the enzyme to be filled in vivo. The binding is not strong enough, however, to stop removal of the enzyme during the extensive washing normally used in the preparation of myofibrils. Fluorescent antibodies to the enzyme label myofibrils close to the junction of the A- and I-bands. The invariance of the position of the antibody stripes at this site, over a range of sarcomere lengths, indicates that the enzyme is attached to the A-band. The intensity of the fluorescence declines in parallel with dissociation of the enzyme. In this muscle, the number of AMP deaminase binding sites per thick filament is approximately six, suggesting that the enzyme is located at a single axial position in each half A-band. Electron microscopy of negatively stained, antibody-labelled myofibrils reveals the distance between the AMP deaminase sites at opposite ends of an A-band to be 1.69(+/- 0.02 micron). Since the length of the A-band is 1.57 micron, the binding site for the enzyme must be significantly beyond where thick filaments have previously been thought to end.

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Year:  1984        PMID: 6379194     DOI: 10.1016/0022-2836(84)90061-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  11 in total

Review 1.  Genetic analysis of myosin assembly in Caenorhabditis elegans.

Authors:  H F Epstein
Journal:  Mol Neurobiol       Date:  1990 Spring-Summer       Impact factor: 5.590

Review 2.  Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis.

Authors:  T Wallimann; M Wyss; D Brdiczka; K Nicolay; H M Eppenberger
Journal:  Biochem J       Date:  1992-01-01       Impact factor: 3.857

3.  Vertebrate muscle Z-line structure: an electron microscopic study of negatively-stained myofibrils.

Authors:  L A Tskhovrebova
Journal:  J Muscle Res Cell Motil       Date:  1991-10       Impact factor: 2.698

4.  Immunohistochemical localization of histidine-rich glycoprotein in human skeletal muscle: preferential distribution of the protein at the sarcomeric I-band.

Authors:  L Mattii; L Rossi; C Ippolito; G Alì; D Martini; A Raggi; Antonietta R M Sabbatini
Journal:  Histochem Cell Biol       Date:  2017-07-12       Impact factor: 4.304

5.  Assemblages of multiple thick filaments in nematode mutants.

Authors:  H F Epstein; I Ortiz; G C Berliner
Journal:  J Muscle Res Cell Motil       Date:  1987-12       Impact factor: 2.698

6.  Evidence for sequential expression of multiple AMP deaminase isoforms during skeletal muscle development.

Authors:  R Marquetant; N M Desai; R L Sabina; E W Holmes
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

Review 7.  Interaction of creatine kinase and adenylate kinase systems in muscle cells.

Authors:  F Savabi
Journal:  Mol Cell Biochem       Date:  1994 Apr-May       Impact factor: 3.396

8.  Cell-free incorporation of newly synthesized myosin subunits into thick myofilaments.

Authors:  S M Goldfine; S Einheber; D A Fischman
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

9.  Localization of binding sites of F-protein (phosphofructokinase) on the myosin molecule.

Authors:  N A Freydina; M D Shpagina; Z A Podlubnaya
Journal:  J Muscle Res Cell Motil       Date:  1986-12       Impact factor: 2.698

10.  The major myosin-binding domain of skeletal muscle MyBP-C (C protein) resides in the COOH-terminal, immunoglobulin C2 motif.

Authors:  T Okagaki; F E Weber; D A Fischman; K T Vaughan; T Mikawa; F C Reinach
Journal:  J Cell Biol       Date:  1993-11       Impact factor: 10.539

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