Open AccessChemistryBiologyMedicine

John Limouze, A. Straight, T. Mitchison, J. Sellers

2004JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

DOI: 10.1007/s10974-004-6060-7

tlooto Summary

The specificity and potency of Blebbistatin are examined by assaying its effects on the actin-activated MgATPase assay of diverse members of the myosin superfamily, and smooth muscle which is highly homologous to vertebrate nonmuscle myOSin is only poorly inhibited.

Abstract

Blebbistatin is a small molecule inhibitor discovered in a screen for inhibitors of nonmuscle myosin IIA. We have examined the specificity and potency of the drug by assaying its effects on the actin-activated MgATPase assay of diverse members of the myosin superfamily. Blebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 values ranging from 0.5 to 5 μM. Interestingly, smooth muscle which is highly homologous to vertebrate nonmuscle myosin is only poorly inhibited (IC50=80 μM). The drug potently inhibits Dictyostelium myosin II, but poorly inhibits Acanthamoeba myosin II. Blebbistatin did not inhibit representative myosin superfamily members from classes I, V, and X.

Citation format

LIMOUZE, John, et al. Specificity of blebbistatin, an inhibitor of myosin II. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 2004, 25: 337–341.