Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1998 Jul;75(1):342–353. doi: 10.1016/S0006-3495(98)77518-6

Submicron structure in L-alpha-dipalmitoylphosphatidylcholine monolayers and bilayers probed with confocal, atomic force, and near-field microscopy.

C W Hollars 1, R C Dunn 1
PMCID: PMC1299703  PMID: 9649391

Abstract

Langmuir-Blodgett (LB) monolayers and bilayers of L-alpha-dipalmitoylphosphatidylcholine (DPPC), fluorescently doped with 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (diIC18), are studied by confocal microscopy, atomic force microscopy (AFM), and near-field scanning optical microscopy (NSOM). Beyond the resolution limit of confocal microscopy, both AFM and NSOM measurements of mica-supported lipid monolayers reveal small domains on the submicron scale. In the NSOM studies, simultaneous high-resolution fluorescence and topography measurements of these structures confirm that they arise from coexisting liquid condensed (LC) and liquid expanded (LE) lipid phases, and not defects in the monolayer. AFM studies of bilayers formed by a combination of LB dipping and Langmuir-Schaefer monolayer transfer exhibit complex surface topographies that reflect a convolution of the phase structure present in each of the individual monolayers. NSOM fluorescence measurements, however, are able to resolve the underlying lipid domains from each side of the bilayer and show that they are qualitatively similar to those observed in the monolayers. The observation of the small lipid domains in these bilayers is beyond the spatial resolving power of confocal microscopy and is complicated in the topography measurements taken with AFM, illustrating the utility of NSOM for these types of studies. The data suggest that the small LC and LE lipid domains are formed after lipid transfer to the substrate through a dewetting mechanism. The possible extension of these measurements to probing for lipid phase domains in natural biomembranes is discussed.

