Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein

被引:15
作者
Kus, Nicole J. [1 ]
Dolinska, Monika B. [1 ]
Young, Kenneth L., II [1 ]
Dimitriadis, Emilios K. [2 ]
Wingfield, Paul T. [3 ]
Sergeev, Yuri V. [1 ]
机构
[1] NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Biomed Imaging & Bioengn, Trans NIH Shared Resource Biomed Engn & Phys Sci, NIH, Bethesda, MD USA
[3] NIAMSD, Prot Express Lab, NIH, Bethesda, MD 20892 USA
关键词
OCULOCUTANEOUS ALBINISM TYPE-1; HYDROXYLASE; BINDING; BRENDA;
D O I
10.1371/journal.pone.0198247
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
07 ; 0710 ; 09 ;
摘要
Human tyrosinase (hTyr) is a Type 1 membrane bound glycoenzyme that catalyzes the initial and rate-limiting steps of melanin production in the melanosome. Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enzyme replacement therapy for a treatment of OCA1 is hampered by the absence of pure hTyr. Here, full-length hTyr (residues 1-529) was overexpressed in Trichoplusia ni larvae infected with a baculovirus, solubilized with detergent and purified using chromatography. Michaelis-Menten kinetics, enzymatic specific activity, and analytical ultracentrifugation were used to compare the hTyr in detergent with the soluble recombinant intra-melanosomal domain, hTyrC(tr) (residues 19-469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrC(tr), exhibited similar enzymatic activity and ligand affinity in L-DOPA and L-Tyrosine reactions. In addition, expression in larvae is a scalable process that will allow high yield protein production. Thus, larval production of enzymatically active human tyrosinase potentially could be a useful tool in developing a cure for OCA1.
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页数:11
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