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BioID-proximity labeling of GATAD1 variants

ABSTRACT: To gain insights into the interactome of wild-type (WT) and S102P mutant GATAD1, we utilized the BioID method, which enables the study of protein-protein interactions. Specifically, we performed BioID proximity labeling experiments in stable Flp-In cells expressing different GATAD1 variants fused to BirA*_FLAG. These variants included BirA*_FLAG_GATAD1-WT, BirA*_FLAG_GATAD1-S102P, BirA*_FLAG_GATAD1-S102D, and BirA*_FLAG_GATAD1-S102A. By employing this approach, we aimed to characterize the protein interactors associated with these GATAD1 variants and gain insights into the functional consequences of the S102P mutation.

INSTRUMENT(S): Orbitrap Exploris 480

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Trendelina Rrustemi

LAB HEAD: Matthias Selbach

PROVIDER: PXD043789 | Pride | 2024-02-15

REPOSITORIES: Pride

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			Action	DRS
	Rowlf_20220729_TR_HS_BioID_AspMut_ProMut_6f.raw	Raw
	Rowlf_20220729_TR_HS_BioID_AspMut_ProMut_6r.raw	Raw
	Rowlf_20220729_TR_HS_BioID_WT_AlaMut_5f.raw	Raw
	Rowlf_20220729_TR_HS_BioID_WT_Ala_Mut_5r.raw	Raw
	Rowlf_20220729_TR_HS_BioID_WT_AspMut_3f.raw	Raw

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