Papers associated with asic1

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	Diarylamidines: high potency inhibitors of acid-sensing ion channels., Chen X, Qiu L, Li M, Dürrnagel S, Orser BA, Xiong ZG, MacDonald JF., Neuropharmacology. June 1, 2010; 58 (7): 1045-53.
	Two residues in the extracellular domain convert a nonfunctional ASIC1 into a proton-activated channel., Li T, Yang Y, Canessa CM., Am J Physiol Cell Physiol. July 1, 2010; 299 (1): C66-73.
	Leu85 in the beta1-beta2 linker of ASIC1 slows activation and decreases the apparent proton affinity by stabilizing a closed conformation., Li T, Yang Y, Canessa CM., J Biol Chem. July 16, 2010; 285 (29): 22706-12.
	Proteolytic cleavage of human acid-sensing ion channel 1 by the serine protease matriptase., Clark EB, Jovov B, Rooj AK, Fuller CM, Benos DJ., J Biol Chem. August 27, 2010; 285 (35): 27130-43.
	Asn415 in the beta11-beta12 linker decreases proton-dependent desensitization of ASIC1., Li T, Yang Y, Canessa CM., J Biol Chem. October 8, 2010; 285 (41): 31285-91.
	Identification of a calcium permeable human acid-sensing ion channel 1 transcript variant., Hoagland EN, Sherwood TW, Lee KG, Walker CJ, Askwith CC., J Biol Chem. December 31, 2010; 285 (53): 41852-62.
	Outlines of the pore in open and closed conformations describe the gating mechanism of ASIC1., Li T, Yang Y, Canessa CM., Nat Commun. January 1, 2011; 2 399.
	Asp433 in the closing gate of ASIC1 determines stability of the open state without changing properties of the selectivity filter or Ca2+ block., Li T, Yang Y, Canessa CM., J Gen Physiol. March 1, 2011; 137 (3): 289-97.
	Identification of the roles of conserved charged residues in the extracellular domain of an epithelial sodium channel (ENaC) subunit by alanine mutagenesis., Edelheit O, Hanukoglu I, Dascal N, Hanukoglu A., Am J Physiol Renal Physiol. April 1, 2011; 300 (4): F887-97.
	Base of the thumb domain modulates epithelial sodium channel gating., Shi S, Ghosh DD, Okumura S, Carattino MD, Kashlan OB, Sheng S, Kleyman TR., J Biol Chem. April 29, 2011; 286 (17): 14753-61.
	Insights into the mechanism of pore opening of acid-sensing ion channel 1a., Tolino LA, Okumura S, Kashlan OB, Carattino MD., J Biol Chem. May 6, 2011; 286 (18): 16297-307.
	Heteromeric acid-sensing ion channels (ASICs) composed of ASIC2b and ASIC1a display novel channel properties and contribute to acidosis-induced neuronal death., Sherwood TW, Lee KG, Gormley MG, Askwith CC., J Neurosci. June 29, 2011; 31 (26): 9723-34.
	The interaction between two extracellular linker regions controls sustained opening of acid-sensing ion channel 1., Springauf A, Bresenitz P, Gründer S., J Biol Chem. July 8, 2011; 286 (27): 24374-84.
	Cross-reactivity of acid-sensing ion channel and Na⁺-H⁺ exchanger antagonists with nicotinic acetylcholine receptors., Santos-Torres J, Ślimak MA, Auer S, Ibañez-Tallon I., J Physiol. November 1, 2011; 589 (Pt 21): 5109-23.
	A heteromeric Texas coral snake toxin targets acid-sensing ion channels to produce pain., Bohlen CJ, Chesler AT, Sharif-Naeini R, Medzihradszky KF, Zhou S, King D, Sánchez EE, Burlingame AL, Basbaum AI, Julius D., Nature. November 16, 2011; 479 (7373): 410-4.
	N-glycosylation of acid-sensing ion channel 1a regulates its trafficking and acidosis-induced spine remodeling., Jing L, Chu XP, Jiang YQ, Collier DM, Wang B, Jiang Q, Snyder PM, Zha XM., J Neurosci. March 21, 2012; 32 (12): 4080-91.
	Contribution of residues in second transmembrane domain of ASIC1a protein to ion selectivity., Carattino MD, Della Vecchia MC., J Biol Chem. April 13, 2012; 287 (16): 12927-34.
	Lignan from thyme possesses inhibitory effect on ASIC3 channel current., Dubinnyi MA, Osmakov DI, Koshelev SG, Kozlov SA, Andreev YA, Zakaryan NA, Dyachenko IA, Bondarenko DA, Arseniev AS, Grishin EV., J Biol Chem. September 21, 2012; 287 (39): 32993-3000.
	High Ca(2+) permeability of a peptide-gated DEG/ENaC from Hydra., Dürrnagel S, Falkenburger BH, Gründer S., J Gen Physiol. October 1, 2012; 140 (4): 391-402.
	Subtype-specific modulation of acid-sensing ion channel (ASIC) function by 2-guanidine-4-methylquinazoline., Alijevic O, Kellenberger S., J Biol Chem. October 19, 2012; 287 (43): 36059-70.
	Black mamba venom peptides target acid-sensing ion channels to abolish pain., Diochot S, Baron A, Salinas M, Douguet D, Scarzello S, Dabert-Gay AS, Debayle D, Friend V, Alloui A, Lazdunski M, Lingueglia E., Nature. October 25, 2012; 490 (7421): 552-5.
	Impact of recovery from desensitization on acid-sensing ion channel-1a (ASIC1a) current and response to high frequency stimulation., Li T, Yang Y, Canessa CM., J Biol Chem. November 23, 2012; 287 (48): 40680-9.
	Gating transitions in the palm domain of ASIC1a., Della Vecchia MC, Rued AC, Carattino MD., J Biol Chem. February 22, 2013; 288 (8): 5487-95.
	Conformational changes in the lower palm domain of ASIC1a contribute to desensitization and RFamide modulation., Frey EN, Pavlovicz RE, Wegman CJ, Li C, Askwith CC., PLoS One. August 12, 2013; 8 (8): e71733.
	Independent contribution of extracellular proton binding sites to ASIC1a activation., Krauson AJ, Rued AC, Carattino MD., J Biol Chem. November 29, 2013; 288 (48): 34375-83.
	Protonation controls ASIC1a activity via coordinated movements in multiple domains., Bonifacio G, Lelli CI, Kellenberger S., J Gen Physiol. January 1, 2014; 143 (1): 105-18.
	The bile acid-sensitive ion channel (BASIC) is activated by alterations of its membrane environment., Schmidt A, Lenzig P, Oslender-Bujotzek A, Kusch J, Lucas SD, Gründer S, Wiemuth D., PLoS One. January 1, 2014; 9 (10): e111549.
	Acid-sensing ion channel (ASIC) 1a/2a heteromers have a flexible 2:1/1:2 stoichiometry., Bartoi T, Augustinowski K, Polleichtner G, Gründer S, Ulbrich MH., Proc Natl Acad Sci U S A. June 3, 2014; 111 (22): 8281-6.
	Ion conduction and selectivity in acid-sensing ion channel 1., Yang L, Palmer LG., J Gen Physiol. September 1, 2014; 144 (3): 245-55.
	Intersubunit conformational changes mediate epithelial sodium channel gating., Collier DM, Tomkovicz VR, Peterson ZJ, Benson CJ, Snyder PM., J Gen Physiol. October 1, 2014; 144 (4): 337-48.
	The comprehensive analysis of DEG/ENaC subunits in Hydra reveals a large variety of peptide-gated channels, potentially involved in neuromuscular transmission., Assmann M, Kuhn A, Dürrnagel S, Holstein TW, Gründer S., BMC Biol. October 14, 2014; 12 84.
	Tarantula toxins use common surfaces for interacting with Kv and ASIC ion channels., Gupta K, Zamanian M, Bae C, Milescu M, Krepkiy D, Tilley DC, Sack JT, Yarov-Yarovoy V, Kim JI, Swartz KJ., Elife. January 6, 2015; 4 e06774.
	Xenopus borealis as an alternative source of oocytes for biophysical and pharmacological studies of neuronal ion channels., Cristofori-Armstrong B, Soh MS, Talwar S, Brown DL, Griffin JD, Dekan Z, Stow JL, King GF, Lynch JW, Rash LD., Sci Rep. January 12, 2015; 5 14763.
	Extracellular Subunit Interactions Control Transitions between Functional States of Acid-sensing Ion Channel 1a., Gwiazda K, Bonifacio G, Vullo S, Kellenberger S., J Biol Chem. July 17, 2015; 290 (29): 17956-17966.
	The Human Acid-Sensing Ion Channel ASIC1a: Evidence for a Homotetrameric Assembly State at the Cell Surface., van Bemmelen MX, Huser D, Gautschi I, Schild L., PLoS One. August 4, 2015; 10 (8): e0135191.
