The study provides evidence that monomeric Ca2+-ATPase undergoes conformational changes during the Ca2+ pumping cycle independent of a phospholipid bilayer.
Answers are grounded in this paper and cite their sources.
Supports bilayer-independent Ca2+-ATPase conformational changes; hypothesis-generating for cardiac SR calcium handling, requiring intact-system validation.
The kinetics and extent of the fluorescence change induced by Ca2+ interaction with the Ca2+-ATPase from sarcoplasmic reticulum have been compared by stopped flow fluorimetry for three preparations: sarcoplasmic reticulum; purified ATPase in membrane vesicles; and solubilized, delipidated ATPase. The kinetics of Ca2+ release and binding for both purified preparations could be described by a single exponential as has been observed for sarcoplasmic reticulum. The rate and extent of the fluorescence change for the solubilized and membrane-associated preparations are shown to be quite similar to those of the sarcoplasmic reticulum. From these results, it is concluded that all of the Ca2+-induced fluoescence change in sarcoplasmic reticulum originates from the Ca2+-ATPase. In addition, since the change in fluorescence is probably result of a conformational change in the ATPase during the Ca2+ pumping cycle, the results provide additional evidence that monomeric Ca2+-ATPase may be capable of Ca2+ transport since the delipidated preparation is monomeric under the conditions used for these experiments. Finally, it is concluded that phospholipid bilayer is not essential for this conformational change.
No takes yet. Share an insight, caveat, or question.
Dean et al. (1980) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: