Ca2+-insensitive contraction in glycerinated skeletal muscle fiber treated with additional troponin T.

Abstract

An investigation was carried out on the effect of troponin T (TnT) protein on the Ca2+-sensitivity of fiber contraction when it was added to glycerinated muscle fiber. The TnT-treated fiber was observed to lose its Ca2+ -sensitivity, so that it was seen to contract even ina Ca2+ -free buffer solution. However, the treated fibers were not significantly different from the normally glycerinated ones in terms of tension magnitude. On the other hand, the fiber did not lose its Ca2+ -sensitivity upon treatment in a similar manner with trophin I (TnI) or troponin C (TnC) protein instead of TnT; the tension magnitude was seen to decrease only with the TnI treatment. SDS-PAGE patterns of the TnT-treated fibers were different from those of glycerinated ones at the TnI and TnC band, which were fainter in the TnT-treated fibers than in normal ones. DACM-labeled fibers also decreased in the DACM-labeled TnI and TnC proteins on gel as a result of the treatment with TnT protein. Further, those proteins were completely removed from fibers into extra medium. These findings suggest that the additional TnT protein removes TnI and TnC subunits from the troponin (Tn) complex combined with thin filaments in the fibers, or that it exchanges the total Tn complex on the thin filaments.