Title

Myosin Va becomes a low duty ratio motor in the inhibited form

UMMS Affiliation

Department of Physiology

Publication Date

3-17-2007

Document Type

Article

Subjects

Actins; Adenosine Diphosphate; Adenosine Triphosphate; Animals; Calcium; Egtazic Acid; Enzyme Activation; Humans; Hydrolysis; Kinetics; Mice; Myosin Heavy Chains; Myosin Type V; Protein Binding; *Protein Folding; Recombinant Proteins

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Vertebrate myosin Va is a typical processive motor with high duty ratio. Recent studies have revealed that the actin-activated ATPase activity of the full-length myosin Va (M5aFull) is inhibited at a low [Ca(2+)], which is due to the formation of a folded conformation of M5aFull. To clarify the underlying inhibitory mechanism, we analyzed the actin-activated ATP hydrolysis mechanism of the M5aFull at the inhibited and the activated states, respectively. Marked differences were found in the hydrolysis, P(i) release, and ADP release steps between the activated and the inhibited states. The kinetic constants of these steps of the activated state were similar to those of the unregulated S1 construct, in which the rate-limiting step was the ADP release step. On the other hand, the P(i) release rate from acto-M5aFull was decreased in EGTA by >1,000-fold, which makes this step the rate-limiting step for the actin-activated ATP hydrolysis cycle of M5aFull. The ADP off rate from acto-M5aFull was decreased by approximately 10-fold, and the equilibrium between the prehydrolysis state and the post hydrolysis state was shifted toward the former state in the inhibited state of M5aFull. Because of these changes, M5aFull spends a majority of the ATP hydrolysis cycling time in the weak actin binding state. The present results indicate that M5aFull molecules at a low [Ca(2+)] is inhibited as a cargo transporter not only due to the decrease in the cross-bridge cycling rate but also due to the decrease in the duty ratio thus being dissociated from actin.

Rights and Permissions

Citation: J Biol Chem. 2007 May 4;282(18):13228-39. Epub 2007 Mar 14. Link to article on publisher's site

DOI of Published Version

10.1074/jbc.M610766200

Related Resources

Link to Article in PubMed

Journal/Book/Conference Title

The Journal of biological chemistry

PubMed ID

17363376