双吖丙啶
化学
细胞内
标签
费斯特共振能量转移
相互作用体
生物物理学
黄素组
辅因子
蛋白质-蛋白质相互作用
亲和标签
生物化学
胞吐
生物正交化学
衍生工具(金融)
膜
计算生物学
细胞膜
膜蛋白
细胞
血浆蛋白结合
活体细胞成像
聚糖
蛋白质结构
法尼酰转移酶
分子信标
门控
荧光标记
紧身衣
作者
Leander Crocker,Jan Vincent V. Arafiles,Judith M. Müchler,Max Ruwolt,Kristin Kemnitz‐Hassanin,Kilian Roßmann,Christian E. Stieger,Fan Liu,Nataliya Archipowa,Roger Jan Kutta,Christian P. R. Hackenberger
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2025-09-17
卷期号:17 (12): 1928-1940
被引量:11
标识
DOI:10.1038/s41557-025-01931-8
摘要
Photocatalytic proximity labelling has emerged as a powerful tool to resolve a variety of biomolecular and cellular interactions. Although the use of high-resolution probes, such as diazirines, enables cell-surface protein labelling with nanometre precision, intracellular applications are limited by either the intrinsic toxicity of metal-based photocatalysts or by the lower resolution when long-lived reactive intermediates are used. Here we describe the discovery, characterization and application of an organic flavin cofactor derivative, deazaflavin, that activates diazirine to generate carbenes via triplet energy transfer and offers excellent biocompatibility. We demonstrate deazaflavin-diazirine energy-transfer labelling (DarT labelling) for cell surfaceome mapping and, most importantly, for intracellular interactome mapping as exemplified for cell-penetrating peptides. We successfully map the localization of linear and cyclic polyarginine cell-penetrating peptides, identifying putative membrane interactors. Furthermore, we show the applicability of DarT labelling over an extended time period by mapping the intracellular trafficking of a stable cyclic derivative to reveal its eventual exocytosis from the cell. We anticipate that DarT labelling could be used to profile intracellular dynamics across diverse biological systems with high spatio-temporal control.
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