Abstract
Direct measurements of the stiffness (elastic bending resistance) of demembranated sea urchin sperm flagella were made in the presence of MgATP2- and vanadate. Under these conditions the flagellum is in a relaxed state, with a stiffness of .apprx. 0.9 .times. 10-21 N m2, which is .apprx. 5% of the stiffness obtained in the rigor state in the absence of MgATP2-. MgADP- does not substitute for MgATP2- in producing the relaxed state. A progressive inhibition of movement is observed after addition of MgATP2- to flagella preincubated with vanadate, in which new bend generation, propagation and relaxation by straightening are distinguished, depending on the ratio of MgATP2- and vanadate. At appropriate concentrations of vanadate, increase of the velocity of bend propagation is observed at a very low concentration of MgATP2- that is not enough to induce spontaneous beating. Vanadate enhances competitive inhibition of beat frequency by MgADP- but not by ADP3-, ATP4- or Pi. These observations and the uncompetitive inhibition of beat frequency by vanadate indicate that vanadate can only bind to dynein-nucleotide complexes induced by MgATP2- and MgADP-. The state accessible by MgATP2- binding must be a state in which the cross-bridges are detached and the flagellum is relaxed. The state accessible by MgADP- binding must be a cross-bridged state. Bound vanadate prevents the transition between these 2 states. Inhibition and relaxation by vanadate in the presence of MgATP2- results from the specific affinity of vanadate for a state in which nucleotide is bound, rather than a specific affinity for the detached state.