Trevor John Shuttleworth, Ph.D.
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Contact
University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, Box 711
Rochester, New York 14642
Office: 585 275-2076 (primary)
Lab: 585 275-3431
Fax: 585 273-2652

The cellular actions of many neurotransmitters and hormones are dependent on receptor-activated increases in intracellular calcium concentrations in their target cells. In various secretory and other "non-excitable" cells, the physiologically relevant signals often take the form of a series of Ca2+ oscillations, and many critical cellular responses are tuned to respond to the specific frequency of such oscillations. A key factor in sustaining these signals and determining their frequency, is the receptor-activated entry of Ca2+ from the extracellular medium. Our research concerns the nature of the conductances responsible for this entry, and their specific roles in modulating the overall Ca2+ signal. Specifically, our recent research has focused on the ARC channel – a novel Ca2+ entry channel that is activated by the receptor-mediated generation of arachidonic acid, and which we first described a few years ago. Importantly, it is this channel that appears to play the major role in the entry of Ca2+ during the generation of the oscillatory Ca2+ signals in several cell types. We have recently characterized the key molecular components of this channel, revealing that it is a member of a new family of channels – the "Orai-based channels". This molecular characterization has opened up new opportunities for the analysis of its nature, mechanism of activation, and regulation. This, along with identifying how the Ca2+ entering via this channel acts to modulate the frequency of the agonist-induced Ca2+ oscillations, forms the major focus of our current research.
Techniques used include patch-clamp analysis of ion-channel activity, digital imaging, real-time confocal imaging, and photon-counting microfluorimetric measurements of intracellular Ca2+ concentrations in single cells, and biochemical and molecular studies of the proteins that form the channel and its regulators.
Current Appointments
- Professor - Department of Pharmacology and Physiology (SMD)
- Professor - Center for Oral Biology (SMD)
| Education | ||
|---|---|---|
| PhD Zoology/Comp. Physiology | New Zealand-Univ of Otago | 1972 |
| BS Zoology | UK-Univ of London | 1968 |
| Post-Doctoral Training & Residency | |
|---|---|
| SRC Research Associate, Department of Biological Sciences, University of Lancaster, England | 1972 - 1974 |
| Recent Journal Articles |
|---|
| Showing the 5 most recent journal articles. (89 available) |
| Shuttleworth TJ. "Arachidonic acid, ARC channels, and Orai proteins." Cell calcium. 2009; Epub 2009 Mar 09. |
| Mignen O; Thompson JL; Shuttleworth TJ. "The molecular architecture of the arachidonate-regulated Ca2+-selective ARC channel is a pentameric assembly of Orai1 and Orai3 subunits." The Journal of physiology. 2009; Epub 2009 Jul 21. |
| Mignen O; Thompson JL; Shuttleworth TJ. "Both Orai1 and Orai3 are essential components of the arachidonate-regulated Ca2+-selective (ARC) channels." The Journal of physiology. 2008; 586(1):185-95. Epub 2007 Nov 08. |
| Mignen O; Thompson JL; Shuttleworth TJ. "Orai1 subunit stoichiometry of the mammalian CRAC channel pore." The Journal of physiology. 2008; 586(2):419-25. Epub 2007 Nov 15. |
| Thompson JL; Mignen O; Shuttleworth TJ. "The Orai1 SCID mutation and CRAC channel function in the heterozygous condition." The Journal of biological chemistry. 2008; Epub 2008 Dec 15. |

