Movement of NH3 through the human urea transporter B: a new gas channel


Autoria(s): Geyer, R. Ryan; Aziz, Raif Musa; Enkavi, Giray; Mahinthichaichan, P.; Tajkhorshid, Emad; Boron, Walter F.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

28/03/2014

28/03/2014

15/06/2013

Resumo

Aquaporins and Rh proteins can function as gas (CO2 and NH3) channels. The present study explores the urea, H2O, CO2, and NH3 permeability of the human urea transporter B (UT-B) (SLC14A1), expressed in Xenopus oocytes. We monitored urea uptake using [14C]urea and measured osmotic water permeability (Pf) using video microscopy. To obtain a semiquantitative measure of gas permeability, we used microelectrodes to record the maximum transient change in surface pH (∆pHS) caused by exposing oocytes to 5% CO2/33 mM HCO3- (pHS increase) or 0.5 mM NH3/NH4+ (pHS decrease). UT-B expression increased oocyte permeability to urea by >20-fold, and Pf by 8-fold vs. H2O-injected control oocytes. UT-B expression had no effect on the CO2-induced ∆pHS but doubled the NH3-induced ∆pHS. Phloretin reduced UT-B-dependent urea uptake (Jurea * ) by 45%, Pf * by 50%, and (- ∆pHS * )NH3 by 70%. p-Chloromercuribenzene sulfonate reduced Jurea * by 25%, Pf * by 30%, and (∆pHS * )NH3 by 100%. Molecular dynamics (MD) simulations of membrane-embedded models of UT-B identified the monomeric UT-B pores as the main conduction pathway for both H2O and NH3 and characterized the energetics associated with permeation of these species through the channel. Mutating each of two conserved threonines lining the monomeric urea pores reduced H2O and NH3 permeability. Our data confirm that UT-B has significant H2O permeability and for the first time demonstrate significant NH3 permeability. Thus the UTs become the third family of gas channels. Inhibitor and mutagenesis studies and results of MD simulations suggest that NH3 and H2O pass through the three monomeric urea channels in UT-B.

Office of Naval Research N00014-09-1-0246

Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP No. 08/128663)

Office of Naval Research Grant N00014-11-1-0889

NIH grant DK81567

National Institute of General Medical Sciences Grants R01-GM-086749

National Institute of General Medical Sciences R01-GM-101048

National Institute of General Medical Sciences U54-GM-087519

National Institute of General Medical Sciences P41-GM-104601

XSEDE (Grant No. MCA06N060)

Identificador

American Journal of Physiology Renal Physiology, Bethesda, v.304, n.12, p.F1447-F1457, 2013

http://www.producao.usp.br/handle/BDPI/44323

10.1152/ajprenal.00609.2012

http://dx.doi.org/10.1152/ajprenal.00609.2012

Idioma(s)

eng

Publicador

American Physiological Society

Bethesda

Relação

American Journal of Physiology Renal Physiology

Direitos

restrictedAccess

The American Physiological Society

Palavras-Chave #Carbon dioxide transport #Ammonia transport #Water transport #Urea transport #Membrane protein #Dióxido de carbono #Amônia #Uréia #Transporte através da membrana
Tipo

article

original article

publishedVersion