CHARACTERIZATION OF MELANOSOME-ASSOCIATED PROTEINS BY ESTABLISHMENT OF MONOCLONAL-ANTIBODIES AND IMMUNOSCREENING OF A MELANOMA CDNA LIBRARY THROUGH AN ANTI-MELANOSOME ANTIBODY

被引:5
作者
DAKOUR, J [1 ]
JIMBOW, K [1 ]
VINAYAGAMOORTHY, T [1 ]
LUO, D [1 ]
CHEN, H [1 ]
机构
[1] UNIV ALBERTA,FAC MED,HERITAGE MED RES CTR 260G,EDMONTON T6G 2S2,AB,CANADA
关键词
CDNA LIBRARY; MELANOSOME-ASSOCIATED PROTEINS; MONOCLONAL ANTIBODIES;
D O I
10.1097/00008390-199310000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Monoclonal antibodies against melanosomal components (human melanosome specific antigens; HMSAs) have been developed in our laboratory. HMSA-1-4 recognizes structural matrix proteins of melanosomes HMSA-5 is identical to TRP-1, equivalent to the b (brown) locus of murine melanocytes and expressed in early stages of melanosomal maturation. HMSA-6 is a protein associated with melanosomes but its role is still unclarified, and HMSA-7 is identical to the lysosomal protein CD63. We have also recently identified p90 calnexin-like, Ca2+-binding protein p97 melanotransferrin, rid p64 beta-D-galactosidase-like protein associated with melanosomes through immunological screening of our melanocytes (melanoma cells) cDNA library. Approximately 150 genes and 60 loci are known to influence eye, skin and hair colour in mammals. Tyrosinase is a rate-limiting enzyme responsible for melanin synthesis. In addition, tyrosine-related proteins (TRPs) and their genes have been identified and cloned. Tyrosinase and TRPS (e.g., TRP-1; b-locus protein identical to HMSA-5 and TRP-2; dopachrome tautomerase) are synthesized according to underlying genetic programmes, and are up- and/or down-regulated to create various forms of abnormal melanin pigmentation. We herein propose the importance of investigating the role of non-tyrosinase related proteins such as those which we have recently identified.
引用
收藏
页码:331 / 336
页数:6
相关论文
共 38 条
[1]  
Jimbow K., Quevedo W.C., Fitzpatrick T.B., Some aspects of melanin biology, J Invest Dermatol, 67, pp. 72-89, (1976)
[2]  
Jimbow K., Fitzpatrick T.B., Wick M.M., Biochemistry and physiology of melanin pigmentation, Physiology of Molecular Biology of the Skin, 2, pp. 873-909, (1991)
[3]  
Jimbow K., Fitzpatrick T.B., Characterization of a new melanosomal structural component—the vesiculoglobular body—by conventional transmission, high-voltage and scanning electron microscopy, J Ultrastruct Res, 48, pp. 269-283, (1974)
[4]  
Jimbow M., Kanoh H., Jimbow K., Characterization of biochemical properties of melanosomes for structural and functional differentiation: Analysis of the compositions of lipids and proteins in melanosomes and their subfractions, J Invest Dermatol, 79, pp. 97-103, (1982)
[5]  
Jimbow K., Fitzpatrick T.B., Quevedo W.C., Cascade of melanogenesis in epidermal melanin pigmentation. The melanosome as a programmed organelle, Structure and Function of Melanin, pp. 71-82, (1985)
[6]  
Imokawa G., Yada Y., Hori Y., Induction of melanization within hair bulb melanocytes in chinchilla mutant by melanogenic stimulants, J Invest Dermatol, 91, pp. 106-113, (1988)
[7]  
Hatta S., Mishima Y., Ichihashi M., Et al., Melanin monomers within coated vesicles and premelanosomes in melanin synthesizing cells, J Invest Dermatol, 91, pp. 181-184, (1988)
[8]  
Devi C.C., Tripathi R.K., Ramaiah A., PH-dependent interconvertible forms of mushroom tyrosinase with different kinetic properties, Pigment Cell Res, 2, pp. 8-13, (1989)
[9]  
Oikawa A., Saeki H., Akiyama T., Et al., Electron microscopic evidence for stimulation of melanosomal maturation by lysosomotropic agents and monensin in cultured B16 mouse melanoma cells, Pigment Cell Res, 1, pp. 44-50, (1987)
[10]  
Shibahara O., Tomita Y., Sakakura T., Et al., Cloning and expression of cDNA encoding mouse tyrosinase, Nucleic Acids Res, 14, pp. 2413-2427, (1986)