Abstract
Measurement of multiple fluorescence decay times of 1,6-diphenyl-1,3,5-hexatriene (DPH) in membranes can in principle be used to investigate structural domains of lipid bilayers. To assess the feasibility of this approach using phase and modulation techniques, we reduced experimental errors specifically associated with performing these measurements on membrane suspensions (probe self-quenching, background fluorescence, turbidity-induced artifacts) and determined empirically the level of precision thereby obtainable. Next we used these precision limits in theoretical calculations to conclude that the ratio of two coexisting decay times must exceed 1.3 if they are to be resolved with reliable accuracy. To demonstrate that such resolutions could be accomplished experimentally in membrane suspensions, three approaches were taken. First, the fluorescence decay of aqueous quinine sulfate quenched by chloride ion was resolved from that of membrane-associated DPH as long as the lifetime ratios of these two fluorophores exceeded the predicted value. Second, populations of DPH-containing lipid vesicles with single (or nearly single) decay times were mixed together, and when there were only two major lifetime components that differed by more than 30%, the resulting heterogeneous fluorescence could be resolved into the two expected lifetime components. Finally, DPH fluorescence decay measurements were correlated with phase behavior in well-characterized lipid systems, revealing a short lifetime component of DPH fluorescence associated with gel-phase lipid vesicles. From these studies, we conclude that only in special cases can co-existing gel and fluid phases be resolved by means of DPH lifetime heterogeneity, within the limits of precision defined herein.
Full text
PDF













Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andrich M. P., Vanderkooi J. M. Temperature dependence of 1,6-diphenyl-1,3,5-hexatriene fluorescence in phophoslipid artificial membranes. Biochemistry. 1976 Mar 23;15(6):1257–1261. doi: 10.1021/bi00651a013. [DOI] [PubMed] [Google Scholar]
- Barrow D. A., Lentz B. R. A model for the effect of lipid oxidation on diphenylhexatriene fluorescence in phospholipid vesicles. Biochim Biophys Acta. 1981 Jul 6;645(1):17–23. doi: 10.1016/0005-2736(81)90506-x. [DOI] [PubMed] [Google Scholar]
- Barrow D. A., Lentz B. R. Large vesicle contamination in small, unilamellar vesicles. Biochim Biophys Acta. 1980 Mar 27;597(1):92–99. doi: 10.1016/0005-2736(80)90153-4. [DOI] [PubMed] [Google Scholar]
- Barrow D. A., Lentz B. R. The use of isochronal reference standards in phase and modulation fluorescence lifetime measurements. J Biochem Biophys Methods. 1983 May;7(3):217–234. doi: 10.1016/0165-022x(83)90031-3. [DOI] [PubMed] [Google Scholar]
- Chen L. A., Dale R. E., Roth S., Brand L. Nanosecond time-dependent fluorescence depolarization of diphenylhexatriene in dimyristoyllecithin vesicles and the determination of "microviscosity". J Biol Chem. 1977 Apr 10;252(7):2163–2169. [PubMed] [Google Scholar]
- Dale R. E., Chen L. A., Brand L. Rotational relaxation of the "microviscosity" probe diphenylhexatriene in paraffin oil and egg lecithin vesicles. J Biol Chem. 1977 Nov 10;252(21):7500–7510. [PubMed] [Google Scholar]
- Gratton E., Limkeman M. A continuously variable frequency cross-correlation phase fluorometer with picosecond resolution. Biophys J. 1983 Dec;44(3):315–324. doi: 10.1016/S0006-3495(83)84305-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobson K., Papahadjopoulos D. Effect of a phase transition on the binding of 1-anilino-8-naphthalenesulfonate to phospholipid membranes. Biophys J. 1976 Jun;16(6):549–560. doi: 10.1016/S0006-3495(76)85710-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jähnig F. Structural order of lipids and proteins in membranes: evaluation of fluorescence anisotropy data. Proc Natl Acad Sci U S A. 1979 Dec;76(12):6361–6365. doi: 10.1073/pnas.76.12.6361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Karnovsky M. J., Kleinfeld A. M., Hoover R. L., Dawidowicz E. A., McIntyre D. E., Salzman E. A., Klausner R. D. Lipid domains in membranes. Ann N Y Acad Sci. 1982;401:61–75. doi: 10.1111/j.1749-6632.1982.tb25707.x. [DOI] [PubMed] [Google Scholar]
