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Quantitative visualization of passive transport across bilayer lipid membranes
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Grime, John M. A., Edwards, Martin A., Rudd, Nicola C. and Unwin, Patrick R.. (2008) Quantitative visualization of passive transport across bilayer lipid membranes. Proceedings of the National Academy of Sciences of the United States of America, Vol.105 (No.38). pp. 14277-14282. ISSN 0027-8424
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Official URL: http://dx.doi.org/10.1073/pnas.0803720105
Abstract
The ability to predict and interpret membrane permeation coefficients is of critical importance, particularly because passive transport is crucial for the effective delivery of many pharmaceutical agents to intracellular targets. We present a method for the quantitative measurement of the permeation coefficients of protonophores by using laser confocal scanning microscopy coupled to microelectrochemistry, which is amenable to precise modeling with the finite element method. The technique delivers well defined and high mass transport rates and allows rapid visualization of the entire pH distribution on both the cis and trans side of model bilayer lipid membranes (BLMs). A homologous series of carboxylic acids was investigated as probe molecules for BLMs composed of soybean phosphatidylcholine. Significantly, the permeation coefficient decreased with acyl tail length contrary to previous work and to Overton's rule. The reasons for this difference are considered, and we suggest that the applicability of Overton's rule requires re-evaluation.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QC Physics Q Science > QD Chemistry Q Science > QH Natural history > QH301 Biology |
| Divisions: | Faculty of Science > Chemistry |
| Library of Congress Subject Headings (LCSH): | Ultramicroelectrodes, Confocal microscopy, Finite element method, Bilayer lipid membranes, Biological transport |
| Journal or Publication Title: | Proceedings of the National Academy of Sciences of the United States of America |
| Publisher: | National Academy of Sciences |
| ISSN: | 0027-8424 |
| Date: | 23 September 2008 |
| Volume: | Vol.105 |
| Number: | No.38 |
| Number of Pages: | 6 |
| Page Range: | pp. 14277-14282 |
| Identification Number: | 10.1073/pnas.0803720105 |
| Status: | Not Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| Funder: | Engineering and Physical Sciences Research Council (EPSRC), University of Warwick |
| References: | 1. Krylov AV, Pohl P, Zeidel ML, Hill WG (2001) Water permeability of asymmetric planar lipid bilayers: Leaflets of different composition offer independent and additive resistances to permeation. J Gen Physiol 118:333–340. 2. Gennis RB (1989) Biomembranes (Springer, New York). 3. Doan KMM, et al. (2002) Passive permeability and P-glycoprotein-mediated efflux differentiate central nervous system (CNS) and non-CNS marketed drugs. J Pharmacol Exp Ther 303:1029–1037. 4. Doppenschmitt S, Spahn-Langguth H, Regardh CG, Langguth P (1999) Role of Pglycoprotein- mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein. J Pharm Sci 88:1067–1072. 5. Stein WD, Lieb WR (1986) Transport and Diffusion Across Cell Membranes (Academic, New York). 6. Cairns,D(2003) Essentials of Pharmaceutical Chemistry (Pharmaceutical Press, London) pp 57–69). 7. Gottlieb E, Armour SM, Harris MH, Thompson CB (2003) Mitochondrial membrane potential regulates matrix configuration and cytochrome c release during apoptosis. Nat Cell Death Differentiation 10:709–717. 8. Yamasaki H, et al. (1991) Induction of the H� release from thylakoid membranes by illumination in the presence of protonophores at high concentrations. Plant Cell Physiol 32:925–934. 9. Wolosin JM, Ginsburg H (1975) The permeation of organic acids through lecithin bilayers resemblance to diffusion in polymers. Biochim Biophys Acta 389:20–33. 10. Alger JR, Prestegard JH (1979) Nuclear magnetic resonance study of acetic acid permeation of large unilamellar vesicle membranes. Biophys J 28:1–14. 11. Walter A, Hastings D, Gutknecht J (1982) Weak acid permeability through lipid bilayer membranes. J Gen Physiol 79:917–933. 12. Walter A, Gutknecht J (1984) Monocarboxylic acid permeation through lipid bilayer membranes. J Membr Biol 77:255–264. 13. Walter A, Gutknecht J (1986) Permeability of small nonelectrolytes through lipid bilayer membranes. J Membr Biol 90:207–217. 14. Xiang T-X, Anderson BD (1995) Phospholipid surface density determines the partitioning and permeability of acetic acid in DMPC:cholesterol bilayers. JMembr Biol 148:157– 167. 15. Evtodienko VY, Kovbasnjuk ON, Antonenko YN, Yaguzhinsky LS (1996) Effect of the alkyl chain length of monocarboxylic acid on the permeation through bilayer lipid membranes. Biochim Biophys Acta 1281:245–251. 