Quantification of Ca2+ binding to melanin supports the hypothesis that melanosomes serve a functional role in regulating calcium homeostasis
被引:71
作者:
Bush, William D.
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机构:Duke Univ, Dept Chem, Durham, NC 27706 USA
Bush, William D.
Simon, John D.
论文数: 0引用数: 0
h-index: 0
机构:
Duke Univ, Dept Chem, Durham, NC 27706 USADuke Univ, Dept Chem, Durham, NC 27706 USA
Simon, John D.
[1
]
机构:
[1] Duke Univ, Dept Chem, Durham, NC 27706 USA
[2] Duke Univ, Dept Biochem & Ophthalmol, Med Ctr, Durham, NC 27706 USA
来源:
PIGMENT CELL RESEARCH
|
2007年
/
20卷
/
02期
关键词:
calcium;
melanin;
Sepia;
isothermaI titration;
calorimetry;
association constant;
pKa;
D O I:
10.1111/j.1600-0749.2007.00362.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Calcium regulation in melanocytes affects numerous biological pathways including protecting the redox balance in the cell and regulating the supply of substrate, L-tyrosine, for melanogenesis. The pigment contained in the melanocytes, melanin, has been implicated in maintaining calcium homeostasis in the cell and is known to be involved with calcium ion regulation in the inner ear. Herein, the association constant for Ca2+ binding to Sepia melanin is determined by isothermal titration calorimetry to be 3.3 (+/- 0.2) x 10(3)/M. This value is comparable with other well-established intracellular calcium-binding proteins that serve to buffer calcium concentrations, lending further support to the hypothesis that melanosomes serve as intracellular mediators of calcium homeostasis in melanocytes. Using this binding constant and the data from a fluorescent Ca2+ displacement assay, the pK. of the carboxyl group coordinated to Ca2+ is determined to be 3.1 +/- 0.1.