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J Am Chem Soc ; 134(40): 16891-8, 2012 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-22992158

RESUMO

Peptides have been site-selectively placed on microelectrode arrays with the use of both thiol-based conjugate additions and Cu(I)-coupling reactions between thiols and aryl halides. The conjugate addition reactions used both acrylate and maleimide Michael acceptors. Of the two methods, the Cu(I)-coupling reactions proved far superior because of their irreversibility. Surfaces constructed with the conjugate addition chemistry were not stable at neutral pHs, especially the surface using the maleimide acceptor. Once a peptide was placed onto the array, it could be monitored in "real-time" for its interactions with a biological receptor.


Assuntos
Peptídeos/química , Análise Serial de Proteínas/instrumentação , Compostos de Sulfidrila/química , Acrilatos/química , Cobre/química , Desenho de Equipamento , Maleimidas/química , Microeletrodos , Oligopeptídeos/química , Oligopeptídeos/metabolismo , Peptídeos/metabolismo
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