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1.
J Phys Chem B ; 110(28): 13985-90, 2006 Jul 20.
Artículo en Inglés | MEDLINE | ID: mdl-16836351

RESUMEN

We report a detailed photoluminescence study of cysteinyldopa-melanin (CDM), the synthetic analogue of pheomelanin. Emission spectra are shown to be a far more sensitive probe of CDM's spectroscopic behavior than are absorption spectra. Although CDM and dopa-melanin (DM, the synthetic analogue of eumelanin) have very similar absorption spectra, we find that they have very different excitation and emission characteristics; CDM has two distinct photoluminescence peaks that do not shift with excitation wavelength. Additionally, our data suggest that the radiative quantum yield of CDM is excitation energy dependent, an unusual property among biomolecules that is indicative of a chemically disordered system. Finally, we find that the radiative quantum yield for CDM is approximately 0.2%, twice that of DM, although still extremely low. This means that 99.8% of the energy absorbed by CDM is dissipated via nonradiative pathways, consistent with its role as a pigmentary photoprotectant.


Asunto(s)
Cisteinildopa/análogos & derivados , Melaninas/química , Cisteinildopa/química , Luminiscencia , Melaninas/síntesis química , Fotoquímica
2.
Soft Matter ; 2(1): 37-44, 2006 Dec 12.
Artículo en Inglés | MEDLINE | ID: mdl-32646091

RESUMEN

We discuss recent progress towards the establishment of important structure-property-function relationships in eumelanins-key functional bio-macromolecular systems responsible for photo-protection and immune response in humans, and implicated in the development of melanoma skin cancer. We focus on the link between eumelanin's secondary structure and optical properties such as broad band UV-visible absorption and strong non-radiative relaxation; both key features of the photo-protective function. We emphasise the insights gained through a holistic approach combining optical spectroscopy with first principles quantum chemical calculations, and advance the hypothesis that the robust functionality characteristic of eumelanin is related to extreme chemical and structural disorder at the secondary level. This inherent disorder is a low cost natural resource, and it is interesting to speculate as to whether it may play a role in other functional bio-macromolecular systems.

3.
J Phys Chem B ; 109(43): 20629-35, 2005 Nov 03.
Artículo en Inglés | MEDLINE | ID: mdl-16853670

RESUMEN

Previously reported excitation spectra for eumelanin are sparse and inconsistent. Moreover, these studies have failed to account for probe beam attenuation and emission reabsorption within the samples, making them qualitative at best. We report for the first time quantitative excitation spectra for synthetic eumelanin, acquired for a range of solution concentrations and emission wavelengths. Our data indicate that probe beam attenuation and emission reabsorption significantly affect the spectra even in low-concentration eumelanin solutions and that previously published data do not reflect the true excitation profile. We apply a correction procedure (previously applied to emission spectra) to account for these effects. Application of this procedure reconstructs the expected relationship of signal intensity with concentration, and the normalized spectra show a similarity in form to the absorption profiles. These spectra reveal valuable information regarding the photophysics and photochemistry of eumelanin. Most notably, an excitation peak at 365 nm (3.40 eV), whose position is independent of emission wavelength, is possibly attributable to a 5,6-dihydroxyindole-2-carboxylic acid (DHICA) component singly linked to a polymeric structure.


Asunto(s)
Melaninas/química , Espectrometría de Fluorescencia/métodos , Animales , Cabello/química , Humanos , Cinética , Melaninas/síntesis química , Retina/química , Espectrofotometría
4.
Spectrochim Acta A Mol Biomol Spectrosc ; 61(9): 2153-60, 2005 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15911405

RESUMEN

We report methods for correcting the photoluminescence emission and excitation spectra of highly absorbing samples for re-absorption and inner filter effects. We derive the general form of the correction, and investigate various methods for determining the parameters. Additionally, the correction methods are tested with highly absorbing fluorescein and melanin (broadband absorption) solutions; the expected linear relationships between absorption and emission are recovered upon application of the correction, indicating that the methods are valid. These procedures allow accurate quantitative analysis of the emission of low quantum yield samples (such as melanin) at concentrations where absorption is significant.


Asunto(s)
Melaninas/química , Absorción , Filtración , Fluoresceína/química , Mediciones Luminiscentes , Soluciones , Espectrometría de Fluorescencia , Espectrometría Raman
5.
Photochem Photobiol ; 79(2): 211-6, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-15068035

RESUMEN

We report absolute values for the radiative relaxation quantum yield of synthetic eumelanin as a function of excitation energy. These values were determined by correcting for pump beam attenuation and emission reabsorption in both eumelanin samples and fluorescein standards over a large range of concentrations. Our results confirm that eumelanins are capable of dissipating >99.9% of absorbed UV and visible radiation through nonradiative means. Furthermore, we have found that the radiative quantum yield of synthetic eumelanin is excitation energy dependent. This observation is supported by corrected emission spectra, which also show a clear dependence of both peak position and peak width on excitation energy. Our findings indicate that photoluminescence emission in eumelanins is derived from ensembles of small chemically distinct oligomeric units that can be selectively pumped. This hypothesis lends support to the theory that the basic structural unit of eumelanin is oligomeric rather than heteropolymeric.


Asunto(s)
Melaninas/química , Animales , Transferencia de Energía , Luz , Luminiscencia , Melaninas/síntesis química , Melaninas/efectos de la radiación , Fotoquímica , Teoría Cuántica , Espectrometría de Fluorescencia , Espectrofotometría
6.
Fertil Steril ; 93(2): 658-62, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19410247

RESUMEN

OBJECTIVE: To compare pronuclear morphology (Z-score), day 3 embryo grade, and day 3 cell number in the prediction of successful implantation rates (IRs), including cycles in which all or none of the embryos implanted. DESIGN: Retrospective analysis. SETTING: University-based IVF center. PATIENT(S): Four hundred twenty-six fresh IVF day 3 transfers of 852 embryos in women <36 years of age from January 2000 to December 2003 in whom all or none of the embryos implanted. MAIN OUTCOME MEASURE(S): Evaluation of Z-scores, embryo morphology, cell number, and IR. RESULT(S): Day 3 parameters were more predictive than Z-scores. When early parameters were poor (Z-score) but late parameters were both good, the IR was 38%, compared with 4% when the Z-score was good but the late parameters were poor. CONCLUSION(S): Embryo grading systems are useful in the prediction of embryo implantation. In particular, cell number and embryo grade are more predictive than Z-scores. Therefore, late parameters have a better prognostic value than Z-scores when selecting embryos for transfer.


Asunto(s)
Implantación del Embrión/fisiología , Embrión de Mamíferos/fisiología , Resultado del Embarazo/epidemiología , Adulto , División Celular , Embrión de Mamíferos/citología , Desarrollo Embrionario/fisiología , Femenino , Fertilización In Vitro/estadística & datos numéricos , Humanos , Valor Predictivo de las Pruebas , Embarazo , Estudios Retrospectivos
7.
Biophys J ; 90(11): 4137-44, 2006 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-16565050

RESUMEN

The optical scattering coefficient of a dilute, well-solubilized eumelanin solution has been accurately measured as a function of incident wavelength, and found to contribute <6% of the total optical attenuation between 210 and 325 nm. At longer wavelengths (325-800 nm), the scattering was less than the minimum sensitivity of our instrument. This indicates that ultraviolet and visible optical density spectra can be interpreted as true absorption with a high degree of confidence. The scattering coefficient versus wavelength was found to be consistent with Rayleigh theory for a particle radius of 38 +/- 1 nm. Our results shed important light on the role of melanins as photoprotectants.


Asunto(s)
Melaninas/química , Modelos Teóricos , Luz , Dispersión de Radiación , Soluciones/química , Análisis Espectral
8.
J Chem Phys ; 123(19): 194901, 2005 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-16321107

RESUMEN

The quantum yield of synthetic eumelanin is known to be extremely low and it has recently been reported to be dependent on excitation wavelength. In this paper, we present quantum yield as a function of excitation wavelength between 250 and 500 nm, showing it to be a factor of 4 higher at 250 nm than at 500 nm. In addition, we present a definitive map of the steady-state fluorescence as a function of excitation and emission wavelengths, and significantly, a three-dimensional map of the "specific quantum yield": the fraction of photons absorbed at each wavelength that are subsequently radiated at each emission wavelength. This map contains clear features, which we attribute to certain structural models, and shows that radiative emission and specific quantum yield are negligible at emission wavelengths outside the range of 585 and 385 nm (2.2 and 3.2 eV), regardless of excitation wavelength. This information is important in the context of understanding melanin biofunctionality, and the quantum molecular biophysics therein.


Asunto(s)
Melaninas/química , Biofisica/métodos , Transferencia de Energía , Humanos , Melanoma/metabolismo , Modelos Químicos , Modelos Estadísticos , Oxígeno/química , Fotoquímica , Fotones , Ingeniería de Proteínas/métodos , Teoría Cuántica , Neoplasias Cutáneas/patología , Espectrometría de Fluorescencia , Espectrofotometría Ultravioleta , Tirosina/química
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