Miura Kazuki, Niimi Hikaru, Niwa Tatsuya, Taguchi Hideki, Nakamura Hiroyuki
Laboratory for Chemistry and Life Science, Institute of Integrated Research, Institute of Science Tokyo, Yokohama 226-8501, Japan.
School of Life Science and Technology, Institute of Science Tokyo, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.
ACS Chem Biol. 2024 Dec 20;19(12):2412-2417. doi: 10.1021/acschembio.4c00680. Epub 2024 Dec 9.
We demonstrated a novel approach for protein-protein interaction (PPI) profiling of histone H3 using intracellular photocatalytic-proximity labeling (iPPL). This approach identified that the combination of acriflavine as a photocatalyst and 1-methyl-4-arylurazol (MAUra) as a protein labeling agent was the most efficient strategy to proceed the protein proximity labeling reaction. Furthermore, the identification of the labeled amino acids in histone H3 interacting proteins, histone lysine -methyltransferase EZH2, showed that the amino acid in EZH2 within a few nanometers from histone H3 is labeled by iPPL. This restricted labeling radius allows for more-focused PPI profiling, compared to conventional proximity labeling methods.
我们展示了一种使用细胞内光催化邻近标记(iPPL)对组蛋白H3进行蛋白质-蛋白质相互作用(PPI)分析的新方法。该方法确定,吖啶黄作为光催化剂和1-甲基-4-芳基四唑(MAUra)作为蛋白质标记剂的组合是进行蛋白质邻近标记反应的最有效策略。此外,对与组蛋白H3相互作用的蛋白质——组蛋白赖氨酸甲基转移酶EZH2中标记氨基酸的鉴定表明,EZH2中距组蛋白H3几纳米内的氨基酸被iPPL标记。与传统的邻近标记方法相比,这种受限的标记半径允许进行更有针对性的PPI分析。