Expression of LY6D is induced at the surface of MCF10A cells by X-ray irradiation

FEBS J. 2012 Dec;279(24):4479-91. doi: 10.1111/febs.12034. Epub 2012 Nov 22.

Abstract

In order to identify membrane proteins whose expression is induced by X-ray irradiation, we developed an antibody (Ab)-directed strategy using a phage Ab library. X-Ray-irradiated cells were screened with a phage Ab library in the presence of a large excess of polyclonal Abs prepared against membrane proteins that are commonly present at the surface of both X-ray-irradiated and nonirradiated cells. After isolation of Ab that bound only to X-ray-irradiated cells, the antigen was identified using MS. Using this approach, we found that expression of LY6D is induced in MCF10A cells by X-ray irradiation. The induction of LY6D expression is triggered through a pathway regulated by ATM, CHK2 and p53. This method is a new Ab-directed proteomic strategy for analysis of membrane proteins, and is applicable to various biological phenomena in situations in which both target molecule-expressing cells and nonexpressing cells are available.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins
  • Base Sequence
  • Cell Adhesion Molecules / biosynthesis*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / immunology
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Checkpoint Kinase 2
  • DNA Primers
  • DNA-Binding Proteins / metabolism
  • GPI-Linked Proteins / biosynthesis
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / immunology
  • Humans
  • Mutagens / toxicity
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • RNA, Small Interfering
  • Real-Time Polymerase Chain Reaction
  • Transcription, Genetic
  • Tumor Suppressor Protein p53 / metabolism
  • Tumor Suppressor Proteins / metabolism
  • X-Rays*

Substances

  • Cell Adhesion Molecules
  • Cell Cycle Proteins
  • DNA Primers
  • DNA-Binding Proteins
  • GPI-Linked Proteins
  • LY6D protein, human
  • Mutagens
  • RNA, Small Interfering
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • Checkpoint Kinase 2
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • CHEK2 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins p21(ras)