Complementary Proteomic Tools for the Dissection of Apoptotic Proteolysis Events
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- 作者：Victoria C. Pham ; Robert Pitti ; Veronica G. Anania ; Corey E. Bakalarski ; Daisy Bustos ; Suchit Jhunjhunwala ; Qui T. Phung ; Kebing Yu ; William F. Forrest ; Donald S. Kirkpatrick ; Avi Ashkenazi ; Jennie R. Lill
- 刊名：Journal of Proteome Research
- 出版年：2012
- 出版时间：May 4, 2012
- 年：2012
- 卷：11
- 期：5
- 页码：2947-2954
- 全文大小：433K
- 年卷期：v.11,no.5(May 4, 2012)
- ISSN：1535-3907
文摘
Proteolysis is a key regulatory event that controls intracellular and extracellular signaling through irreversible changes in a protein鈥檚 structure that greatly alters its function. Here we describe a platform for profiling caspase substrates which encompasses two highly complementary proteomic techniques鈥攖he first is a differential gel based approach termed Global Analyzer of SILAC-derived Substrates of Proteolysis (GASSP) and the second involves affinity enrichment of peptides containing a C-terminal aspartic acid residue. In combination, these techniques have enabled the profiling of a large cellular pool of apoptotic-mediated proteolytic events across a wide dynamic range. By applying this integrated proteomic work flow to analyze proteolytic events resulting from the induction of intrinsic apoptosis in Jurkat cells via etoposide treatment, 3346 proteins were quantified, of which 360 proteins were identified as etoposide-induced proteolytic substrates, including 160 previously assigned caspase substrates. In addition to global profiling, a targeted approach using BAX HCT116 isogenic cell lines was utilized to dissect pre- and post-mitochondrial extrinsic apoptotic cleavage events. By employing apoptotic activation with a pro-apoptotic receptor agonist (PARA), a limited set of apoptotic substrates including known caspase substrates such as BH3 interacting-domain death agonist (BID) and Poly (ADP-ribose) polymerase (PARP)-1, and novel substrates such as Basic Transcription Factor 3, TRK-fused gene protein (TFG), and p62/Sequestosome were also identified.