Proteomics

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A method for spatially and temporally resolved protein network interrogation in living cells


ABSTRACT: Cells operate through protein interaction networks organized in space and in time, but current methods to interrogate such biology typically resolve only one of these dimensions. Here, we describe a method to resolve both dimensions simultaneously using proximity labeling mediated by engineered ascorbic acid peroxidase (APEX). APEX has been used to label organelle proteomes with high temporal resolution, but its spatial resolution is generally thought to be limited because of its larger labeling radius. We describe an analytical pipeline, based on quantitative proteomics using spatial references, which overcomes this barrier. As proof-of-principle, we apply the methodology to interrogate protein interaction networks of G protein coupled receptors both temporally and spatially. Using this approach, we identify known binding partners as well as novel receptor regulators. Validating the methodology as a discovery tool, we demonstrate that two of these components drive ubiquitin-linked down-regulation of opioid receptors.

INSTRUMENT(S): Orbitrap Fusion, LTQ Orbitrap Elite

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

SUBMITTER: Ruth Huttenhain  

PROVIDER: MSV000084857 | MassIVE | Wed Jan 29 16:56:00 GMT 2020

SECONDARY ACCESSION(S): PXD005758

REPOSITORIES: MassIVE

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Publications

An Approach to Spatiotemporally Resolve Protein Interaction Networks in Living Cells.

Lobingier Braden T BT   Hüttenhain Ruth R   Eichel Kelsie K   Miller Kenneth B KB   Ting Alice Y AY   von Zastrow Mark M   Krogan Nevan J NJ  

Cell 20170401 2


Cells operate through protein interaction networks organized in space and time. Here, we describe an approach to resolve both dimensions simultaneously by using proximity labeling mediated by engineered ascorbic acid peroxidase (APEX). APEX has been used to capture entire organelle proteomes with high temporal resolution, but its breadth of labeling is generally thought to preclude the higher spatial resolution necessary to interrogate specific protein networks. We provide a solution to this pro  ...[more]

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