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Beads-free protein immunoprecipitation for a mass spectrometry-based interactome and posttranslational modifications analysis.
Mikula, Michal; Rubel, Tymon; Karczmarski, Jakub; Statkiewicz, Malgorzata; Bomsztyk, Karol; Ostrowski, Jerzy.
Afiliación
  • Mikula M; Department of Genetics, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, 02-781 Warsaw, Poland.
  • Rubel T; Institute of Radioelectronics, Warsaw University of Technology, 00-665 Warsaw, Poland.
  • Karczmarski J; Department of Genetics, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, 02-781 Warsaw, Poland.
  • Statkiewicz M; Department of Genetics, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, 02-781 Warsaw, Poland.
  • Bomsztyk K; Department of Medicine, University of Washington, Seattle, 98109 WA USA.
  • Ostrowski J; Department of Genetics, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, 02-781 Warsaw, Poland ; Department of Gastroenterology, Hepatology and Clinical Oncology, Medical Center for Postgraduate Education, 01-813 Warsaw, Poland.
Proteome Sci ; 13: 23, 2015.
Article en En | MEDLINE | ID: mdl-26336360
ABSTRACT

BACKGROUND:

Protein immunoprecipitation (IP) coupled with MS provides means to interrogate protein complexes and their posttranslational modifications (PTMs). In a typical protein IP assay antibodies are conjugated to protein A/G beads requiring large amounts of antibodies, tube transfers and centrifugations.

RESULTS:

As an alternative, we present Matrix-IP, beads-free microplate-based platform with surface-immobilized antibodies. Assay utilizes standard 96-well polypropylene PCR plates that are laboratory-fabricated with UV-C light and then protein A/G coated prior to IP reaction. We demonstrate application of Matrix-IP platform in MS analysis of heterogeneous nuclear ribonucleoprotein K (hnRNP K) interactome and PTMs.

CONCLUSION:

Matrix-IP is time-saving, easy to use high throughput method adaptable for low sample amounts and automation.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Proteome Sci Año: 2015 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Proteome Sci Año: 2015 Tipo del documento: Article País de afiliación: Polonia