Proteomics

Dataset Information

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Affinity Purification Mass Spectrometry of protein protein interactors with alternatively-spliced Uromodulin


ABSTRACT: We identified an alternatively spliced UMOD which is uniquely localized intracellularly. This intracellular isoform enhanced mitochondrial function. To understand its molecular mechanism, we performed affinity-purification coupled to mass spectrometry using MDCK cell lysate expressing UMOD variant. We prepared MDCK cells which express mock (negative control), wild-type human UMOD or alternatively spliced human UMOD. UMOD was isolated by Immunoprecipitation and interacting proteins were identified by mass spectrometry proteomics analysis.

INSTRUMENT(S): Orbitrap Exploris 480

ORGANISM(S): Canis Lupus Familiaris (ncbitaxon:9615) Homo Sapiens (ncbitaxon:9606)

SUBMITTER: Tarek M. El-Achkar   Amber L. Mosley  

PROVIDER: MSV000094329 | MassIVE | Fri Mar 15 12:52:00 GMT 2024

SECONDARY ACCESSION(S): PXD050667

REPOSITORIES: MassIVE

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Publications


In the kidney, cells of thick ascending limb of the loop of Henle (TAL) are resistant to ischemic injury, despite high energy demands. This adaptive metabolic response is not fully understood even though the integrity of TAL cells is essential for recovery from acute kidney injury (AKI). TAL cells uniquely express uromodulin, the most abundant protein secreted in healthy urine. Here, we demonstrate that alternative splicing generates a conserved intracellular isoform of uromodulin, which contrib  ...[more]

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