Solution structure of copper ion-induced molecular aggregates of tyrosine melanin

被引:91
作者
Gallas, JM
Littrell, KC
Seifert, S
Zajac, GW
Thiyagarajan, P
机构
[1] Univ Texas, Div Phys & Earth Sci, San Antonio, TX 78249 USA
[2] Argonne Natl Lab, Intense Pulsed Neutron Source, Argonne, IL 60439 USA
[3] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[4] Amoco Res Ctr, Naperville, IL 60566 USA
关键词
D O I
10.1016/S0006-3495(99)76964-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Melanin, the ubiquitous biological pigment, provides photoprotection by efficient filtration of light and also by its antioxidant behavior. In solutions of synthetic melanin, both optical and antioxidant behavior are affected by the aggregation states of melanin. We have utilized small-angle x-ray and neutron scattering to determine the molecular dimensions of synthetic tyrosine melanin in its unaggregated state in D2O and H2O to study the structure of melanin aggregates formed in the presence of copper ions at various copper-to-melanin molar ratios. In the absence of copper ions, or at low copper ion concentrations, tyrosine melanin is present in solution as a sheet-like particle with a mean thickness of 12.5 Angstrom and a lateral extent of similar to 54 Angstrom. At a copper-to-melanin molar ratio of 0.6, melanin aggregates to form long, rod-like structures with a radius of 32 Angstrom. At a higher copper ion concentration, with a copper-to-melanin ratio of 1.0, these rod-like structures further aggregate, forming sheet-like structures with a mean thickness of 51 Angstrom. A change in the charge of the ionizable groups induced by the addition of copper ions is proposed to account for part of the aggregation. The data also support a model for the copper-induced aggregation of melanin driven by rr stacking assisted by peripheral Cu2+ complexation. The relationship between our results and a previous hypothesis for reduced cellular damage from bound-to-melanin redox metal ions is also discussed.
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页码:1135 / 1142
页数:8
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