Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1979 Oct 5;50(1):23-41.
doi: 10.1007/BF01868786.

HCO3-/Cl- exchange across the human erythrocyte membrane: effects of pH and temperature

HCO3-/Cl- exchange across the human erythrocyte membrane: effects of pH and temperature

A L Obaid et al. J Membr Biol. .

Abstract

Changes in extracellular pH (PH0) in red cell suspensions were monitored in a stopped-flow rapid reaction apparatus under conditions where dpH0/dt was determined by the rate of HCO3-/Cl- exchange across the membrane. Experiments were performed at 5 degrees C less than T less than 40 degrees C using either untreated cells or cells exposed to 0.11 mM SITS (4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonic acid). Although SITS exposure reduced the rate of exchange by 90%, both untreated and SITS-treated cells are similarly affected by changes in pH0 and temperature. The rate of HCO3-/Cl- exchange exhibits a minimum at about pH0 5 and a maximum at about pH0 7.4 at all temperatures. A transition temperature of 17 degrees C was observed in the Arrhenius relationship for all pH0. The activation energies (Ea) in kcal/mol are 19.6 below and 11.7 above 17 degrees C for 5 less than pH0 less than 8. These findings, similar to those reported for Cl- self-exchange, suggest that: (i) a change in the rate-limiting step for HCO3-/Cl- exchange occurs at 17 degrees C, possibly due to an altered interaction between the transport pathway and membrane lipids; (ii) the carrier system can be titrated by either H+ or SITS from the outside of the membrane, but the untitrated sites continue to transport normally; (iii) the pH0 dependence of the rate of exchange is consistent with the titratable carrier having its most alkaline pK in the range expected for amino groups; and (iv) below pH0 5, the nature of the exchange is markedly altered.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Fed Proc. 1976 Jan;35(1):3-10 - PubMed
    1. Q Rev Biophys. 1975 May;8(2):185-235 - PubMed
    1. J Physiol. 1962 Mar;160:392-403 - PubMed
    1. J Membr Biol. 1977 Jan 28;30(4):319-50 - PubMed
    1. J Cell Physiol. 1975 Dec;86(3 Pt 1):471-94 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources