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The interaction of cations with the calcium-binding site of troponin

1970; Elsevier BV; Volume: 221; Issue: 2 Linguagem: Inglês

10.1016/0005-2795(70)90290-4

1878-1454

Franklin Fuchs, Y. Jayasudhan Reddy, F. Norman Briggs,

Chromatography in Natural Products

Understanding the process of Ca2+/Mg2+exchange during muscle excitation and relaxation is fundamental to elucidating the mechanism of Ca2+-regulated muscle contraction. During the resting phase, the C-domain of cardiac troponin C may be occupied by either Ca2+or Mg2+. Here, complexes of recombinant cardiac troponin C(81–161) and the N terminus of cardiac troponin I, representing residues 33–80, were generated in the presence of saturating Mg2+. Heteronuclear multi-dimensional nuclear magnetic resonance experiments were used to obtain backbone assignments of the Mg2+-loaded complex. In the presence of cardiac troponin I, the affinity of site IV for Mg2+is increased. Comparison of Mg2+and Ca2+-loaded complexes reveals that chemical shift differences are primarily localized to metal-binding sites III and IV, defining positions within these sites that have distinct Ca2+/Mg2+conformations. The observed transition from the Mg2+-loaded to Ca2+-loaded form demonstrates that sites III and IV fill simultaneously with Ca2+displacing Mg2+. However, even in the absence of excess Ca2+, Mg2+does not readily displace Ca2+in the isolated binary complex. Thus, the Mg2+-loaded conformer may only represent a small fraction of the total cardiac troponin C found in the sarcomere.