Proximity Histidine Labeling by Umpolung Strategy Using Singlet Oxygen

被引:66
|
作者
Nakane, Keita [1 ]
Sato, Shinichi [1 ,4 ]
Niwa, Tatsuya [2 ]
Tsushima, Michihiko [3 ]
Tomoshige, Shusuke [1 ]
Taguchi, Hideki [2 ]
Ishikawa, Minoru [1 ]
Nakamura, Hiroyuki [3 ]
机构
[1] Tohoku Univ, Grad Sch Life Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
[2] Tokyo Inst Technol, Inst Innovat Res, Cell Biol Ctr, Yokohama, Kanagawa 2268503, Japan
[3] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Yokohama, Kanagawa 2268503, Japan
[4] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
关键词
TARGET PROTEIN; OXIDATION; DISCOVERY;
D O I
10.1021/jacs.1c01626
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While electrophilic reagents for histidine labeling have been developed, we report an umpolung strategy for histidine functionalization. A nucleophilic small molecule, 1-methyl-4-arylurazole, selectively labeled histidine under singlet oxygen (O-1(2)) generation conditions. Rapid histidine labeling can be applied for instant protein labeling. Utilizing the short diffusion distance of O-1(2) and a technique to localize the O-1(2) generator, a photocatalyst in close proximity to the ligand-binding site, we demonstrated antibody Fc-selective labeling on magnetic beads functionalized with a ruthenium photocatalyst and Fc ligand, ApA. Three histidine residues located around the ApA binding site were identified as labeling sites by liquid chromatography-mass spectrometry analysis. This result suggests that O-1(2)-mediated histidine labeling can be applied to a proximity labeling reaction on the nanometer scale.
引用
收藏
页码:7726 / 7731
页数:6
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