Literature DB >> 3651418

Fluorescence lifetime distributions of 1,6-diphenyl-1,3,5-hexatriene in phospholipid vesicles.

R Fiorini1, M Valentino, S Wang, M Glaser, E Gratton.   

Abstract

The fluorescence emission properties of 1,6-diphenyl-1,3,5-hexatriene (DPH) in 1,2-dipalmitoyl-3-sn-phosphatidylcholine and 1,2-dimyristoyl-3-sn-phosphatidylcholine multilamellar vesicles have been measured by using multifrequency phase fluorometry. The fluorescence decay of DPH in the phospholipid vesicles has been analyzed by assuming either that the decay is made up of a discrete sum of exponential components or that the decay is made up of one or more continuous distributions of lifetime components. The fit of the decay curve using exponentials required at least two terms, and the reduced X2 was relatively large. The fit using a continuous distribution of lifetime values used two continuous components. Several symmetric distribution functions were used: uniform, Gaussian, and Lorentzian. The distribution function that best described the decay was the Lorentzian. The full width at half-maximum of the Lorentzian distribution was about 0.6 ns at temperatures below the phase transition temperature. At the phospholipid phase transition and at higher temperatures, the distribution became quite narrow, with a width of about 0.1 ns. It is proposed that the lifetime distribution is generated by a continuum of different environments of the DPH molecule characterized by different dielectric constants. Below the transition temperature in the gel phase, the dielectric constant gradient along the membrane normal determines the distribution of decay rates. Above the transition, in the liquid-crystalline phase, the translational and rotational mobility of the DPH molecule increases, and the DPH experiences an average environment during the excited-state lifetime. Consequently, the distribution becomes narrower.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1987        PMID: 3651418     DOI: 10.1021/bi00387a019

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  20 in total

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2.  Applications of phasors to in vitro time-resolved fluorescence measurements.

Authors:  Martin Stefl; Nicholas G James; Justin A Ross; David M Jameson
Journal:  Anal Biochem       Date:  2010-11-13       Impact factor: 3.365

3.  Fluorescence lifetime distributions in membrane systems.

Authors:  E Gratton; T Parasassi
Journal:  J Fluoresc       Date:  1995-03       Impact factor: 2.217

4.  The carbohydrate moieties of the beta-subunit of Na+, K(+)-ATPase: their lateral motions and proximity to the cardiac glycoside site.

Authors:  E Amler; A Abbott; H Malak; J Lakowicz; W J Ball
Journal:  Biophys J       Date:  1996-01       Impact factor: 4.033

5.  Fluorescence lifetime distributions of diphenylhexatriene-labeled phosphatidylcholine as a tool for the study of phospholipid-cholesterol interactions.

Authors:  E Kalb; F Paltauf; A Hermetter
Journal:  Biophys J       Date:  1989-12       Impact factor: 4.033

6.  Molecular order and fluidity of the plasma membrane of human platelets from time-resolved fluorescence depolarization.

Authors:  C R Mateo; M P Lillo; J González-Rodríguez; A U Acuña
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7.  Hydration at the membrane protein-lipid interface.

Authors:  C Ho; C D Stubbs
Journal:  Biophys J       Date:  1992-10       Impact factor: 4.033

8.  Study of plasma membrane heterogeneity using a phosphatidylcholine derivative of 1,6-diphenyl-1,3,5-hexatriene [2-(3-(diphenylhexatriene)propanoyl)-3-palmitoyl-L-α-phosphatidylcholine].

Authors:  A Tangorra; G Ferretti; G Zolese; G Curatola
Journal:  J Fluoresc       Date:  1994-12       Impact factor: 2.217

9.  Properties of palmitoyl phosphatidylcholine, sphingomyelin, and dihydrosphingomyelin bilayer membranes as reported by different fluorescent reporter molecules.

Authors:  Thomas Nyholm; Matts Nylund; Annu Söderholm; J Peter Slotte
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

10.  Dexamethasone modulates rat renal brush border membrane phosphate transporter mRNA and protein abundance and glycosphingolipid composition.

Authors:  M Levi; J A Shayman; A Abe; S K Gross; R H McCluer; J Biber; H Murer; M Lötscher; R E Cronin
Journal:  J Clin Invest       Date:  1995-07       Impact factor: 14.808

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