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PMID: 19789711 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Physico-chemical evaluation of rationally designed melanins as novel nature-inspired radioprotectors.

PloS one ·Vol. 4 ·No. 9 ·2009-09-30 ·Pages e7229

Schweitzer AD, Howell RC, Jiang Z, Bryan RA, Gerfen G, Chen CC, Mah D, Cahill S, Casadevall A, Dadachova E

Abstract

Melanin, a high-molecular weight pigment that is ubiquitous in nature, protects melanized microorganisms against high doses of ionizing radiation. However, the physics of melanin interaction with ionizing radiation is unknown. We rationally designed melanins from either 5-S-cysteinyl-DOPA, L-cysteine/L-DOPA, or L-DOPA with diverse structures as shown by elemental analysis and HPLC. Sulfur-containing melanins had higher predicted attenuation coefficients than non-sulfur-containing melanins. All synthetic melanins displayed strong electron paramagnetic resonance (2.14.10(18), 7.09.10(18), and 9.05.10(17) spins/g, respectively), with sulfur-containing melanins demonstrating more complex spectra and higher numbers of stable free radicals. There was no change in the quality or quantity of the stable free radicals after high-dose (30,000 cGy), high-energy ((137)Cs, 661.6 keV) irradiation, indicating a high degree of radical stability as well as a robust resistance to the ionizing effects of gamma irradiation. The rationally designed melanins protected mammalian cells against ionizing radiation of different energies. We propose that due to melanin's numerous aromatic oligomers containing multiple pi-electron system, a generated Compton recoil electron gradually loses energy while passing through the pigment, until its energy is sufficiently low that it can be trapped by stable free radicals present in the pigment. Controlled dissipation of high-energy recoil electrons by melanin prevents secondary ionizations and the generation of damaging free radical species.

MeSH Terms
Animals CHO Cells Cricetinae Cricetulus Cryptococcus neoformans/metabolism Cysteine/chemistry Cysteinyldopa/chemistry Free Radicals Gamma Rays Levodopa/chemistry Manganese Compounds/pharmacology Melanins/metabolism,physiology Molecular Weight Oxides/pharmacology Oxygen/chemistry Radiation Tolerance Radiation, Ionizing
Chemicals
Free Radicals Manganese Compounds Melanins Oxides permanganic acid Cysteinyldopa Levodopa Cysteine Oxygen
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Schweitzer Andrew D
Department of Nuclear Medicine, Albert Einstein College of Medicine, New York, New York, United States of America.
Howell Robertha C
Jiang Zewei
Bryan Ruth A
Gerfen Gary
Chen Chin-Cheng
Mah Dennis
Cahill Sean
Casadevall Arturo
Dadachova Ekaterina
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2009-09-30
Epub
2009-00-30
Pages
e7229
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC2749938
Subset
IM
Grants
NIAID NIH HHS · AI52733 · United States
Howard Hughes Medical Institute · United States
NIAID NIH HHS · AI60507 · United States
NIAID NIH HHS · R01 AI052733 · United States
NIAID NIH HHS · R56 AI060507 · United States
NIAID NIH HHS · R01 AI060507 · United States
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