The subnanosecond fluorescence and motional dynamics of the tryptophan residue in the bacteriophage M13 coat protein incorporated within pure dioleoylphosphatidylcholine (DOPC) as well as dioleoylphosphatidylcholine/dioleoylphosphatidylglycerol (DOPC/DOPG) and dimyristoylphosphatidylcholine/dimyrist
Analysis of time-resolved fluorescence anisotropy in lipid-protein systems
โ Scribed by K. Peng; A. J. W. G. Visser; A. Hoek; C. J. A. M. Wolfs; J. C. Sanders; M. A. Hemminga
- Book ID
- 104656095
- Publisher
- Springer
- Year
- 1990
- Tongue
- English
- Weight
- 677 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1432-1017
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โฆ Synopsis
Fluorescent probes located in heterogeneous environments give rise to anomalous time-resolved fluorescence anisotropy. A simple analytical expression of anisotropy has been derived for the case of a small difference in local fluorescence lifetimes. The expression has the diagnostic advantage that the time dependence of the fluorescence anisotropy can be predicted from the differences in fluorescence lifetimes and residual anisotropies of the probes located in different sites. Using this model, the local fluorescence anisotropy parameters and the relative contributions of the lipid probe octadecyl rhodamine B in a lipid environment and in the vicinity of bacteriophage M13 coat protein reconstituted in phospholipid bilayers, composed of 80% 1,2-dimyristoyl-sn-glycero-3-phosphocholine and 20% 1,2-dimyristoyl-sn-glycero-3-phosphoglycerol have been determined experimentally. At 40 degrees C, the correlation times for bound and free probes are 2.3 and 3.0 ns, respectively, while the corresponding order parameters are 0.85 and 0.62, respectively.
๐ SIMILAR VOLUMES
Analysis of time-resolved fluorescence anisotropy measurements on DPH and TMA-DPH in POPC vesicles with and without cholesterol in terms of the rotational diffusion model shows two distinct x: minima which are statistically equivalent. This is explained by the fact that the anisotropy decay function