A Cell-Permeable Photosensitizer for Selective Proximity Labeling and Crosslinking of Aggregated Proteome.
Huan FengQun ZhaoNan ZhaoZhen LiangYanan HuangXin ZhangLihua ZhangLiu YuPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Intracellular proteome aggregation is a ubiquitous disease hallmark with its composition associated with pathogenicity. Herein, this work reports on a cell-permeable photosensitizer (P8, Rose Bengal derivative) for selective photo induced proximity labeling and crosslinking of cellular aggregated proteome. Rose Bengal is identified out of common photosensitizer scaffolds for its unique intrinsic binding affinity to various protein aggregates driven by the hydrophobic effect. Further acetylation permeabilizes Rose Bengal to selectively image, label, and crosslink aggregated proteome in live stressed cells. A combination of photo-chemical, tandem mass spectrometry, and protein biochemistry characterizations reveals the complexity in photosensitizing pathways (both Type I & II), modification sites and labeling mechanisms. The diverse labeling sites and reaction types result in highly effective enrichment and identification of aggregated proteome. Finally, aggregated proteomics and interaction analyses thereby reveal extensive entangling of proteostasis network components mediated by HSP70 chaperone (HSPA1B) and active participation of autophagy pathway in combating proteasome inhibition. Overall, this work exemplifies the first photo induced proximity labeling and crosslinking method (namely AggID) to profile intracellular aggregated proteome and analyze its interactions.
Keyphrases
- photodynamic therapy
- tandem mass spectrometry
- single cell
- heat shock protein
- high glucose
- cell therapy
- cell death
- high performance liquid chromatography
- induced apoptosis
- mass spectrometry
- oxidative stress
- drug induced
- diabetic rats
- gene expression
- deep learning
- high resolution
- physical activity
- protein protein
- amino acid
- genome wide
- endothelial cells
- reactive oxygen species
- staphylococcus aureus
- escherichia coli
- ionic liquid
- bone marrow
- pseudomonas aeruginosa
- dna methylation
- solid phase extraction
- electron transfer