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用于靶向组蛋白H3的染色质结合蛋白动态分析的细胞内光催化邻近标记(iPPL)

Intracellular Photocatalytic Proximity Labeling (iPPL) for Dynamic Analysis of Chromatin-Binding Proteins Targeting Histone H3.

作者信息

Miura Kazuki, Niimi Hikaru, Niwa Tatsuya, Taguchi Hideki, Nakamura Hiroyuki

机构信息

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.

出版信息

ACS Chem Biol. 2024 Dec 20;19(12):2412-2417. doi: 10.1021/acschembio.4c00680. Epub 2024 Dec 9.

Abstract

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.

摘要

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。

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