Relative CO₂/NH₃ selectivities of AQP1, AQP4, AQP5, AmtB, and RhAG

The water channel aquaporin 1 (AQP1) and certain Rh-family members are permeable to CO₂ and NH₃. Here, we use changes in surface pH (pHS) to assess relative CO₂ vs. NH₃ permeability of Xenopus oocytes expressing members of the AQP or Rh family. Exposed to CO₂ or NH₃, AQP1 oocytes exhibit a greater m...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 106; no. 13; pp. 5406 - 5411
Main Authors Musa-Aziz, Raif, Chen, Li-Ming, Pelletier, Marc F, Boron, Walter F
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 31.03.2009
National Acad Sciences
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Summary:The water channel aquaporin 1 (AQP1) and certain Rh-family members are permeable to CO₂ and NH₃. Here, we use changes in surface pH (pHS) to assess relative CO₂ vs. NH₃ permeability of Xenopus oocytes expressing members of the AQP or Rh family. Exposed to CO₂ or NH₃, AQP1 oocytes exhibit a greater maximal magnitude of pHS change (ΔpHS) compared with day-matched controls injected with H₂O or with RNA encoding SGLT1, NKCC2, or PepT1. With CO₂, AQP1 oocytes also have faster time constants for pHS relaxation (τpHs). Thus, AQP1, but not the other proteins, conduct CO₂ and NH₃. Oocytes expressing rat AQP4, rat AQP5, human RhAG, or the bacterial Rh homolog AmtB also exhibit greater ΔpHS(CO₂) and faster τpHs compared with controls. Oocytes expressing AmtB and RhAG, but not AQP4 or AQP5, exhibit greater ΔpHS(NH₃) values. Only AQPs exhibited significant osmotic water permeability (Pf). We computed channel-dependent (*) ΔpHS or Pf by subtracting values for H₂O oocytes from those of channel-expressing oocytes. For the ratio ΔpHS(CO₂)*/P[Formula: see text]*, the sequence was AQP5 > AQP1 [congruent with] AQP4. For ΔpHS(CO₂)*/ΔpHS(NH₃)*, the sequence was AQP4 [congruent with] AQP5 > AQP1 > AmtB > RhAG. Thus, each channel exhibits a characteristic ratio for indices of CO₂ vs. NH₃ permeability, demonstrating that, like ion channels, gas channels can exhibit selectivity.
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2R.M.-A. and L.-M.C. contributed equally to this work.
Author contributions: R.M.-A., L.-M.C., M.F.P., and W.F.B. designed research; R.M.-A., L.-M.C., and M.F.P. performed research; R.M.-A. analyzed data; and R.M.-A., L.-M.C., and W.F.B. wrote the paper.
Communicated by Gerhard Giebisch, Yale University School of Medicine, New Haven, CT, December 30, 2008
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0813231106