A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1) - PubMed (original) (raw)
. 1994 Jul 8;269(27):17993-8000.
Affiliations
- PMID: 8027058
Free article
A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1)
C Jiménez-Cervantes et al. J Biol Chem. 1994.
Free article
Abstract
Since the characterization of 5,6-dihydroxyindole-2-carboxylic acid (DHICA) as a major melanogenic intermediate, the fate of this compound and the mechanisms of its incorporation into the melanin polymer have become major issues in the study of melanogenesis. DHICA is a stable dihydroxyindole with a low rate of spontaneous oxidation, suggesting that enzymatic mechanism(s) might contribute to its evolution. The most obvious candidates are the melanosomal tyrosinases. We have recently shown that mouse melanosomes contain two electrophoretically distinct tyrosinase isoenzymes, termed low electrophoretic mobility tyrosinase (LEMT) and high electrophoretic mobility tyrosinase (HEMT), that can be resolved and purified. In this study, we report immunological evidence indicating that LEMT corresponds to the protein encoded by the brown locus (termed tyrosinase-related protein-1, TRP1), while HEMT corresponds to the tyrosinase encoded by the albino locus. We have compared the ability of both isoenzymes to catalyze DHICA evolution as determined by high performance liquid chromatography; although LEMT is a relatively poor tyrosine hydroxylase and DOPA oxidase as compared to HEMT, it was readily able to accelerate DHICA consumption concomitant with the production of a brownish product. However, the DHICA conversion activity of HEMT was barely detectable. The ability of purified LEMT to catalyze DHICA conversion could be almost completely abolished by treatment with heat or trypsin, and was inhibited in a concentration dependent way by the tyrosinase inhibitor 2-phenylthiourea and by L-tyrosine. Moreover, in the presence of low concentration of ascorbate, the DHICA conversion activity of LEMT displayed a lag period which was progressively longer at higher ascorbate concentrations. Based on the relationship between ascorbate added, enzyme activity, and lag period, it is very likely that the DHICA converting activity is indeed a DHICA oxidase activity. This was further proven by the demonstration that the product reacts rapidly and efficiently with the quinone trapping reagent 3-methyl-2-benzothiazolinone hydrazone, yielding a colored adduct similar to the one obtained with DOPAquinone. The DHICA oxidase activity of LEMT displayed a Km for DHICA of about 0.8 mM, as compared to 1.9 mM for L-DOPA and 0.23 nM for L-tyrosine. These results suggest that TRP1, the product of the brown locus, is indeed a tyrosinase with DHICA oxidase activity. However, as opposed to the tyrosinase encoded by the albino locus, TRP1's role in melanogenesis could be more directly related to DHICA metabolism than to the first steps of the pathway.
Similar articles
- The DHICA oxidase activity of the melanosomal tyrosinases LEMT and HEMT.
Jiménez-Cervantes C, Solano F, Lozano JA, García-Borrón JC. Jiménez-Cervantes C, et al. Pigment Cell Res. 1994 Oct;7(5):298-304. doi: 10.1111/j.1600-0749.1994.tb00631.x. Pigment Cell Res. 1994. PMID: 7886002 - Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis.
Kobayashi T, Urabe K, Winder A, Jiménez-Cervantes C, Imokawa G, Brewington T, Solano F, García-Borrón JC, Hearing VJ. Kobayashi T, et al. EMBO J. 1994 Dec 15;13(24):5818-25. doi: 10.1002/j.1460-2075.1994.tb06925.x. EMBO J. 1994. PMID: 7813420 Free PMC article. - The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase.
Olivares C, Jiménez-Cervantes C, Lozano JA, Solano F, García-Borrón JC. Olivares C, et al. Biochem J. 2001 Feb 15;354(Pt 1):131-9. doi: 10.1042/0264-6021:3540131. Biochem J. 2001. PMID: 11171088 Free PMC article. - Molecular and biological control of melanogenesis through tyrosinase genes and intrinsic and extrinsic regulatory factors.
Mishima Y. Mishima Y. Pigment Cell Res. 1994 Dec;7(6):376-87. doi: 10.1111/j.1600-0749.1994.tb00065.x. Pigment Cell Res. 1994. PMID: 7761345 Review. - From tyrosine to melanin: Signaling pathways and factors regulating melanogenesis.
Rzepka Z, Buszman E, Beberok A, Wrześniok D. Rzepka Z, et al. Postepy Hig Med Dosw (Online). 2016 Jun 30;70(0):695-708. doi: 10.5604/17322693.1208033. Postepy Hig Med Dosw (Online). 2016. PMID: 27356601 Review.
Cited by
- Malignant Melanoma: An Overview, New Perspectives, and Vitamin D Signaling.
Slominski RM, Kim TK, Janjetovic Z, Brożyna AA, Podgorska E, Dixon KM, Mason RS, Tuckey RC, Sharma R, Crossman DK, Elmets C, Raman C, Jetten AM, Indra AK, Slominski AT. Slominski RM, et al. Cancers (Basel). 2024 Jun 18;16(12):2262. doi: 10.3390/cancers16122262. Cancers (Basel). 2024. PMID: 38927967 Free PMC article. Review. - Inhibitory Effects of Fermented Sprouted Oat Extracts on Oxidative Stress and Melanin Overproduction.
Cho H, Yang J, Kang JY, Kim KE. Cho H, et al. Antioxidants (Basel). 2024 Apr 29;13(5):544. doi: 10.3390/antiox13050544. Antioxidants (Basel). 2024. PMID: 38790649 Free PMC article. - Comparative Studies on the Photoreactivity, Efficacy, and Safety of Depigmenting Agents.
Mota S, Rosa GP, Barreto MC, Garrido J, Sousa E, Cruz MT, Almeida IF, Quintas C. Mota S, et al. Pharmaceuticals (Basel). 2023 Dec 28;17(1):55. doi: 10.3390/ph17010055. Pharmaceuticals (Basel). 2023. PMID: 38256889 Free PMC article. - Phenotype transition from wild mouflon to domestic sheep.
Mereu P, Pirastru M, Sanna D, Bassu G, Naitana S, Leoni GG. Mereu P, et al. Genet Sel Evol. 2024 Jan 2;56(1):1. doi: 10.1186/s12711-023-00871-6. Genet Sel Evol. 2024. PMID: 38166592 Free PMC article. Review. - Aspacochioside C from Asparagus cochinchinensis attenuates eumelanin synthesis via inhibition of TRP2 expression.
Yunmam S, Lee HR, Hong SM, Kim JY, Kang TH, Lee AY, Jang DS, Kim SY. Yunmam S, et al. Sci Rep. 2023 Sep 8;13(1):14831. doi: 10.1038/s41598-023-41248-5. Sci Rep. 2023. PMID: 37684311 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials