The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The surface oxidation potential of human neuromelanin reveals a spherical architecture with a pheomelanin core and a eumelanin surface
Open accessAbstract
Neuromelanin (NM) isolated from the substantia nigra region of the human brain was studied by scanning probe and photoelectron emission microscopies. Atomic force microscopy reveals that NM granules are comprised of spherical structures with a diameter of ≈30 nm, similar to that observed for Sepia cuttlefish, bovine eye, and human eye and hair melanosomes. Photoelectron microscopy images were collected at specific wavelengths of UV light between 248 and 413 nm, using the spontaneous-emission output from the Duke OK-4 free electron laser. Analysis of the data establishes a threshold photoionization potential for NM of 4.5 ± 0.2 eV, which corresponds to an oxidation potential of −0.1 ± 0.2 V vs. the normal hydrogen electrode (NHE). The oxidation potential of NM is within experimental error of the oxidation potential measured for human eumelanosomes (−0.2 ± 0.2 V vs. NHE), despite the presence of a significant fraction of the red pigment, pheomelanin, which is characterized by a higher oxidation potential (+0.5 ± 0.2 V vs. NHE). Published kinetic studies on the early chemical steps of melanogenesis show that in the case of pigments containing a mixture of pheomelanin and eumelanin, of which NM is an example, pheomelanin formation occurs first with eumelanin formation predominantly occurring only after cysteine levels are depleted. Such a kinetic model would predict a structural motif with pheomelanin at the core and eumelanin at the surface, which is consistent with the measured surface oxidation potential of the ≈30-nm constituents of NM granules.
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Cites
Potential oxidative pathways of brain catecholamines
Tse, D. C. S., McCreery, R. L., & Adams, R. N. (1976) · Journal of Medicinal Chemistry · doi:10.1021/jm00223a008 · Cited by 415
Chemical degradation of melanins: Application to identification of dopamine-melanin
ITO, S., & WAKAMATSU, K. (1998) · Pigment Cell Research · doi:10.1111/j.1600-0749.1998.tb00721.x · Cited by 131
Ye, T., Hong, L., Garguilo, J., Pawlak, A., Edwards, G. S., Nemanich, R. J., Sarna, T., & Simon, J. D. (2006) · Photochemistry and Photobiology · doi:10.1562/2006-01-02-ra-762 · Cited by 81
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Cited by
Interactions of iron, dopamine and neuromelanin pathways in brain aging and Parkinson's disease
Zucca, F. A., Segura-Aguilar, J., Ferrari, E., Muñoz, P., Paris, I., Sulzer, D., Sarna, T., Casella, L., & Zecca, L. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.012 · Cited by 659
Self-citationSolano, F. (2014) · New Journal of Science · doi:10.1155/2014/498276 · Cited by 565
Chemistry of Mixed Melanogenesis—Pivotal Roles of Dopaquinone†
Ito, S., & Wakamatsu, K. (2008) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2007.00238.x · Cited by 503
Protective and toxic roles of dopamine in Parkinson's disease
Segura‐Aguilar, J., Paris, I., Muñoz, P., Ferrari, E., Zecca, L., & Zucca, F. A. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12686 · Cited by 498
Self-citationMelanins and melanogenesis: Methods, standards, protocols
d'Ischia, M., Wakamatsu, K., Napolitano, A., Briganti, S., Garcia‐Borron, J., Kovacs, D., Meredith, P., Pezzella, A., Picardo, M., Sarna, T., et al. (2013) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12121 · Cited by 484
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Metadata
- Authors
- Bush, W. D., Garguilo, J., Zucca, F. A., Albertini, A., Zecca, L., Edwards, G. S., Nemanich, R. J., & Simon, J. D.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2006-10-03
- Volume
- 103
- Issue
- 40
- Pages
- 14785-14789
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W1986351290
- Cited by
- 159
- References
- 3
- FWCI
- 3.25
- Type
- journal article
- Language
- en
- Open access
- green
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