Recent advances in the chemistry of melanogenesis in mammals
- PMID: 6771336
- DOI: 10.1111/1523-1747.ep12521344
Recent advances in the chemistry of melanogenesis in mammals
Abstract
The color of mammalian hair, skin, and eyes results mainly from the secretory products of melanocytes. These secretory products consist of a wide range of melanin pigments with different structures and compositions. These include black or brown nitrogenous eumelanins; yellow or reddish brown, sulfur-containing pheomelanins, e.g., the trichochromes of low molecular weight; and other pigments whose chemical and physical properties are intermediate between those of typical eumelanins and pheomelanins. Despite the evident differences in molecular size and general properties, all these pigments are biogenetically related, and they arise from a common mmetabolic pathway in which dopaquinone is the key intermediate. The current state of knowledge on the molecular mechanisms governing the etabolic fate of dopaquinone in melanocytes is discussed with special reference to the role of such sulfhydryl compounds as cysteine and glutathione in melanogenesis.
Similar articles
-
Chemical characterization of pheomelanogenesis starting from dihydroxyphenylalanine or tyrosine and cysteine. Effects of tyrosinase and cysteine concentrations and reaction time.Biochim Biophys Acta. 1997 Oct 20;1336(3):539-48. doi: 10.1016/s0304-4165(97)00068-8. Biochim Biophys Acta. 1997. PMID: 9367182
-
From tyrosine to melanin: Signaling pathways and factors regulating melanogenesis.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.
-
Incorporation of sulfhydryl compounds into melanins in vitro.Biochim Biophys Acta. 1988 Jan 12;964(1):1-7. doi: 10.1016/0304-4165(88)90060-8. Biochim Biophys Acta. 1988. PMID: 3120789
-
The role of sulfhydryl compounds in mammalian melanogenesis: the effect of cysteine and glutathione upon tyrosinase and the intermediates of the pathway.Biochim Biophys Acta. 1988 Nov 17;967(2):296-303. doi: 10.1016/0304-4165(88)90023-2. Biochim Biophys Acta. 1988. PMID: 2903772
-
Chemistry of mixed melanogenesis--pivotal roles of dopaquinone.Photochem Photobiol. 2008 May-Jun;84(3):582-92. doi: 10.1111/j.1751-1097.2007.00238.x. Photochem Photobiol. 2008. PMID: 18435614 Review.
Cited by
-
Semiquinone anion radicals of catechol(amine)s, catechol estrogens, and their metal ion complexes.Environ Health Perspect. 1985 Dec;64:185-98. doi: 10.1289/ehp.8564185. Environ Health Perspect. 1985. PMID: 3007089 Free PMC article.
-
Glyphosate inhibits melanization and increases susceptibility to infection in insects.PLoS Biol. 2021 May 12;19(5):e3001182. doi: 10.1371/journal.pbio.3001182. eCollection 2021 May. PLoS Biol. 2021. PMID: 33979323 Free PMC article.
-
Structural, electrical, electronic and optical properties of melanin films.Eur Phys J E Soft Matter. 2009 Mar;28(3):285-91. doi: 10.1140/epje/i2008-10437-9. Epub 2009 Feb 3. Eur Phys J E Soft Matter. 2009. PMID: 19190947
-
The protein oxidation product 3,4-dihydroxyphenylalanine (DOPA) mediates oxidative DNA damage.Biochem J. 1998 Mar 15;330 ( Pt 3)(Pt 3):1059-67. doi: 10.1042/bj3301059. Biochem J. 1998. PMID: 9494069 Free PMC article.
-
Oxidation of tyrosine residues in proteins by tyrosinase. Formation of protein-bonded 3,4-dihydroxyphenylalanine and 5-S-cysteinyl-3,4-dihydroxyphenylalanine.Biochem J. 1984 Sep 1;222(2):407-11. doi: 10.1042/bj2220407. Biochem J. 1984. PMID: 6433900 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources