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Updated: Sep 17, 2025

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells
Published on: June 30, 2018
Genetically Encoded Near-Infrared Photocatalysis for Proximity Labeling of Subcellular Proteome
Tianyu Ren1, Jinsaibo Gong2, Fu Zheng2
1State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.
Abstract:
The spatial organization of proteins in eukaryotic cells plays essential roles in cellular functions. Genetically encoded proximity labeling methods offer spatially resolved and proteome-wide mapping of protein localization, yet existing techniques are limited to blue light activation, which has limited tissue penetration and causes a high cellular background. Here, we report the development of a near-infrared photocatalytic proximity labeling method, FLAPP, based on the engineered fluorogen-activating protein dL5**. Upon binding to the fluorogenic iodinated malachite green, the complex can efficiently absorb near-IR light to produce singlet oxygen that reacts in situ with nearby histidine residues. Unlike most existing near-infrared light-activated proximity labeling techniques that rely on antibody-dependent membrane targeting, FLAPP is a genetically encoded near-infrared light-activated proximity labeling technology. We demonstrate the high spatial specificity (96%) of FLAPP in the mitochondria and nucleus. FLAPP enables the deep tissue penetration of protein labeling, underscoring its potential for live animal applications.
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