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Monitoring Two-Component Sensor Kinases with a Chemotaxis Signal Readout.
Lai, Run-Zhi; Parkinson, John S.
Afiliação
  • Lai RZ; Department of Biology, University of Utah, Salt Lake City, UT, USA.
  • Parkinson JS; Department of Biology, University of Utah, Salt Lake City, UT, USA. parkinson@biology.utah.edu.
Methods Mol Biol ; 1729: 127-135, 2018.
Article em En | MEDLINE | ID: mdl-29429088
Bacteria use two-component signal transduction systems to elicit adaptive responses to environmental changes. The simplest of these systems comprises a transmembrane sensor with histidine kinase activity and its cytoplasmic response regulator partner. Stimulus-response studies of two-component signaling systems typically employ expression reporters, such as ß-galactosidase, that operate with relatively slow kinetics and low precision. In this chapter, we illustrate a new strategy for directly measuring the signaling activities of two-component sensor kinases in vivo. Our method exploits recent work that defines the recognition determinants for sensor-response regulator signaling transactions, which enabled us to couple histidine kinases to a FRET-based assay that uses signaling components of the E. coli chemotaxis system. We demonstrate the approach with NarX, a nitrate/nitrite sensor kinase, but the method should be applicable to other two-component sensor kinases.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Proteínas Quinases / Proteínas de Escherichia coli / Escherichia coli / Histidina Quinase Idioma: En Revista: Methods Mol Biol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Proteínas Quinases / Proteínas de Escherichia coli / Escherichia coli / Histidina Quinase Idioma: En Revista: Methods Mol Biol Ano de publicação: 2018 Tipo de documento: Article