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Tandem application of cationic colloidal silica and Triton X-114 for plasma membrane protein isolation and purification: towards developing an MDCK protein database.
Mathias, Rommel A; Chen, Yuan-Shou; Goode, Robert J A; Kapp, Eugene A; Mathivanan, Suresh; Moritz, Robert L; Zhu, Hong-Jian; Simpson, Richard J.
Afiliación
  • Mathias RA; Ludwig Institute for Cancer Research, Parkville, Victoria, Australia.
Proteomics ; 11(7): 1238-53, 2011 Apr.
Article en En | MEDLINE | ID: mdl-21337516
Plasma membrane (PM) proteins are attractive therapeutic targets because of their accessibility to drugs. Although genes encoding PM proteins represent 20-30% of eukaryotic genomes, a detailed characterisation of their encoded proteins is underrepresented, due, to their low copy number and the inherent difficulties in their isolation and purification as a consequence of their high hydrophobicity. We describe here a strategy that combines two orthogonal methods to isolate and purify PM proteins from Madin Darby canine kidney (MDCK) cells. In this two-step method, we first used cationic colloidal silica (CCS) to isolate adherent (Ad) and non-adherent (nAd) PM fractions, and then subjected each fraction to Triton X-114 (TX-114) phase partitioning to further enrich for hydrophobic proteins. While CCS alone identified 255/757 (34%) membrane proteins, CCS/TX-114 in combination yielded 453/745 (61%). Strikingly, of those proteins unique to CCS/TX-114, 277/393 (70%) had membrane annotation. Further characterisation of the CCS/TX-114 data set using Uniprot and transmembrane hidden Markov model revealed that 306/745 (41%) contained one or more transmembrane domains (TMDs), including proteins with 25 and 17 TMDs. Of the remaining proteins in the data set, 69/439 (16%) are known to contain lipid modifications. Of all membrane proteins identified, 93 had PM origin, including proteins that mediate cell adhesion, modulate transmembrane ion transport, and cell-cell communication. These studies reveal that the application of CCS to first isolate Ad and nAd PM fractions, followed by their detergent-phase TX-114 partitioning, to be a powerful method to isolate low-abundance PM proteins, and a useful adjunct for in-depth cell surface proteome analyses.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Membrana Celular / Proteómica / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Proteomics Asunto de la revista: BIOQUIMICA Año: 2011 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Membrana Celular / Proteómica / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Proteomics Asunto de la revista: BIOQUIMICA Año: 2011 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Alemania