- Karnovsky M. J., Kleinfeld A. M., Hoover R. L., Klausner R. D. The concept of lipid domains in membranes. J Cell Biol. 1982 Jul;94(1):1–6. doi: 10.1083/jcb.94.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kawato S., Kinosita K., Jr, Ikegami A. Dynamic structure of lipid bilayers studied by nanosecond fluorescence techniques. Biochemistry. 1977 May 31;16(11):2319–2324. doi: 10.1021/bi00630a002. [DOI] [PubMed] [Google Scholar]
- Klausner R. D., Kleinfeld A. M., Hoover R. L., Karnovsky M. J. Lipid domains in membranes. Evidence derived from structural perturbations induced by free fatty acids and lifetime heterogeneity analysis. J Biol Chem. 1980 Feb 25;255(4):1286–1295. [PubMed] [Google Scholar]
- Lakowicz J. R., Cherek H., Balter A. Correction of timing errors in photomultiplier tubes used in phase-modulation fluorometry. J Biochem Biophys Methods. 1981 Sep;5(3):131–146. doi: 10.1016/0165-022x(81)90012-9. [DOI] [PubMed] [Google Scholar]
- Lentz B. R., Barenholz Y., Thompson T. E. Fluorescence depolarization studies of phase transitions and fluidity in phospholipid bilayers. 2 Two-component phosphatidylcholine liposomes. Biochemistry. 1976 Oct 5;15(20):4529–4537. doi: 10.1021/bi00665a030. [DOI] [PubMed] [Google Scholar]
- Lentz B. R., Barrow D. A., Hoechli M. Cholesterol-phosphatidylcholine interactions in multilamellar vesicles. Biochemistry. 1980 Apr 29;19(9):1943–1954. doi: 10.1021/bi00550a034. [DOI] [PubMed] [Google Scholar]
- Lentz B. R., Clubb K. W., Barrow D. A., Meissner G. Ordered and disordered phospholipid domains coexist in membranes containing the calcium pump protein of sarcoplasmic reticulum. Proc Natl Acad Sci U S A. 1983 May;80(10):2917–2921. doi: 10.1073/pnas.80.10.2917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lentz B. R., Freire E., Biltonen R. L. Fluorescence and calorimetric studies of phase transitions in phosphatidylcholine multilayers: kinetics of the pretransition. Biochemistry. 1978 Oct 17;17(21):4475–4480. doi: 10.1021/bi00614a018. [DOI] [PubMed] [Google Scholar]
- Mimms L. T., Zampighi G., Nozaki Y., Tanford C., Reynolds J. A. Phospholipid vesicle formation and transmembrane protein incorporation using octyl glucoside. Biochemistry. 1981 Feb 17;20(4):833–840. doi: 10.1021/bi00507a028. [DOI] [PubMed] [Google Scholar]
- Noordam P. C., Killian A., Oude Elferink R. F., De Gier J. Comparative study on the properties of saturated phosphatidylethanolamine and phosphatidylcholine bilayers: barrier characteristics and susceptibility to phospholipase A2 degradation. Chem Phys Lipids. 1982 Oct;31(2):191–204. doi: 10.1016/0009-3084(82)90044-5. [DOI] [PubMed] [Google Scholar]
- Parasassi T., Conti F., Glaser M., Gratton E. Detection of phospholipid phase separation. A multifrequency phase fluorimetry study of 1,6-diphenyl-1,3,5-hexatriene fluorescence. J Biol Chem. 1984 Nov 25;259(22):14011–14017. [PubMed] [Google Scholar]
- Parente R. A., Lentz B. R. Phase behavior of large unilamellar vesicles composed of synthetic phospholipids. Biochemistry. 1984 May 22;23(11):2353–2362. doi: 10.1021/bi00306a005. [DOI] [PubMed] [Google Scholar]
- Shinitzky M., Barenholz Y. Fluidity parameters of lipid regions determined by fluorescence polarization. Biochim Biophys Acta. 1978 Dec 15;515(4):367–394. doi: 10.1016/0304-4157(78)90010-2. [DOI] [PubMed] [Google Scholar]
- Stubbs C. D., Kouyama T., Kinosita K., Jr, Ikegami A. Effect of double bonds on the dynamic properties of the hydrocarbon region of lecithin bilayers. Biochemistry. 1981 Jul 21;20(15):4257–4262. doi: 10.1021/bi00518a004. [DOI] [PubMed] [Google Scholar]
- Suurkuusk J., Lentz B. R., Barenholz Y., Biltonen R. L., Thompson T. E. A calorimetric and fluorescent probe study of the gel-liquid crystalline phase transition in small, single-lamellar dipalmitoylphosphatidylcholine vesicles. Biochemistry. 1976 Apr 6;15(7):1393–1401. doi: 10.1021/bi00652a007. [DOI] [PubMed] [Google Scholar]
- Szoka F., Olson F., Heath T., Vail W., Mayhew E., Papahadjopoulos D. Preparation of unilamellar liposomes of intermediate size (0.1-0.2 mumol) by a combination of reverse phase evaporation and extrusion through polycarbonate membranes. Biochim Biophys Acta. 1980 Oct 2;601(3):559–571. doi: 10.1016/0005-2736(80)90558-1. [DOI] [PubMed] [Google Scholar]
- Wong M., Anthony F. H., Tillack T. W., Thompson T. E. Fusion of dipalmitoylphosphatidylcholine vesicles at 4 degrees C. Biochemistry. 1982 Aug 17;21(17):4126–4132. doi: 10.1021/bi00260a032. [DOI] [PubMed] [Google Scholar]
