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1.
J Cell Biochem ; 108(4): 877-85, 2009 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-19718658

RESUMO

A Disintegrin And Metalloprotease (ADAM15) is a member of the adamalysin protein family and has been associated with cancer, possibly via its role in ectodomain shedding of cadherins. Alternative mRNA splicing generates several ADAM15 isoforms containing different combinations of putative Src homology-3 (SH3) domain binding sites in their cytosolic tails. Here we present a comprehensive characterization of SH3 binding potential of different ADAM15 isoforms. Alternative use of ADAM15 exons was found to profoundly influence selection of SH3-containing cellular partner proteins, including the avid interactions with nephrocystin and sorting nexin-33 (SNX33 a.k.a. SNX30). Specifically, strong co-precipitation of nephrocystin from cell lysates was specific to ADAM15 isoforms i4, i5, and i6. These isoforms contain one or both of the two almost identical proline-rich regions encoded by exons 20 and 21, wherein the residues RxLPxxP were found to be indispensable for nephrocystin SH3 binding. Similarly, robust cellular association with SNX33 was observed only for ADAM15 isoforms containing the most carboxyterminal proline cluster lacking in isoforms i1 and i3. Thus, alternative mRNA splicing provides a versatile mechanism for regulation of intracellular protein interactions and thereby likely the cellular functions of ADAM15, which could explain the association with cancer of some but not all ADAM15 isoforms.


Assuntos
Proteínas ADAM/biossíntese , Proteínas ADAM/genética , Proteínas Adaptadoras de Transdução de Sinal/química , Processamento Alternativo , Proteínas de Transporte/química , Proteínas de Membrana/biossíntese , Proteínas de Membrana/química , Proteínas de Membrana/genética , Proteínas de Transporte Vesicular/química , Motivos de Aminoácidos , Linhagem Celular , Proteínas do Citoesqueleto , Humanos , Prolina/química , Regiões Promotoras Genéticas , Ligação Proteica , Isoformas de Proteínas , Estrutura Terciária de Proteína , RNA Mensageiro/metabolismo , Nexinas de Classificação , Domínios de Homologia de src
2.
J Chromatogr A ; 1028(2): 179-88, 2004 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-14989471

RESUMO

Brominated analogues (BMXs) of the strong drinking water mutagen MX (3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone) were found to be subject to strong matrix induced chromatographic response enhancement effects. We evaluated different ways to reduce errors in quantification including comparison of gas chromatographic inlet systems, improved clean up of sample extracts, and preparation of calibration standards in the sample matrix. The best quantitative accuracy and long term performance were achieved when the calibration standards were prepared in sample matrix, samples were cleaned up with C18-resin in conjunction with solid phase extraction (SPE) with Oasis HLB cartridges, and gas chromatography with PTV splitless injection was used. This method enables the determination of MX and BMXs from 500 ml water sample with quantitation limits of 1 ng/l or less.


Assuntos
Furanos/análise , Mutagênicos/análise , Poluentes Químicos da Água/análise , Bromo/química , Calibragem , Cromatografia Líquida de Alta Pressão , Cromatografia Gasosa-Espectrometria de Massas , Indicadores e Reagentes , Padrões de Referência , Soluções , Abastecimento de Água/análise
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