Quantitative fluorescence spectra and quantum yield map of synthetic pheomelanin

被引:16
作者
Nighswander-Rempel, S. P. [1 ]
机构
[1] Univ Queensland, Ctr Biophoton & Laser Sci, Dept Phys, Brisbane, Qld 4067, Australia
关键词
photoluminescence; fluorescence emission; quantum yield; synthetic pheomelanin; benzothiazine; trichochromes;
D O I
10.1002/bip.20518
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spectroscopic studies of pheomelanin and its constituents have been sparse. These data present what is by far the most complete description of the fluorescence characteristics of synthetic pheomelanin. Emission spectra between 260 and 600 nm were acquired,for excitation wavelengths between 250 and 500 nm at 1-nm intervals. A quantum yield map is also presented, correcting the fluorescence intensities for differences in species concentration and molar absorptivity. These fluorescence features exhibit interesting similarities and differences to eumelanin, and these data are interpreted with respect to possible chemical structures. Overall, these data suggest that pheomelanin oligomers may be more tightly coupled than those of eumelanin. Finally, the quantum yield is shown to be on the order of 10(-4) and exhibit a complex dependence on excitation energy, varying by a factor of 4 across the energies employed here. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:631 / 637
页数:7
相关论文
共 33 条
[1]   EPIDEMIC TRICHOPHYTON-MENTAGROPHYTES INFECTIONS IN SERVICEMEN - SOURCE OF INFECTION, ROLE OF ENVIRONMENT, HOST FACTORS, AND SUSCEPTIBILITY [J].
ALLEN, AM ;
TAPLIN, D .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1973, 226 (08) :864-867
[2]   Geometric and spectroscopic study of some molecules related to eumelanins.: 1.: Monomers [J].
Bolívar-Marinez, LE ;
Galvao, DS ;
Caldas, MJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (15) :2993-3000
[3]  
BOMAN HG, 1981, TRENDS BIOCHEM SCI, V6, P306, DOI 10.1146/annurev.mi.41.100187.000535
[4]   The mole theory: primary function of melanocytes and melanin may be antimicrobial defense and immunomodulation (not solar protection) [J].
Burkhart, CG ;
Burkhart, CN .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2005, 44 (04) :340-342
[5]  
DEMAS JN, 1971, J PHYS CHEM-US, V75, P991, DOI 10.1021/j100678a001
[6]   Metal ions as potential regulatory factors in the biosynthesis of red hair pigments:: a new benzothiazole intermediate in the iron or copper assisted oxidation of 5-S-cysteinyldopa [J].
Di Donato, P ;
Napolitano, A ;
Prota, G .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1571 (02) :157-166
[7]  
Di Donato P, 2003, PIGM CELL RES, V16, P532
[8]   Autofluorescence of melanins induced by ultraviolet radiation and near ultraviolet light. A histochemical and biochemical study [J].
Elleder, M ;
Borovansky, J .
HISTOCHEMICAL JOURNAL, 2001, 33 (05) :273-281
[9]   Building blocks of eumelanin: Relative stability and excitation energies of tautomers of 5,6-dihydroxyindole and 5,6-indolequinone [J].
Il'ichev, YV ;
Simon, JD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (29) :7162-7171
[10]   QUANTITATIVE-ANALYSIS OF EUMELANIN AND PHEOMELANIN IN HAIR AND MELANOMAS [J].
ITO, S ;
JIMBOW, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 80 (04) :268-272