New Techniques for Studying Calcium Gradients

Abstract

Improved techniques for detecting and manipulating spatial gradients of cytosolic free Ca(2+) concentrations (Ca(2)) sub i and intracellular stores are discussed. Three areas of progress are: (1) development of new fluorescent indicators for Ca(2+) that are the first to be suitable for measuring Ca(2+)) sub i and its inhomogeneities in individual cells; (2) invention of photolabile chelators which shift irreversibly from high to low affinity for Ca(2+) upon illumination, permitting light-controlled jumps in (Ca(2+)) sub i; and (3) fixation methods to trap dynamic intraorganellar Ca stores in a form readily visible by electron microscopy.