16. Xiang T-X, Anderson BD (1997) Permeability of acetic acid across gel and liquidcrystalline lipid bilayers conforms to free-surface-area theory. Biophys J 72:223–237. 17. Xiang T-X, Anderson BD (1998) Influence of chain ordering on the selectivity of dipalmitoylphosphatidylcholine bilayer membranes for permeant size and shape. Biophys J 75:2658–2671. 18. Overton CE (1899) On the general osmotic properties of the cell, their probable origin, and their significance for physiology. Vierteljahrsschr Naturforsch Ges Zurich 44:88– 135 (translated from German). 19. Overton CE (1901) Studies in Narcosis (Fischer, Jena, Germany) (translated from German). 20. Orbach E, Finkelstein A (1980) The nonelectrolyte permeability of planar lipid bilayer membranes. J Gen Physiol 75:427–436. 21. Saparov SM, Antonenko YN, Pohl P (2006) A new model of weak acid permeation through membranes revisited: Does Overton still rule? Biophys J 90:L86–L88. 22. Al-Awqati Q (1999) One hundred years of membrane permeability: Does Overton still rule? Nat Cell Biol 1:E201–E202. 23. Levin VA (1980) Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeability. J Med Chem 23:682–684. 24. Lin R-Y, Hsu C-W, Chen W-Y (1996) A method to predict the transdermal permeability of amino acids and dipeptides through porcine skin. J Controlled Release 38:229–234. 25. Camenisch G, Alsenz J, van de Waterbeemd H, Folkers G (1998) Estimation of permeability by passive diffusion through Caco-2 cell monolayers using the drugs lipophilicity and molecular weight. Eur J Pharm Sci 6:313–319. 26. Edwards A, Prausnitz MR (2001) Predicted permeability of the cornea to topical drugs. Pharm Res 18:1497–1508. 27. Pohl P, Saparov SM, Antonenko YN (1997) The effect of a transmembrane osmotic flux on the ion concentration distribution in the immediate membrane vicinity measured by microelectrodes. Biophys J 72:1711–1718. 28. Antonenko YN, Bulychev AA (1991) Measurements of local pH changes near bilayer lipid membrane by means of a pH microelectrode and a protonophore-dependent membrane potential: Comparison of the methods. Biochim Biophys Acta 1070:279– 282. 29. Antonenko YN, Pohl P (1995) Steady-state nonmonotonic concentration profiles of bilayer lipid membranes in the unstirred layers. Biochim Biophys Acta 1235:57–61. 30. Pohl P, Saparov SM, Antonenko YN (1998) The size of the unstirred layer as a function of the solute diffusion coefficient. Biophys J 75:1403–1409. 31. Tsionsky M, Zhou J, Amemiya S, Fan F-RF, Bard AJ (1999) Scanning electrochemical microscopy. 38. Application of SECM to the study of charge transfer through bilayer lipid membranes. Anal Chem 71:4300–4305. 32. Mauzeroll J, Bard AJ (2004) Scanning electrochemical microscopy of menadioneglutathione conjugate export from yeast cells. Proc Natl Acad Sci USA 101:7862–7867. 33. Yamada H, Matsue T, Uchida I (1991) A microvoltammetric study of permeation of ferrocene derivatives through planar bilayer lipid membrane. Biochim Biophys Acta 180:1330–1334. 34. Matsue T, Shiku H, Yamada H, Uchida I (1994) Permselectivity of voltage-gated ion channel studied by microamperometry. J Phys Chem 98:11001–11003. 35. Gonsalves M, et al. (2000) Scanning electrochemical microscopy as a local probe of oxygen permeability in cartilage. Biophys J 78:1578–1588. 36. Scott ER, White HS (1991) Scanning electrochemical microscopy of a porous membrane. J Membr Sci 58:71–87. 37. Rudd NC, et al. (2005) Fluorescence confocal laser scanning microscopy as a probe of pH gradients in electrode reactions and surface activity. Anal Chem 77:6205–6217. 38. Davies CW (1989) An Introduction to Splines for Use in Computer Graphics and Geometric Modeling (Morgan Kaufmann, San Francisco, CA) pp 211–245. 39. Miller DM (1991) Evidence that interfacial transport is rate-limiting during passive cell membrane permeation. Biochim Biophys Acta 1065:75–81. 40. O’Neill SD, Leopold AC (1982) An assessment of phase transitions in soybean membranes. Plant Physiol 70:1405–1409. 41. Wightman RM, Wipf DO (1989) Electroanalytical Chemistry, ed Bard AJ (Dekker, New York), Vol 15, pp 329–333. 42. Mueller P, Rudin DO, Tien HT, Wescott WC (1963) Methods for the formation of single bimolecular lipid membranes in aqueous solution. J Phys Chem 67:534–535. 43. Tien HT (1974) Bilayer Lipid Membranes (BLM): Theory and Practice (Dekker, New York). 44. Edwards MA, Martin S, Whitworth AL, Macpherson JV, Unwin PR (2006) Scanning electrochemical microscopy: Principles and applications to biophysical systems. Physiol Measurements 27:R63–R108. 45. Davies CW (1962) Ion Association (Butterworths, London) p 47. |
| URI: | http://wrap.warwick.ac.uk/id/eprint/29289 |
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