Full Text

The Full Text of this article is available as a PDF (398.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ambrose W. P., Goodwin P. M., Keller R. A., Martin J. C. Alterations of single molecule fluorescence lifetimes in near-field optical microscopy. Science. 1994 Jul 15;265(5170):364–367. doi: 10.1126/science.265.5170.364. [DOI] [PubMed] [Google Scholar]
  2. Baeza I., Wong C., Mondragón R., González S., Ibáez M., Farfán N., Argüello C. Transbilayer diffusion of divalent cations into liposomes mediated by lipidic particles of phosphatidate. J Mol Evol. 1994 Dec;39(6):560–568. doi: 10.1007/BF00160401. [DOI] [PubMed] [Google Scholar]
  3. Baldwin P. A., Hubbell W. L. Effects of lipid environment on the light-induced conformational changes of rhodopsin. 2. Roles of lipid chain length, unsaturation, and phase state. Biochemistry. 1985 May 21;24(11):2633–2639. doi: 10.1021/bi00332a007. [DOI] [PubMed] [Google Scholar]
  4. Betzig E., Chichester R. J. Single molecules observed by near-field scanning optical microscopy. Science. 1993 Nov 26;262(5138):1422–1425. doi: 10.1126/science.262.5138.1422. [DOI] [PubMed] [Google Scholar]
  5. Betzig E., Trautman J. K., Harris T. D., Weiner J. S., Kostelak R. L. Breaking the diffraction barrier: optical microscopy on a nanometric scale. Science. 1991 Mar 22;251(5000):1468–1470. doi: 10.1126/science.251.5000.1468. [DOI] [PubMed] [Google Scholar]
  6. Bourdieu L., Ronsin O., Chatenay D. Molecular positional order in langmuir-blodgett films by atomic force microscopy. Science. 1993 Feb 5;259(5096):798–801. doi: 10.1126/science.259.5096.798. [DOI] [PubMed] [Google Scholar]
  7. Caffrey M., Feigenson G. W. Fluorescence quenching in model membranes. 3. Relationship between calcium adenosinetriphosphatase enzyme activity and the affinity of the protein for phosphatidylcholines with different acyl chain characteristics. Biochemistry. 1981 Mar 31;20(7):1949–1961. doi: 10.1021/bi00510a034. [DOI] [PubMed] [Google Scholar]
  8. Chernomordik L. V., Zimmerberg J. Bending membranes to the task: structural intermediates in bilayer fusion. Curr Opin Struct Biol. 1995 Aug;5(4):541–547. doi: 10.1016/0959-440x(95)80041-7. [DOI] [PubMed] [Google Scholar]
  9. Chi L. F., Anders M., Fuchs H., Johnston R. R., Ringsdorf H. Domain structures in langmuir-blodgett films investigated by atomic force microscopy. Science. 1993 Jan 8;259(5092):213–216. doi: 10.1126/science.259.5092.213. [DOI] [PubMed] [Google Scholar]
  10. Criado M., Eibl H., Barrantes F. J. Functional properties of the acetylcholine receptor incorporated in model lipid membranes. Differential effects of chain length and head group of phospholipids on receptor affinity states and receptor-mediated ion translocation. J Biol Chem. 1984 Jul 25;259(14):9188–9198. [PubMed] [Google Scholar]
  11. Derzko Z., Jacobson K. Comparative lateral diffusion of fluorescent lipid analogues in phospholipid multibilayers. Biochemistry. 1980 Dec 23;19(26):6050–6057. doi: 10.1021/bi00567a016. [DOI] [PubMed] [Google Scholar]
  12. Dupou L., Lopez A., Tocanne J. F. Comparative study of the lateral motion of extrinsic probes and anthracene-labelled constitutive phospholipids in the plasma membrane of Chinese hamster ovary cells. Eur J Biochem. 1988 Feb 1;171(3):669–674. doi: 10.1111/j.1432-1033.1988.tb13838.x. [DOI] [PubMed] [Google Scholar]
  13. Enderle T., Ha T., Ogletree D. F., Chemla D. S., Magowan C., Weiss S. Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy. Proc Natl Acad Sci U S A. 1997 Jan 21;94(2):520–525. doi: 10.1073/pnas.94.2.520. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Epand R. M., Epand R. F. Calorimetric detection of curvature strain in phospholipid bilayers. Biophys J. 1994 May;66(5):1450–1456. doi: 10.1016/S0006-3495(94)80935-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Fang Y., Yang J. The growth of bilayer defects and the induction of interdigitated domains in the lipid-loss process of supported phospholipid bilayers. Biochim Biophys Acta. 1997 Mar 13;1324(2):309–319. doi: 10.1016/s0005-2736(96)00236-2. [DOI] [PubMed] [Google Scholar]
  16. Furtula V., Khan I. A., Nothnagel E. A. Selective osmotic effect on diffusion of plasma membrane lipids in maize protoplasts. Proc Natl Acad Sci U S A. 1990 Sep;87(17):6532–6536. doi: 10.1073/pnas.87.17.6532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gibson N. J., Brown M. F. Lipid headgroup and acyl chain composition modulate the MI-MII equilibrium of rhodopsin in recombinant membranes. Biochemistry. 1993 Mar 9;32(9):2438–2454. doi: 10.1021/bi00060a040. [DOI] [PubMed] [Google Scholar]
  18. Ha T., Enderle T., Ogletree D. F., Chemla D. S., Selvin P. R., Weiss S. Probing the interaction between two single molecules: fluorescence resonance energy transfer between a single donor and a single acceptor. Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6264–6268. doi: 10.1073/pnas.93.13.6264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hui S. W., Sen A. Effects of lipid packing on polymorphic phase behavior and membrane properties. Proc Natl Acad Sci U S A. 1989 Aug;86(15):5825–5829. doi: 10.1073/pnas.86.15.5825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Hwang J., Tamm L. K., Böhm, Ramalingam T. S., Betzig E., Edidin M. Nanoscale complexity of phospholipid monolayers investigated by near-field scanning optical microscopy. Science. 1995 Oct 27;270(5236):610–614. doi: 10.1126/science.270.5236.610. [DOI] [PubMed] [Google Scholar]
  21. Johannsson A., Smith G. A., Metcalfe J. C. The effect of bilayer thickness on the activity of (Na+ + K+)-ATPase. Biochim Biophys Acta. 1981 Mar 6;641(2):416–421. doi: 10.1016/0005-2736(81)90498-3. [DOI] [PubMed] [Google Scholar]
