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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Studies of Ca2+ ATPase (SERCA) inhibition.

The Ca(2+) transport ATPase of intracellular membranes (SERCA) can be inhibited by a series of chemical compounds such as Thapsigargin (TG), 2,5-di(tert-butyl)hydroquinone (DBHQ) and 1,3-dibromo-2,4,6-tris (methyl-isothio-uronium) benzene (Br(2)-TITU). These compounds have specific binding sites in the ATPase protein, and different mechanisms of inhibition. On the other hand, SERCA gene silencing offers a convenient and specific method for suppression of SERCA activity in cells. The physiological and pharmacological implications of SERCA inhibition are discussed.[1]

References

  1. Studies of Ca2+ ATPase (SERCA) inhibition. Inesi, G., Hua, S., Xu, C., Ma, H., Seth, M., Prasad, A.M., Sumbilla, C. J. Bioenerg. Biomembr. (2005) [Pubmed]
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