Proteomics

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Genetically encoded photocatalytic protein labeling enables spatially-resolved profiling of intracellular proteome


ABSTRACT: Mapping the subcellular organization of proteins is crucial for understanding their biological functions. Herein, we report a reactive oxygen species induced protein labeling and identification (RinID) method for profiling subcellular proteome in the context of living cells. Our method capitalizes on a genetically encoded photocatalyst, miniSOG, to locally generate singlet oxygen that reacts with proximal proteins. Labeled proteins are conjugated in situ with an exogenously supplied nucleophilic probe, which serves as a functional handle for subsequent affinity enrichment and mass spectrometry-based protein identification. From a panel of nucleophilic compounds, we identify biotin-conjugated aniline and propargyl amine as highly reactive probes. As a demonstration of the spatial specificity and depth of coverage in mammalian cells, we apply RinID in the mitochondrial matrix, capturing 394 mitochondrial proteins with 97% specificity. We further demonstrate the broad applicability of RinID in various subcellular compartments, including the nucleus and the endoplasmic reticulum.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Kidney

SUBMITTER: Zheng Fu  

LAB HEAD: Peng Zou

PROVIDER: PXD034532 | Pride | 2023-07-20

REPOSITORIES: Pride

Dataset's files

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BSA_in_vitro_labeling.raw Raw
ERM_no_BL_rep1_1_5.raw Raw
ERM_no_BL_rep1_2_6.raw Raw
ERM_no_BL_rep1_3_7.raw Raw
ERM_no_BL_rep1_4_8.raw Raw
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Publications

Genetically encoded photocatalytic protein labeling enables spatially-resolved profiling of intracellular proteome.

Zheng Fu F   Yu Chenxin C   Zhou Xinyue X   Zou Peng P  

Nature communications 20230523 1


Mapping the subcellular organization of proteins is crucial for understanding their biological functions. Herein, we report a reactive oxygen species induced protein labeling and identification (RinID) method for profiling subcellular proteome in the context of living cells. Our method capitalizes on a genetically encoded photocatalyst, miniSOG, to locally generate singlet oxygen that reacts with proximal proteins. Labeled proteins are conjugated in situ with an exogenously supplied nucleophilic  ...[more]

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