Proteomics

Dataset Information

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Total Synthesis and Target Identification of Marine Cyclopiane Diterpenes


ABSTRACT: We proceeded to competitive chemoproteomic profiling with conidiogenone C probe in LPS-stimulated RAW264.7 cell lysates. The lysis was then reacted with azide-biotin, and after enrichment and digestion, the peptides were labeled as “light, “medium” or “heavy” by dimethyl labeling. The labeled proteins were identified and quantified by LC-MS/MS analysis.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Cell Culture, Macrophage

SUBMITTER: shan jiang  

LAB HEAD: Houhua Li

PROVIDER: PXD047981 | Pride | 2025-05-06

REPOSITORIES: Pride

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Publications

Total synthesis and target identification of marine cyclopiane diterpenes.

Li Tian T   Jiang Shan S   Dai Yuanhao Y   Wu Xia X   Guo Huihui H   Shi Liang L   Sang Xueli X   Ren Li L   Wang Jie J   Shi Lili L   Zhou Wenming W   Li Houhua H   Hao Hong-Dong HD  

Nature communications 20241230 1


Marine cyclopianes are a family of diterpenoid with novel carbon skeleton and diverse biological activities. Herein, we report our synthetic and chemical proteomics studies of cyclopiane diterpenes which culminate in the asymmetric total synthesis of conidiogenones C, K and 12β-hydroxy conidiogenone C, and identification of Immunity-related GTPase family M protein 1 (IRGM1) as a cellular target. Our asymmetric synthesis commences from Wieland-Miescher ketone and features a sequential intramolecu  ...[more]

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