Your browser doesn't support javascript.
loading
Tissue Washing Improves Native Ambient Mass Spectrometry Detection of Membrane Proteins Directly from Tissue.
Sisley, Emma K; Hale, Oliver J; Hughes, James W; Cooper, Helen J.
Afiliación
  • Sisley EK; School of Biosciences, University of Birmingham, Birmingham B15 2TT, U.K.
  • Hale OJ; School of Biosciences, University of Birmingham, Birmingham B15 2TT, U.K.
  • Hughes JW; School of Biosciences, University of Birmingham, Birmingham B15 2TT, U.K.
  • Cooper HJ; School of Biosciences, University of Birmingham, Birmingham B15 2TT, U.K.
J Am Chem Soc ; 145(29): 15658-15662, 2023 07 26.
Article en En | MEDLINE | ID: mdl-37459360
ABSTRACT
Native ambient mass spectrometry enables the in situ analysis of proteins and their complexes directly from tissue, providing both structural and spatial information. Until recently, the approach was applied exclusively to the analysis of soluble proteins; however, there is a drive for new techniques that enable analysis of membrane proteins. Here we demonstrate native ambient mass spectrometry of membrane proteins, including ß-barrel and α-helical (single and multipass) integral membrane proteins and membrane-associated proteins incorporating lipid anchors, by integration of a simple washing protocol to remove soluble proteins. Mass spectrometry imaging revealed that washing did not disrupt the spatial distributions of the membrane and membrane-associated proteins. Some delocalization of the remaining soluble proteins was observed.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de la Membrana Tipo de estudio: Diagnostic_studies Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de la Membrana Tipo de estudio: Diagnostic_studies Idioma: En Año: 2023 Tipo del documento: Article