The GM2 gangliosidoses are a group of recessive disorders, which lead to the accumulation of GM2 ganglioside in neuronal cells. The genes responsible for these disorders are HEXA (Tay-Sachs disease and variants), HEXB (Sandhoff disease and variants) and GM2A (AB variant of GM2 gangliosidosis). We have established three relational locus-specific databases recording allelic variation at the HEXA, HEXB and GM2A genes, and these can be accessed through the G M2 Gangliosidoses home page (http://data.mch.mcgill.ca/gm2-gangliosidoses/). The purpose of these databases is to collect and distribute information on mutations in the genes responsible for GM2 gangliosidosis. These databases are available online for users to search and retrieve information about specific mutations either by mutation, phenotype or author(s). In addition, submission forms are available for the addition of new mutations to the databases. / In order to provide information concerning the effects of mutations on the manifestations of disease, we proceeded to model on the theoretical model of the alpha subunit a few missense mutations. (Abstract shortened by UMI.)

No description available.

Made available in DSpace on 2014-12-17T14:03:43Z (GMT). No. of bitstreams: 1 AdilaLML.pdf: 743306 bytes, checksum: 8c2b4b2827dafcc2f2edd7664a266e10 (MD5) Previous issue date: 2006-11-30 / Two b-N-acetylhexosaminidases (F11 e F15) were purified from Echinometra lucunter gonads extracts. The purified enzymes were obtained using ammonium sulfate fractionation, followed by gel filtration chromatographies (Sephacryl S-200, Sephadex G-75 and Sephacryl S-200). The F11 fraction was purified 192.47 -fold with a 28.5% yield, and F15 fraction 85.41 -fold with a 32.3% yield. The molecular weights of the fractions were 116 kDa for F11 and 42 kDa for F15 using SDS-PAGE. In Sephacryl S-200, F15 was 84 kDa, indicating that it is a dimeric protein. When p-nitrophenyl-?-D-glycosaminide was used as substrate, we determined an apparent Km of 0.257 mM and Vmax of 0.704 for F11 and for F15 the Km was 0.235 mM and Vmax of 0.9 mM of product liberated by hour. Both enzymes have optimum pH and temperature respectively at 5.0 and 45 ?C. The enzymes showed inhibition by silver nitrate, while the glucuronic acid was a potent activator. The high inhibition of F15 by N-etylmaleimide indicates that sulphydril groups are involved in the catalysis of synthetic substrate / Neste trabalho foram purificadas e caracterizadas parcialmente duas N-acetil-b- hexosaminidases (F11 e F15) extra?das de g?nadas do equinoderma marinho Echinometra lucunter. As enzimas foram purificadas com protocolo seq?encial por precipita??o com sulfato de am?nio e cromatografias de exclus?o molecular (Sephacryl S-200, Sephadex G-75 e Sephacryl S-200). A fra??o F11 foi purificada 192,47 vezes com recupera??o de 28,5% e F15 85,41 vezes com recupera??o de 32,3%. Suas massas moleculares, determinadas por eletroforese em gel de poliacrilamida com SDS, foram respectivamente 116 e 42 kDa. Em Sephacryl S-200 F15 apresentou massa molecular de 84 KDa, sugerindo que esta enzima possui forma dim?rica. Utilizando-se p-nitrofenil N-acetil-b-glicosamin?deo como substrato obtivemos Km aparente de 0,257 mM e Vmax de 0,704 unidades de absorb?ncia a 405 nm / h para a fra??o 11, e 0,235 mM e Vmax de 0,9 unidades de absorb?ncia a 405 nm / h para F15. Ambas fra??es apresentaram pH e a temperatura ?tima de cat?lise 5,0 e 45 ?C, respectivamente. A atividade N-acetil-b-glicosaminid?sica foi potencialmente inibida por prata, iodoacetamida, N-etilmaleimida e PMSF. A forte inibi??o de F15 por N-etilmaleimida indica o envolvimento de radicais sulfidrila na hidr?lise do substrato sint?tico, caracterizando tamb?m ser uma enzima altamente sensitiva a este sal