A new method for the time-resolved measurement of phosphate release in permeabilized muscle fibers.
- 1 April 1995
- journal article
- Vol. 68, 191S-193S
Abstract
A new method for the measurement of phosphate release in contracting and relaxed permeabilized muscle fibers is described. The assay is based on a genetically engineered phosphate-binding protein labeled with a coumarin fluorescent probe, which binds inorganic phosphate tightly and shows a fourfold increase in fluorescence upon binding. Measurements of Pi release on the millisecond time scale with sensitivity in the 10 microM range are obtained that provide new information about the relationship between ATP hydrolysis and force production.This publication has 2 references indexed in Scilit:
- Direct, Real-Time Measurement of Rapid Inorganic Phosphate Release Using a Novel Fluorescent Probe and Its Application to Actomyosin Subfragment 1 ATPaseBiochemistry, 1994
- Myofibrillar ATPase activity and mechanical performance of skinned fibres from rabbit psoas muscle.The Journal of Physiology, 1994