	Molecular dynamics and functional studies define a hot spot of crystal contacts essential for PcTx1 inhibition of acid-sensing ion channel 1a., Saez NJ, Deplazes E, Cristofori-Armstrong B, Chassagnon IR, Lin X, Mobli M, Mark AE, Rash LD, King GF., Br J Pharmacol. October 1, 2015; 172 (20): 4985-95.
	Optogenetic approaches addressing extracellular modulation of neural excitability., Ferenczi EA, Vierock J, Atsuta-Tsunoda K, Tsunoda SP, Ramakrishnan C, Gorini C, Thompson K, Lee SY, Berndt A, Perry C, Minniberger S, Vogt A, Mattis J, Prakash R, Delp S, Deisseroth K, Hegemann P., Sci Rep. January 22, 2016; 6 23947.
	Mambalgin-1 Pain-relieving Peptide, Stepwise Solid-phase Synthesis, Crystal Structure, and Functional Domain for Acid-sensing Ion Channel 1a Inhibition., Mourier G, Salinas M, Kessler P, Stura EA, Leblanc M, Tepshi L, Besson T, Diochot S, Baron A, Douguet D, Lingueglia E, Servent D., J Biol Chem. February 5, 2016; 291 (6): 2616-29.
	Analgesic effects of mambalgin peptide inhibitors of acid-sensing ion channels in inflammatory and neuropathic pain., Diochot S, Alloui A, Rodrigues P, Dauvois M, Friend V, Aissouni Y, Eschalier A, Lingueglia E, Baron A., Pain. March 1, 2016; 157 (3): 552-559.
	The Thumb Domain Mediates Acid-sensing Ion Channel Desensitization., Krauson AJ, Carattino MD., J Biol Chem. May 20, 2016; 291 (21): 11407-19.
	Functional and pharmacological characterization of two different ASIC1a/2a heteromers reveals their sensitivity to the spider toxin PcTx1., Joeres N, Augustinowski K, Neuhof A, Assmann M, Gründer S., Sci Rep. June 9, 2016; 6 27647.
	Activation of the Human Epithelial Sodium Channel (ENaC) by Bile Acids Involves the Degenerin Site., Ilyaskin AV, Diakov A, Korbmacher C, Haerteis S., J Biol Chem. September 16, 2016; 291 (38): 19835-47.
	Ca2+ permeability and Na+ conductance in cellular toxicity caused by hyperactive DEG/ENaC channels., Matthewman C, Miller-Fleming TW, Miller DM, Bianchi L., Am J Physiol Cell Physiol. December 1, 2016; 311 (6): C920-C930.
	Bile acids potentiate proton-activated currents in Xenopus laevis oocytes expressing human acid-sensing ion channel (ASIC1a)., Ilyaskin AV, Diakov A, Korbmacher C, Haerteis S., Physiol Rep. February 1, 2017; 5 (3):
	A selectivity filter at the intracellular end of the acid-sensing ion channel pore., Lynagh T, Flood E, Boiteux C, Wulf M, Komnatnyy VV, Colding JM, Allen TW, Pless SA., Elife. May 12, 2017; 6
	An implantable ENG detector with in-system velocity selective recording (VSR) capability., Clarke C, Rieger R, Schuettler M, Donaldson N, Taylor J., Med Biol Eng Comput. June 1, 2017; 55 (6): 885-895.
	Pharmacological modulation of Acid-Sensing Ion Channels 1a and 3 by amiloride and 2-guanidine-4-methylquinazoline (GMQ)., Besson T, Lingueglia E, Salinas M., Neuropharmacology. October 1, 2017; 125 429-440.
	Molecular Basis for Allosteric Inhibition of Acid-Sensing Ion Channel 1a by Ibuprofen., Lynagh T, Romero-Rojo JL, Lund C, Pless SA., J Med Chem. October 12, 2017; 60 (19): 8192-8200.
	Diminazene Is a Slow Pore Blocker of Acid-Sensing Ion Channel 1a (ASIC1a)., Schmidt A, Rossetti G, Joussen S, Gründer S., Mol Pharmacol. December 1, 2017; 92 (6): 665-675.
	Discovery and molecular interaction studies of a highly stable, tarantula peptide modulator of acid-sensing ion channel 1., Er SY, Cristofori-Armstrong B, Escoubas P, Rash LD., Neuropharmacology. December 1, 2017; 127 185-195.

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