Construction and Screening of a Lentiviral Secretome Library

Cell Chem Biol. 2017 Jun 22;24(6):767-771.e3. doi: 10.1016/j.chembiol.2017.05.017. Epub 2017 Jun 9.

Abstract

Over 2,000 human proteins are predicted to be secreted, but the biological function of the many of these proteins is still unknown. Moreover, a number of these proteins may act as new therapeutic agents or be targets for the development of therapeutic antibodies. To further explore the extracellular proteome, we have developed a secretome-enriched open reading frame (ORF) library that can be readily screened for autocrine activity in cell-based phenotypic or reporter assays. Next-generation sequencing (NGS) and database analysis predict that the library contains approximately 900 ORFs encoding known secreted proteins (accounting for 77.8% of the library), as well as genes encoding potentially unknown secreted proteins. In a proof-of-principle study, human TF-1 cells were screened for proliferative factors, and the known cytokine GMCSF was identified as a dominant hit. This library offers a relatively low-cost and straightforward approach for functional autocrine screens of secreted proteins.

Keywords: autocrine; lentivirus; next-generation sequencing; open reading frame; secretome.

MeSH terms

  • Amino Acid Sequence
  • Gene Library*
  • Lentivirus / genetics*
  • Open Reading Frames / genetics
  • Phenotype
  • Proteome / chemistry
  • Proteome / genetics*
  • Proteome / metabolism*

Substances

  • Proteome