HiPLA: High-throughput imaging proximity ligation assay.


Journal

Methods (San Diego, Calif.)
ISSN: 1095-9130
Titre abrégé: Methods
Pays: United States
ID NLM: 9426302

Informations de publication

Date de publication:
15 03 2019
Historique:
received: 12 07 2018
revised: 29 10 2018
accepted: 06 11 2018
pubmed: 13 11 2018
medline: 22 11 2019
entrez: 13 11 2018
Statut: ppublish

Résumé

Protein-protein interactions are essential for cellular structure and function. To delineate how the intricate assembly of protein interactions contribute to cellular processes in health and disease, new methodologies that are both highly sensitive and can be applied at large scale are needed. Here, we develop HiPLA (high-throughput imaging proximity ligation assay), a method that employs the well-established antibody-based proximity ligation assay in a high-throughput imaging screening format as a novel means to systematically visualize protein interactomes. Using HiPLA with a library of antibodies targeting nuclear proteins, we probe the interaction of 60 proteins and associated post-translational modifications (PTMs) with the nuclear lamina in a model of the premature aging disorder Hutchinson-Gilford progeria syndrome (HGPS). We identify a subset of proteins that differentially interact with the nuclear lamina in HGPS. Using HiPLA in combination with quantitative indirect immunofluorescence, we find that the majority of differential interactions are accompanied by corresponding changes in expression of the interacting protein. Taken together, HiPLA offers a novel approach to probe cellular protein-protein interaction at a large scale and reveals mechanistic insights into the assembly of protein complexes.

Identifiants

pubmed: 30419336
pii: S1046-2023(18)30114-2
doi: 10.1016/j.ymeth.2018.11.004
pmc: PMC6401276
mid: NIHMS1512202
pii:
doi:

Substances chimiques

Lamin Type A 0
Protein Precursors 0

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

80-87

Subventions

Organisme : Intramural NIH HHS
ID : ZIA BC010309-19
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA BC010309-20
Pays : United States

Informations de copyright

Published by Elsevier Inc.

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Auteurs

Leonid A Serebryannyy (LA)

Cell Biology of Genomes Group, National Cancer Institute, NIH, Building 41, 41 Library Drive, Bethesda, MD 20892, USA.

Tom Misteli (T)

Cell Biology of Genomes Group, National Cancer Institute, NIH, Building 41, 41 Library Drive, Bethesda, MD 20892, USA. Electronic address: mistelit@mail.nih.gov.

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Classifications MeSH