Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling

Methods to identify protein interaction networks often suffer from poor spatiotemporal resolution. Here the authors present a light-activated proximity labeling method where the protein of interest is fused to the photosensitizer protein miniSOG, allowing temporally resolved labeling of interactors.

Bibliographic Details
Main Authors: Yansheng Zhai, Xiaoyan Huang, Keren Zhang, Yuchen Huang, Yanlong Jiang, Jingwei Cui, Zhe Zhang, Cookson K. C. Chiu, Weiye Zhong, Gang Li
Format: Article
Language:English
Published: Nature Portfolio 2022-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-32689-z
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author Yansheng Zhai
Xiaoyan Huang
Keren Zhang
Yuchen Huang
Yanlong Jiang
Jingwei Cui
Zhe Zhang
Cookson K. C. Chiu
Weiye Zhong
Gang Li
author_facet Yansheng Zhai
Xiaoyan Huang
Keren Zhang
Yuchen Huang
Yanlong Jiang
Jingwei Cui
Zhe Zhang
Cookson K. C. Chiu
Weiye Zhong
Gang Li
author_sort Yansheng Zhai
collection DOAJ
description Methods to identify protein interaction networks often suffer from poor spatiotemporal resolution. Here the authors present a light-activated proximity labeling method where the protein of interest is fused to the photosensitizer protein miniSOG, allowing temporally resolved labeling of interactors.
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spelling doaj.art-02955cce232c437cb11554572b2a401a2022-12-22T02:34:40ZengNature PortfolioNature Communications2041-17232022-08-0113111210.1038/s41467-022-32689-zSpatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labelingYansheng Zhai0Xiaoyan Huang1Keren Zhang2Yuchen Huang3Yanlong Jiang4Jingwei Cui5Zhe Zhang6Cookson K. C. Chiu7Weiye Zhong8Gang Li9Institute of Systems and Physical Biology, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryDepartment of Chemistry, UF Scripps Biomedical ResearchInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryMulti-omics Mass Spectrometry Core, Office of Core Facility, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryInstitute of Systems and Physical Biology, Shenzhen Bay LaboratoryMethods to identify protein interaction networks often suffer from poor spatiotemporal resolution. Here the authors present a light-activated proximity labeling method where the protein of interest is fused to the photosensitizer protein miniSOG, allowing temporally resolved labeling of interactors.https://doi.org/10.1038/s41467-022-32689-z
spellingShingle Yansheng Zhai
Xiaoyan Huang
Keren Zhang
Yuchen Huang
Yanlong Jiang
Jingwei Cui
Zhe Zhang
Cookson K. C. Chiu
Weiye Zhong
Gang Li
Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
Nature Communications
title Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
title_full Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
title_fullStr Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
title_full_unstemmed Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
title_short Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling
title_sort spatiotemporal resolved protein networks profiling with photoactivation dependent proximity labeling
url https://doi.org/10.1038/s41467-022-32689-z
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