PMID- 19879980 OWN - NLM STAT- MEDLINE DCOM- 20100401 LR - 20211020 IS - 0006-3002 (Print) IS - 0006-3002 (Linking) VI - 1804 IP - 2 DP - 2010 Feb TI - Evaluating the role of carbonic anhydrases in the transport of HCO3--related species. PG - 410-21 LID - 10.1016/j.bbapap.2009.10.021 [doi] AB - The soluble enzyme carbonic anhydrase II (CAII) plays an important role in CO(2) influx and efflux by red blood cells (RBCs), a process initiated by changes in the extracellular [CO(2)] (CO(2)-initiated CO(2) transport). Evidence suggests that CAII may be part of a macromolecular complex at the inner surface of the RBC membrane. Some have suggested CAII specifically binds to a motif on the cytoplasmic C terminus (Ct) of the Cl-HCO(3) exchanger AE1 and some other members of the SLC4 family of HCO(3)(-) transporters, a transport metabolon. Moreover, others have suggested that this bound CAII enhances the transport of HCO(3)(-)-related species-HCO(3)(-), CO(3)(), or CO(3)() ion pairs-when the process is initiated by altering the activity of the transporter (HCO(3)(-)-initiated HCO(3)(-) transport). In this review, I assess the theoretical roles of CAs in the transport of CO(2) and HCO(3)(-)-related species, concluding that although the effect of bound CAII on CO(2)-initiated CO(2) transport is expected to be substantial, the effect of bound CAs on HCO(3)(-)-initiated HCO(3)(-) transport is expected to be modest at best. I also assess the experimental evidence for CAII binding to AE1 and other transporters, and the effects of this binding on HCO(3)(-)-initiated HCO(3)(-) transport. The early conclusion that CAII binds to the Ct of AE1 appears to be the result of unpredictable effects of GST in the GST fusion proteins used in the studies. The early conclusion that bound CAII speeds HCO(3)(-)-initiated HCO(3)(-) transport appears to be the result of CAII accelerating the pH changes used as a read-out of transport. Thus, it appears that CAII does not bind directly to AE1 or other SLC4 proteins, and that bound CAII does not substantially accelerate HCO(3)(-)-initiated HCO(3)(-) transport. CI - Copyright 2009. Published by Elsevier B.V. FAU - Boron, Walter F AU - Boron WF AD - Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106-4970, USA. walter.boron@case.edu LA - eng GR - R01 NS018400/NS/NINDS NIH HHS/United States GR - R01 DK030344/DK/NIDDK NIH HHS/United States GR - R01 DK081567/DK/NIDDK NIH HHS/United States GR - R37 DK030344/DK/NIDDK NIH HHS/United States GR - DK30344/DK/NIDDK NIH HHS/United States GR - R37 DK030344-28/DK/NIDDK NIH HHS/United States GR - R01 NS018400-20/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Review DEP - 20091030 PL - Netherlands TA - Biochim Biophys Acta JT - Biochimica et biophysica acta JID - 0217513 RN - 0 (Bicarbonates) RN - EC 4.2.1.1 (Carbonic Anhydrases) SB - IM MH - Animals MH - Bicarbonates/*metabolism MH - Biological Transport MH - Carbonic Anhydrases/*physiology MH - Erythrocytes/metabolism MH - Humans PMC - PMC4699190 MID - NIHMS604657 EDAT- 2009/11/03 06:00 MHDA- 2010/04/02 06:00 PMCR- 2016/01/04 CRDT- 2009/11/03 06:00 PHST- 2009/09/11 00:00 [received] PHST- 2009/10/23 00:00 [revised] PHST- 2009/10/23 00:00 [accepted] PHST- 2009/11/03 06:00 [entrez] PHST- 2009/11/03 06:00 [pubmed] PHST- 2010/04/02 06:00 [medline] PHST- 2016/01/04 00:00 [pmc-release] AID - S1570-9639(09)00310-0 [pii] AID - 10.1016/j.bbapap.2009.10.021 [doi] PST - ppublish SO - Biochim Biophys Acta. 2010 Feb;1804(2):410-21. doi: 10.1016/j.bbapap.2009.10.021. Epub 2009 Oct 30.