| Literature DB >> 26548958 |
Chieri Ida1, Sachiko Yamashita2, Masaki Tsukada2, Teruaki Sato2, Takayuki Eguchi2, Masakazu Tanaka3, Shin Ogata4, Takahiro Fujii2, Yoshisuke Nishi2, Susumu Ikegami2, Joel Moss5, Masanao Miwa6.
Abstract
PolyADP-ribosylation is mediated by poly(ADP-ribose) (PAR) polymerases (PARPs) and may be involved in various cellular events, including chromosomal stability, DNA repair, transcription, cell death, and differentiation. The physiological level of PAR is difficult to determine in intact cells because of the rapid synthesis of PAR by PARPs and the breakdown of PAR by PAR-degrading enzymes, including poly(ADP-ribose) glycohydrolase (PARG) and ADP-ribosylhydrolase 3. Artifactual synthesis and/or degradation of PAR likely occurs during lysis of cells in culture. We developed a sensitive enzyme-linked immunosorbent assay (ELISA) to measure the physiological levels of PAR in cultured cells. We immediately inactivated enzymes that catalyze the synthesis and degradation of PAR. We validated that trichloroacetic acid is suitable for inactivating PARPs, PARG, and other enzymes involved in metabolizing PAR in cultured cells during cell lysis. The PAR level in cells harvested with the standard radioimmunoprecipitation assay buffer was increased by 450-fold compared with trichloroacetic acid for lysis, presumably because of activation of PARPs by DNA damage that occurred during cell lysis. This ELISA can be used to analyze the biological functions of polyADP-ribosylation under various physiological conditions in cultured cells.Entities:
Keywords: Antibody; ELISA; HeLa cells; Poly(ADP-ribose) glycohydrolase; Poly(ADP-ribose) polymerase
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Year: 2015 PMID: 26548958 PMCID: PMC6118347 DOI: 10.1016/j.ab.2015.10.014
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365