A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape

Philipp Hubel; Christian Urban; Valter Bergant; William M Schneider; Barbara Knauer; Alexey Stukalov; Pietro Scaturro; Angelika Mann; Linda Brunotte; Heinrich H Hoffmann; John W Schoggins; Martin Schwemmle; Matthias Mann; Charles M Rice; Andreas Pichlmair

doi:10.1038/s41590-019-0323-3

A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape

Philipp Hubel, Christian Urban, Valter Bergant, William M Schneider, Barbara Knauer, Alexey Stukalov, Pietro Scaturro, Angelika Mann, Linda Brunotte, Heinrich H Hoffmann, John W Schoggins, Martin Schwemmle, Matthias Mann, Charles M Rice, Andreas Pichlmair

37 Citationer (Scopus)

Abstract

Interferon-stimulated genes (ISGs) form the backbone of the innate immune system and are important for limiting intra- and intercellular viral replication and spread. We conducted a mass-spectrometry-based survey to understand the fundamental organization of the innate immune system and to explore the molecular functions of individual ISGs. We identified interactions between 104 ISGs and 1,401 cellular binding partners engaging in 2,734 high-confidence interactions. 90% of these interactions are unreported so far, and our survey therefore illuminates a far wider activity spectrum of ISGs than is currently known. Integration of the resulting ISG-interaction network with published datasets and functional studies allowed us to identify regulators of immunity and processes related to the immune system. Given the extraordinary robustness of the innate immune system, this ISG network may serve as a blueprint for therapeutic targeting of cellular systems to efficiently fight viral infections.

Originalsprog	Engelsk
Tidsskrift	Nature Immunology
ISSN	1529-2908
DOI	https://doi.org/10.1038/s41590-019-0323-3
Status	Udgivet - 1 apr. 2019
Udgivet eksternt	Ja

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10.1038/s41590-019-0323-3

Citationsformater

Hubel, P., Urban, C., Bergant, V., Schneider, W. M., Knauer, B., Stukalov, A., Scaturro, P., Mann, A., Brunotte, L., Hoffmann, H. H., Schoggins, J. W., Schwemmle, M., Mann, M., Rice, C. M., & Pichlmair, A. (2019). A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape. Nature Immunology. https://doi.org/10.1038/s41590-019-0323-3

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abstract = "Interferon-stimulated genes (ISGs) form the backbone of the innate immune system and are important for limiting intra- and intercellular viral replication and spread. We conducted a mass-spectrometry-based survey to understand the fundamental organization of the innate immune system and to explore the molecular functions of individual ISGs. We identified interactions between 104 ISGs and 1,401 cellular binding partners engaging in 2,734 high-confidence interactions. 90% of these interactions are unreported so far, and our survey therefore illuminates a far wider activity spectrum of ISGs than is currently known. Integration of the resulting ISG-interaction network with published datasets and functional studies allowed us to identify regulators of immunity and processes related to the immune system. Given the extraordinary robustness of the innate immune system, this ISG network may serve as a blueprint for therapeutic targeting of cellular systems to efficiently fight viral infections.",

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T1 - A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape

AU - Hubel, Philipp

AU - Urban, Christian

AU - Bergant, Valter

AU - Schneider, William M

AU - Knauer, Barbara

AU - Stukalov, Alexey

AU - Scaturro, Pietro

AU - Mann, Angelika

AU - Brunotte, Linda

AU - Hoffmann, Heinrich H

AU - Schoggins, John W

AU - Schwemmle, Martin

AU - Mann, Matthias

AU - Rice, Charles M

AU - Pichlmair, Andreas

PY - 2019/4/1

Y1 - 2019/4/1

N2 - Interferon-stimulated genes (ISGs) form the backbone of the innate immune system and are important for limiting intra- and intercellular viral replication and spread. We conducted a mass-spectrometry-based survey to understand the fundamental organization of the innate immune system and to explore the molecular functions of individual ISGs. We identified interactions between 104 ISGs and 1,401 cellular binding partners engaging in 2,734 high-confidence interactions. 90% of these interactions are unreported so far, and our survey therefore illuminates a far wider activity spectrum of ISGs than is currently known. Integration of the resulting ISG-interaction network with published datasets and functional studies allowed us to identify regulators of immunity and processes related to the immune system. Given the extraordinary robustness of the innate immune system, this ISG network may serve as a blueprint for therapeutic targeting of cellular systems to efficiently fight viral infections.

AB - Interferon-stimulated genes (ISGs) form the backbone of the innate immune system and are important for limiting intra- and intercellular viral replication and spread. We conducted a mass-spectrometry-based survey to understand the fundamental organization of the innate immune system and to explore the molecular functions of individual ISGs. We identified interactions between 104 ISGs and 1,401 cellular binding partners engaging in 2,734 high-confidence interactions. 90% of these interactions are unreported so far, and our survey therefore illuminates a far wider activity spectrum of ISGs than is currently known. Integration of the resulting ISG-interaction network with published datasets and functional studies allowed us to identify regulators of immunity and processes related to the immune system. Given the extraordinary robustness of the innate immune system, this ISG network may serve as a blueprint for therapeutic targeting of cellular systems to efficiently fight viral infections.

U2 - 10.1038/s41590-019-0323-3

DO - 10.1038/s41590-019-0323-3

M3 - Journal article

C2 - 30833792

SN - 1529-2908

JO - Nature Immunology

JF - Nature Immunology

ER -

A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape

Abstract

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