Freitag, 21. April 2017, 07:00 - 07:00 iCal
Guest Lecture by Prof. Raimund DUTZLER/Uni Zurich
“Mechanistic relationships in the TMEM16 family of calcium activated
chloride channels and lipid scramblases”
IST-Austria, Big Seminar Room, Building West
Am Campus 1, 3400 Klosterneuburg
Lecture
The Doctoral Program
ION CHANNELS AND TRANSPORTERS AS MOLECULAR DRUG TARGETS („MolTag“) is pleased to invite you to the following lecture
“Mechanistic relationships in the TMEM16 family of calcium activated
chloride channels and lipid scramblases”
by Prof.Dr. Raimund DUTZLER, Department of Biochemistry, University of Zurich. tinyurl.com/glrp3ah, dutzler@bioc.uzh.ch
on: Friday, April 21st 2017, 03:00 pm (15:00 Uhr)
at: IST-AUSTRIA, Big Seminar Room in Building West
Abstract:.
The TMEM16 proteins constitute a family of membrane proteins with an unusual functional breadth, which includes lipid scramblases and Cl- channels. Both functional branches are activated by calcium, acting from the intracellular side, and they share a common architecture, which was defined by the structure of the lipid scramblase nhTMEM16 (1). In this protein, each subunit of the homo-dimeric protein encompasses ten transmembrane helices and structured cytosolic domains. The structural features of subunits suggest that the dimeric protein harbors two locations for catalysis that are independent with respect to activation and lipid conduction. In scramblases, the ‘subunit cavity’, a hydrophilic membrane-traversing furrow contained within each subunit that is exposed to the lipid bilayer provides a path for polar lipid headgroups across the membrane. It contains a conserved Ca2+-binding site located within the hydrophobic core of the membrane, which regulates activation in both channels and scramblases. As shown by electrophysiology the ion channel TMEM16A contains two ion conduction pores that are independently activated by Ca2+ (2). The nhTMEM16 structure thus provides insight into functional mechanisms underlying lipid movement in scramblases and ion conduction in channels of the TMEM16 family.
1. J. D. Brunner, N. K. Lim, S. Schenck, A. Duerst, R. Dutzler, X-ray structure of a calcium-activated TMEM16 lipid scramblase. Nature 516, 207-212 (2014).
2. N. K. Lim, A. K. Lam, R. Dutzler, Independent activation of ion conduction pores in the double-barreled calcium-activated chloride channel TMEM16A. J Gen Physiol 148, 375-392 (2016).
Contact: Doctoral Program MolTag, Dept. of Pharmacology and Toxicology; moltag.univie.ac.at, Office.moltag@univie.ac.at
Zur Webseite der Veranstaltung
Veranstalter
Doktoratskolleg Molecular Drug Targets, "MolTag"
Kontakt
Susanne Menschik-Zunzer
Department of Pharmacology and Toxicology
DK Molecular Drug Targets
01 5277 55320
susanne.menschik-zunzer@univie.ac.at, office.moltag@univie.ac.at
Erstellt am Montag, 06. Mrz 2017, 09:44
Letzte Änderung am Dienstag, 07. Mrz 2017, 13:50