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Crosslinking of telokin to chicken gizzard smooth muscle myosin.

Crosslinking of telokin to chicken gizzard smooth muscle myosin. Research Abstract Details 

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  • Crosslinking of telokin to chicken gizzard smooth muscle myosin. Abstract Text:

    t masatoT Masato,t numataT Numata,t katohT Katoh,f moritaF Morita,m yazawaM Yazawa,

    Telokin, which is a candidate for one of the factors stabilizing dephosphorylated myosin filaments in smooth muscle cells, was subjected to a chemical crosslinking study to determine its binding location on the myosin molecule. Telokin labeled with 5-iodoacetamidofluorescein (Fl-telokin) retained the nature of unlabeled telokin: it bound to dephosphorylated gizzard myosin with a stoichiometry of 1 mol/mol myosin and induced filament assembly. The carboxyl groups of Fl-telokin were activated with 1-ethyl-3-(3-dimethyl-amino-propyl) carbodiimide and N-hydroxysuccinimide and then crosslinked to myosin. The production of three fluorescent peptides was observed on an SDS-gel, accompanying a decrease in the amount of regulatory light chain (LC20). The molecular weights of these products estimated to be > 200, 62, and 41 kDa. When unlabeled telokin was crosslinked to myosin of which LC20 was exchanged with 5-[[2-[(iodoacetyl)amino]ethyl]amino]-naphthalene-1-sulfonic acid-labeled LC20, the 62- and 41-kDa bands were also fluorescent. These results suggest that the > 200, 62, and 41-kDa species are telokin crosslinked with a heavy chain, with 2 LC20, and with 1 LC20, respectively. Myosin crosslinked with unlabeled telokin showed an extra structure with a small projection at the head-rod junction on electron microscopy and this structure was proved to be telokin by decorating it with anti-telokin antibodies. In addition, dephosphorylated myosin crosslinked with Fl-telokin was incapable of folding into the 10S conformation at 0.2 NaCl in the presence of MgATP, and assembled into filaments at 0.15 M NaCl in the presence of MgATP. Thus, telokin may bind to LC20 and a heavy chain region at the head-rod junction and suppress folding into the 10S conformation, leading to the assembly of myosin into filaments.

    Crosslinking of telokin to chicken gizzard smooth muscle myosin. Publishing Authors By Initials

    t masatoT Masato,t numataT Numata,t katohT Katoh,f moritaF Morita,m yazawaM Yazawa,

    For similar organic chemicals: imides: succinimides research abstracts see: organic chemicals: imides: succinimides research

    PUBMED ID PMID:

    MEDLINE DATE:

    Crosslinking of telokin to chicken gizzard smooth muscle myosin. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of biochemistry

    VOLUME: 121

    Page Numbers: 225-30

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 19

    MONTH: Feb

    YEAR: 1997

    Crosslinking of telokin to chicken gizzard smooth muscle myosin. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Crosslinking of telokin to chicken gizzard smooth muscle myosin. Keywords Mesh Terms:

    KEYWORDS: Succinimides

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Crosslinking of telokin to chicken gizzard smooth muscle myosin. Information

    Substance Name: Myosins

    Registry Number: EC 3.6.1.4

    Grant and Affiliation Information for Crosslinking of telokin to chicken gizzard smooth muscle myosin.

    AFFILIATION: Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo.

    Country: JAPAN

    JAPAN Research PublicationJAPAN Research Publication

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    MEDLINETA: J Biochem

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