  22. Johnson M., Edidin M. Lateral diffusion in plasma membrane of mouse egg is restricted after fertilisation. Nature. 1978 Mar 30;272(5652):448–450. doi: 10.1038/272448a0. [DOI] [PubMed] [Google Scholar]
  23. Kelusky E. C., Smith I. C. Characterization of the binding of the local anesthetics procaine and tetracaine to model membranes of phosphatidylethanolamine: a deuterium nuclear magnetic resonance study. Biochemistry. 1983 Dec 6;22(25):6011–6017. doi: 10.1021/bi00294a049. [DOI] [PubMed] [Google Scholar]
  24. Knapp H. F., Wiegräbe W., Heim M., Eschrich R., Guckenberger R. Atomic force microscope measurements and manipulation of Langmuir-Blodgett films with modified tips. Biophys J. 1995 Aug;69(2):708–715. doi: 10.1016/S0006-3495(95)79946-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Knobler C. M. Seeing phenomena in flatland: studies of monolayers by fluorescence microscopy. Science. 1990 Aug 24;249(4971):870–874. doi: 10.1126/science.249.4971.870. [DOI] [PubMed] [Google Scholar]
  26. Lehtonen J. Y., Kinnunen P. K. Poly(ethylene glycol)-induced and temperature-dependent phase separation in fluid binary phospholipid membranes. Biophys J. 1995 Feb;68(2):525–535. doi: 10.1016/S0006-3495(95)80214-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Lundbaek J. A., Birn P., Girshman J., Hansen A. J., Andersen O. S. Membrane stiffness and channel function. Biochemistry. 1996 Mar 26;35(12):3825–3830. doi: 10.1021/bi952250b. [DOI] [PubMed] [Google Scholar]
  28. McCallum C. D., Epand R. M. Insulin receptor autophosphorylation and signaling is altered by modulation of membrane physical properties. Biochemistry. 1995 Feb 14;34(6):1815–1824. doi: 10.1021/bi00006a001. [DOI] [PubMed] [Google Scholar]
  29. McConnell H. M., Tamm L. K., Weis R. M. Periodic structures in lipid monolayer phase transitions. Proc Natl Acad Sci U S A. 1984 May;81(10):3249–3253. doi: 10.1073/pnas.81.10.3249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Metcalf T. N., Wang J. L., Schindler M. Lateral diffusion of phospholipids in the plasma membrane of soybean protoplasts: Evidence for membrane lipid domains. Proc Natl Acad Sci U S A. 1986 Jan;83(1):95–99. doi: 10.1073/pnas.83.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Mikrut JM, Dutta P, Ketterson JB, MacDonald RC. Atomic-force and fluorescence microscopy of Langmuir-Blodgett monolayers of L- alpha -dimyristoylphosphatidic acid. Phys Rev B Condens Matter. 1993 Nov 15;48(19):14479–14487. doi: 10.1103/physrevb.48.14479. [DOI] [PubMed] [Google Scholar]
  32. Möhwald H. Phospholipid and phospholipid-protein monolayers at the air/water interface. Annu Rev Phys Chem. 1990;41:441–476. doi: 10.1146/annurev.pc.41.100190.002301. [DOI] [PubMed] [Google Scholar]
  33. Navarro J., Toivio-Kinnucan M., Racker E. Effect of lipid composition on the calcium/adenosine 5'-triphosphate coupling ratio of the Ca2+-ATPase of sarcoplasmic reticulum. Biochemistry. 1984 Jan 3;23(1):130–135. doi: 10.1021/bi00296a021. [DOI] [PubMed] [Google Scholar]
  34. Petersen N. O., McConnaughey W. B. Effects of multiple membranes on measurements of cell surface dynamics by fluorescence photobleaching. J Supramol Struct Cell Biochem. 1981;17(3):213–221. doi: 10.1002/jsscb.380170303. [DOI] [PubMed] [Google Scholar]
  35. Reiter G. Dewetting of thin polymer films. Phys Rev Lett. 1992 Jan 6;68(1):75–78. doi: 10.1103/PhysRevLett.68.75. [DOI] [PubMed] [Google Scholar]
  36. Riegler JE, LeGrange JD. Observation of a monolayer phase transition on the meniscus in a Langmuir-Blodgett transfer configuration. Phys Rev Lett. 1988 Nov 21;61(21):2492–2495. doi: 10.1103/PhysRevLett.61.2492. [DOI] [PubMed] [Google Scholar]
  37. Rilfors L., Hauksson J. B., Lindblom G. Regulation and phase equilibria of membrane lipids from Bacillus megaterium and Acholeplasma laidlawii strain A containing methyl-branched acyl chains. Biochemistry. 1994 May 24;33(20):6110–6120. doi: 10.1021/bi00186a010. [DOI] [PubMed] [Google Scholar]
  38. Sackmann E. Supported membranes: scientific and practical applications. Science. 1996 Jan 5;271(5245):43–48. doi: 10.1126/science.271.5245.43. [DOI] [PubMed] [Google Scholar]
  39. Sackmann E. The seventh Datta Lecture. Membrane bending energy concept of vesicle- and cell-shapes and shape-transitions. FEBS Lett. 1994 Jun 6;346(1):3–16. doi: 10.1016/0014-5793(94)00484-6. [DOI] [PubMed] [Google Scholar]
  40. Salamon Z., Wang Y., Brown M. F., Macleod H. A., Tollin G. Conformational changes in rhodopsin probed by surface plasmon resonance spectroscopy. Biochemistry. 1994 Nov 22;33(46):13706–13711. doi: 10.1021/bi00250a022. [DOI] [PubMed] [Google Scholar]
  41. Tocanne J. F., Dupou-Cézanne L., Lopez A. Lateral diffusion of lipids in model and natural membranes. Prog Lipid Res. 1994;33(3):203–237. doi: 10.1016/0163-7827(94)90027-2. [DOI] [PubMed] [Google Scholar]
  42. Tollner K, Popovitz-Biro R, Lahav M, Milstein D. Impact of molecular order in langmuir-blodgett films on catalysis . Science. 1997 Dec 19;278(5346):2100–2102. doi: 10.1126/science.278.5346.2100. [DOI] [PubMed] [Google Scholar]
  43. Wolf D. E., Lipscomb A. C., Maynard V. M. Causes of nondiffusing lipid in the plasma membrane of mammalian spermatozoa. Biochemistry. 1988 Feb 9;27(3):860–865. doi: 10.1021/bi00403a004. [DOI] [PubMed] [Google Scholar]
  44. Xie X. S., Dunn R. C. Probing single molecule dynamics. Science. 1994 Jul 15;265(5170):361–364. doi: 10.1126/science.265.5170.361. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES