Membrane crystals of Ca2+-ATPase in sarcoplasmic reticulum of normal and dystrophic muscle.

Two-dimensional crystalline arrays of the Ca2+ transport ATPase develop after treatment of sarcoplasmic reticulum vesicles with Na3VO4. The dimensions of the crystal lattice are similar in sarcoplasmic reticulum membranes isolated from normal and genetically dystrophic human, mouse, and chicken muscles. These observations indicate similar requirements for ATPase-ATPase interactions in sarcoplasmic reticulum of normal and dystrophic muscles and lessen the likelihood of a molecular defect of the Ca2+ pump in the various forms of genetic muscular dystrophies.