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
. 1977 Nov 15;168(2):289-97.
doi: 10.1042/bj1680289.

Passive ion permeability of the chromaffin-granule membrane

Passive ion permeability of the chromaffin-granule membrane

J H Phillips. Biochem J. .

Abstract

'Ghosts' of bovine chromaffin granules, in which the complex mixture of proteins and solutes normally found in the granule matrix is replaced by buffered sucrose are osmotically sensitive. They shrink when the osmotic pressure of the suspension medium is increased, and swell if solute entry is facilitated by the addition of ionophores. Swelling in the presence of ionophores has been used to investigate the passive ion permeability of these membranes. They have a very low permeability to K+ ions (of the order of 10(-10) cm/s); their permeability to protons, Na+ and choline ions is too low to be detected by these methods. Their passive permeability to anions decreases in the order: CNS- greater than I- greater than CCl3CO2- greater than Br- greater than Cl- greater than SO4(2)- greater than CH3CO2-, HCO3-, F-, PO4(3)- the permeability to hiocyanate being of the order of 10(-7) cm/s. Coupled proton and anion entry is extremely slow, except for weak acids. Fluoride, unexpectedly, also appears to enter rapidly when proton/K+ exchange is facilitated by nigericin. In the presence of K+ salts, nigericin, like valinomycin, induces lysis of intact granules, an effect that is not dependent on the presence of a permeant anion, but is dependent on the pH gradient across the membrane.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Gen Physiol. 1976 Dec;68(6):601-31 - PubMed
    1. Mol Pharmacol. 1975 Nov;11(6):745-50 - PubMed
    1. Neuroscience. 1976;1(5):399-412 - PubMed
    1. Biochem Pharmacol. 1976 May 1;25(9):1035-8 - PubMed
    1. Biochim Biophys Acta. 1958 May;28(2):392-402 - PubMed