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Savannah J. West

Researcher at University of Texas Health Science Center at Houston

Publications -  10
Citations -  59

Savannah J. West is an academic researcher from University of Texas Health Science Center at Houston. The author has contributed to research in topics: STIM1 & Acylation. The author has an hindex of 2, co-authored 6 publications receiving 25 citations. Previous affiliations of Savannah J. West include University of Texas MD Anderson Cancer Center & University of South Alabama.

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Journal ArticleDOI

Spectral imaging of FRET-based sensors reveals sustained cAMP gradients in three spatial dimensions.

TL;DR: Results demonstrate that spectral imaging approaches can be used to assess cAMP gradients—and in general gradients in fluorescence and FRET—within intact cells, and demonstrate that 2D imaging studies of localized fluorescence signals and, in particular, cAMP signals may lead to erroneous conclusions about the existence and/or magnitude ofgradients in either FRET or the underlying cAMP messages.
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Detection of Protein S-Acylation using Acyl-Resin Assisted Capture

TL;DR: Acyl-RAC as discussed by the authors is a recently developed method based on selective capture of endogenously S-acylated proteins by thiol-reactive Sepharose beads, which requires fewer steps and can yield more reliable results when coupled with mass spectrometry for identification of novel Sacylation targets.
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S-acylation of Orai1 regulates store-operated Ca2+ entry.

TL;DR: In this article, the authors show that Orai1 is rapidly S-acylated at cysteine 143 upon ER Ca2+ store depletion, leading to the formation of activated CRAC channels.
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Ca2+-dependent protein acyltransferase DHHC21 controls activation of CD4+ T cells

TL;DR: In this paper, the authors demonstrate that DHHC21, a member of the DHHC family of mammalian protein acyltransferases, mediates T cell receptor-induced S-acylation of proximal T cell signaling proteins.
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Dynamic S-acylation of the ER-resident protein stromal interaction molecule 1 (STIM1) is required for store-operated Ca2+ entry

TL;DR: In this paper , it was shown that S-acylation of Orai1 is dynamically regulated in a stimulus-dependent manner and essential for its function as a calcium channel.