The repeat domain of the melanosome fibril protein Pmel17 forms the amyloid core promoting melanin synthesis

被引:112
作者
McGlinchey, Ryan P. [1 ]
Shewmaker, Frank [1 ]
McPhie, Peter [1 ]
Monterroso, Begona [1 ]
Thurber, Kent [2 ]
Wickner, Reed B. [1 ]
机构
[1] NIDDKD, Lab Biochem & Genent, NIH, Bethesda, MD 20892 USA
[2] NIDDKD, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
关键词
SOLID-STATE NMR; BETA-SHEET STRUCTURE; NUCLEAR-MAGNETIC-RESONANCE; PRION-INDUCING DOMAIN; PINK-EYED DILUTION; HET-S PRION; IN-VITRO; PARALLEL; ORGANIZATION; PH;
D O I
10.1073/pnas.0906509106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Pmel17 is a melanocyte protein necessary for eumelanin deposition 1 in mammals and found in melanosomes in a filamentous form. The luminal part of human Pmel17 includes a region (RPT) with 10 copies of a partial repeat sequence, pt.e.gttp.qv., known to be essential in vivo for filament formation. We show that this RPT region readily forms amyloid in vitro, but only under the mildly acidic conditions typical of the lysosome-like melanosome lumen, and the filaments quickly become soluble at neutral pH. Under the same mildly acidic conditions, the Pmel filaments promote eumelanin formation. Electron diffraction, circular dichroism, and solid-state NMR studies of Pmel17 filaments show that the structure is rich in beta sheet. We suggest that RPT is the amyloid core domain of the Pmel17 filaments so critical for melanin formation.
引用
收藏
页码:13731 / 13736
页数:6
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