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NMR Structural Study of Troponin C C-Terminal Domain Complexed with Troponin I Fragment from Akazara Scallop

  • Fumiaki Yumoto
  • Koji Nagata
  • Kyoko Adachi
  • Nobuaki Nemoto
  • Takao Ojima
  • Kiyoyoshi Nishita
  • Iwao Ohtsuki
  • Masaru Tanokura
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 538)

Abstract

Scallop muscle has been demonstrated to possess both myosin-linked and actin-linked systems1-3 (Fig. 1), even though molluscan muscles were known to be regulated only by the myosin-linked regulatory system mediated through Ca2+-binding to myosin light chains4-6. Recently, the physiological significance of the coexistence of the two systems in scallop adductor muscle was investigated using CDTA-treated scallop myofibrils1. Actin-linked (Troponin-linked) system has been well known as the regulatory system in the muscle contraction of vertebrate striated muscles7. It is regulated by troponin in a Ca2+ dependent manner. Troponin contains three distinct components, i.e., a Ca2+ binding component (TnC), an inhibitory component troponin I (Tnl), and a tropomyosin-binding component troponin T (TnT). TnC contains two independent Ca2+ binding domains, each of which consists of two EF-hand motifs8. Vertebrate striated muscle TnCs bind three or four Ca2+ ions in a molecule and act as the Ca2+ sensor of muscle contraction associated with the binding and release of one or two Ca2+ ion(s) in the N-terminal domain9, 10, 11. The N-terminal domain has, thus, been called the regulatory domain and contains one or two low affinity Ca2+-binding sites (Sites I and II)12. On the other hand, the C-terminal domain has been called the structural domain and contains two high-affinity sites (Sites III and IV). They also bind Mg2+ and are called as Ca2+/Mg2+ sites.

Keywords

Cardiac Troponin Regulatory Light Chain Fast Skeletal Muscle Vertebrate Striate Muscle Skeletal Muscle Troponin 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 2003

Authors and Affiliations

  • Fumiaki Yumoto
    • 1
    • 2
  • Koji Nagata
    • 3
  • Kyoko Adachi
    • 4
  • Nobuaki Nemoto
    • 5
  • Takao Ojima
    • 6
  • Kiyoyoshi Nishita
    • 6
  • Iwao Ohtsuki
    • 2
  • Masaru Tanokura
    • 1
  1. 1.Department of Applied Biological Chemistry, Graduate School of Agricultural and Life SciencesUniversity of TokyoTokyoJapan
  2. 2.School of MedicineThe Jikei UniversityTokyoJapan
  3. 3.Biotechnology Research CenterUniversity of TokyoTokyoJapan
  4. 4.Marine Biotechnology InstituteShizuokaJapan
  5. 5.Varian Technologies JapanTokyoJapan
  6. 6.Laboratory of Biochemistry and Biotechnology, Graduate School of Fisheries ScienceHokkaido UniversityHakodate, HokkaidoJapan

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