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CPEB1 or CPEB1 (T171A, S177A) interacting proteome analysis on C2C12 cells

ABSTRACT: CPEB1 regulates cellular function by post-transcriptionally controlling its targeted transcripts' translation. After bound to CPEs, CPEB1 recruits cytoplasmic poly (A) polymerase GLD2 to elongate the poly (A) tail for the maintenance of mRNA stability. The stability of mRNA is positively correlated with translational output. It is unexamined whether CPEB1 interacts with translation machinery to regulation translation. Previous reports demonstrate that phosphorylation is required for its regulation on translation. However, it is not well understood whether phosphorylation is essential for CPEB1 interaction with translation machinery or not. Here, we performed mass spectrometry on C2 cells transfected with CPEB1-mVenus or CPEB1 (T171A, S177A)-mVenus after IgG or mVenus antibody immunoprecipitation. After analysis, we identify CPEB1 interacting proteins and the phosphorylation dependent interacting proteins such as ribosomal proteins. Thus, our data suggest that CPEB1 regulate translation by interacting with translation machinery in a phosphorylation dependent manner.

INSTRUMENT(S): timsTOF Pro

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Myoblast, Cell Culture

SUBMITTER: Tom Cheung

LAB HEAD: Tom H. Cheung

PROVIDER: PXD020822 | Pride | 2021-11-04

REPOSITORIES: Pride

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			Action	DRS
	CPEB1-1-IgG_Slot2-14_1_1110.d.zip	Other
	CPEB1-1-IgG_Slot2-14_1_1110.mgf	Mgf
	CPEB1-1-IgG_Slot2-14_1_1110.mzid.gz	Mzid
	CPEB1-1-mVenus-Ab_Slot2-16_1_1113.d.zip	Other
	CPEB1-1-mVenus-Ab_Slot2-16_1_1113.mgf	Mgf

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