Ionophore

Carrier ionophores

An ionophore is a chemical species that reversibly binds ions.[1] Many ionophores are lipid-soluble entities that transport ions across a cell membrane. Ionophore means "ion carrier" as these compounds catalyze ion transport across hydrophobic membranes such as liquid polymeric membranes (carrier-based ion selective electrodes) or lipid bilayers found in the living cells or synthetic vesicles (liposomes)[1]

Some ionophores are synthesized by microorganisms to import ions into their cells. Synthetic ion carriers have also been prepared. Ionophores selective for cations and anions have found many applications in analysis.[2]

The two broad classifications of ionophores synthesized by microorganisms are:

  1. Carrier ionophores that bind to a particular ion and shield its charge from the surrounding environment. This makes it easier for the ion to pass through the hydrophobic interior of the lipid membrane.[3] An example of a carrier ionophore is valinomycin, a molecule that transports a single potassium cation. Carrier ionophores may be proteins or other molecules.
  2. Channel formers that introduce a hydrophilic pore into the membrane, allowing ions to pass through without coming into contact with the membrane's hydrophobic interior.[4] An example of a channel former is gramicidin A. Channel forming ionophores are usually large proteins.

Mechanism of action of biologically relevant ionophores

The structure of the complex of sodium (Na+) and the antibiotic monensin A

Transmembrane ion concentration gradients (membrane potential) are required for living organisms. Ionophores can disrupt the membrane potential by conducting ions through a lipid membrane in the absence of a protein pore, and thus could exhibit cytotoxic properties. They are produced naturally by a variety of microbes and act as a defense against competing microbes.

Many antibiotics, particularly the macrolide antibiotics, are ionophores. Some exhibit high affinities for Na+, others high affinities for K+.[5] The structure of the sodium and potassium complexes of antibiotics have been verified by X-ray crystallography.[6]

Ionophores have been used to modify the permeability of biological membranes toward certain ions. Additionally, some ionophores are used as antibiotics and/or as growth-enhancing feed additives for certain animals, such as cattle (see monensin) and chickens.[7]

Synthetic ionophores

Structure of a potassium complex of a crown ether, a synthetic ionophore-ion complex

Many synthetic ionophores are based on crown ethers, cryptands, and calixarenes. These synthetic species are often macrocyclic.[5] Some synthetic agents are not macrocyclic, e.g., carbonyl cyanide-p-trifluoromethoxyphenylhydrazone. Even simple organic compounds, such as phenols, exhibit ionophoric properties. The majority of synthetic receptors used in the carrier-based anion-selective electrodes employ transition elements or metalloids as anion carriers, although simple organic urea- and thiourea based receptors are known.

List of representative biological ionophores

With the ion(s) they act upon:

Crystal structures have been determined for many of the alkali metal complexes formed by these compounds.[9]

See also

References

  1. 1 2 Bakker E1, Bühlmann P, Pretsch E. (1997). "Carrier-Based Ion-Selective Electrodes and Bulk Optodes. 1. General Characteristics". Chem Rev. 97 (8): 3083–3132. doi:10.1021/cr940394a.
  2. ↑ Bühlmann P1, Pretsch E, Bakker E. (1998). "Carrier-Based Ion-Selective Electrodes and Bulk Optodes. 2. Ionophores for Potentiometric and Optical Sensors". Chem Rev. 98 (4): 1593–1688. doi:10.1021/cr970113+.
  3. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "Ionophore".
  4. ↑ "Ionophores - MeSH Result".
  5. 1 2 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0-08-037941-9.
  6. ↑ Steinrauf, L. K.; Hamilton, J. A.; Sabesan, M. N. (1982). "Crystal structure of valinomycin-sodium picrate. Anion effects on valinomycin-cation complexes". Journal of the American Chemical Society 104 (15): 4085–4091. doi:10.1021/ja00379a008.
  7. ↑ Kabel, Marcus; Christine Simmons (2007-11-20). "USDA Revokes OK for Tyson Chicken Labels". Archived from the original on November 24, 2007. Retrieved 2007-11-20.
  8. ↑ Antonenko, YN; Yaguzhinsky, LS (18 February 1988). "The ion selectivity of nonelectrogenic ionophores measured on a bilayer lipid membrane: nigericin, monensin, A23187 and lasalocid A.". Biochimica et Biophysica Acta 938 (2): 125–30. doi:10.1016/0005-2736(88)90151-4. PMID 19927398.
  9. ↑ Katsuyuki, Aoki; Kazutaka, Murayama; Hu, Ning-Hai (2016). "Chapter 3, section 5. Naturally Occurring Antibiotic IOnophore Complexes". In Astrid, Sigel; Helmut, Sigel; Roland K.O., Sigel. The Alkali Metal Ions: Their Role in Life. Metal Ions in Life Sciences 16. Springer. pp. 74–92. doi:10.1007/978-3-319-21756-7_3.

External links

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