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  1. Article ; Online: PIGNON: a protein-protein interaction-guided functional enrichment analysis for quantitative proteomics.

    Nadeau, Rachel / Byvsheva, Anastasiia / Lavallée-Adam, Mathieu

    BMC bioinformatics

    2021  Volume 22, Issue 1, Page(s) 302

    Abstract: Background: Quantitative proteomics studies are often used to detect proteins that are differentially expressed across different experimental conditions. Functional enrichment analyses are then typically used to detect annotations, such as biological ... ...

    Abstract Background: Quantitative proteomics studies are often used to detect proteins that are differentially expressed across different experimental conditions. Functional enrichment analyses are then typically used to detect annotations, such as biological processes that are significantly enriched among such differentially expressed proteins to provide insights into the molecular impacts of the studied conditions. While common, this analytical pipeline often heavily relies on arbitrary thresholds of significance. However, a functional annotation may be dysregulated in a given experimental condition, while none, or very few of its proteins may be individually considered to be significantly differentially expressed. Such an annotation would therefore be missed by standard approaches.
    Results: Herein, we propose a novel graph theory-based method, PIGNON, for the detection of differentially expressed functional annotations in different conditions. PIGNON does not assess the statistical significance of the differential expression of individual proteins, but rather maps protein differential expression levels onto a protein-protein interaction network and measures the clustering of proteins from a given functional annotation within the network. This process allows the detection of functional annotations for which the proteins are differentially expressed and grouped in the network. A Monte-Carlo sampling approach is used to assess the clustering significance of proteins in an expression-weighted network. When applied to a quantitative proteomics analysis of different molecular subtypes of breast cancer, PIGNON detects Gene Ontology terms that are both significantly clustered in a protein-protein interaction network and differentially expressed across different breast cancer subtypes. PIGNON identified functional annotations that are dysregulated and clustered within the network between the HER2+, triple negative and hormone receptor positive subtypes. We show that PIGNON's results are complementary to those of state-of-the-art functional enrichment analyses and that it highlights functional annotations missed by standard approaches. Furthermore, PIGNON detects functional annotations that have been previously associated with specific breast cancer subtypes.
    Conclusion: PIGNON provides an alternative to functional enrichment analyses and a more comprehensive characterization of quantitative datasets. Hence, it contributes to yielding a better understanding of dysregulated functions and processes in biological samples under different experimental conditions.
    MeSH term(s) Biological Phenomena ; Cluster Analysis ; Humans ; Protein Interaction Maps ; Proteins ; Proteomics
    Chemical Substances Proteins
    Language English
    Publishing date 2021-06-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041484-5
    ISSN 1471-2105 ; 1471-2105
    ISSN (online) 1471-2105
    ISSN 1471-2105
    DOI 10.1186/s12859-021-04042-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Proteomics characterization of mitochondrial-derived vesicles under oxidative stress.

    Vasam, Goutham / Nadeau, Rachel / Cadete, Virgilio J J / Lavallée-Adam, Mathieu / Menzies, Keir J / Burelle, Yan

    FASEB journal : official publication of the Federation of American Societies for Experimental Biology

    2021  Volume 35, Issue 4, Page(s) e21278

    Abstract: Mitochondria share attributes of vesicular transport with their bacterial ancestors given their ability to form mitochondrial-derived vesicles (MDVs). MDVs are involved in mitochondrial quality control and their formation is enhanced with stress and may, ...

    Abstract Mitochondria share attributes of vesicular transport with their bacterial ancestors given their ability to form mitochondrial-derived vesicles (MDVs). MDVs are involved in mitochondrial quality control and their formation is enhanced with stress and may, therefore, play a potential role in mitochondrial-cellular communication. However, MDV proteomic cargo has remained mostly undefined. In this study, we strategically used an in vitro MDV budding/reconstitution assay on cardiac mitochondria, followed by graded oxidative stress, to identify and characterize the MDV proteome. Our results confirmed previously identified cardiac MDV markers, while also revealing a complete map of the MDV proteome, paving the way to a better understanding of the role of MDVs. The oxidative stress vulnerability of proteins directed the cargo loading of MDVs, which was enhanced by antimycin A (Ant-A). Among OXPHOS complexes, complexes III and V were found to be Ant-A-sensitive. Proteins from metabolic pathways such as the TCA cycle and fatty acid metabolism, along with Fe-S cluster, antioxidant response proteins, and autophagy were also found to be Ant-A sensitive. Intriguingly, proteins containing hyper-reactive cysteine residues, metabolic redox switches, including professional redox enzymes and those that mediate iron metabolism, were found to be components of MDV cargo with Ant-A sensitivity. Last, we revealed a possible contribution of MDVs to the formation of extracellular vesicles, which may indicate mitochondrial stress. In conclusion, our study provides an MDV proteomics signature that delineates MDV cargo selectivity and hints at the potential for MDVs and their novel protein cargo to serve as vital biomarkers during mitochondrial stress and related pathologies.
    MeSH term(s) Animals ; Cell Line ; Gene Expression Regulation ; Mitochondria, Heart/physiology ; Mitochondrial Proteins/genetics ; Mitochondrial Proteins/metabolism ; Myoblasts ; Oxidative Stress ; Proteomics ; Rats ; Transport Vesicles/physiology
    Chemical Substances Mitochondrial Proteins
    Language English
    Publishing date 2021-03-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639186-2
    ISSN 1530-6860 ; 0892-6638
    ISSN (online) 1530-6860
    ISSN 0892-6638
    DOI 10.1096/fj.202002151R
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Computational Identification of Human Biological Processes and Protein Sequence Motifs Putatively Targeted by SARS-CoV-2 Proteins Using Protein-Protein Interaction Networks.

    Nadeau, Rachel / Shahryari Fard, Soroush / Scheer, Amit / Hashimoto-Roth, Emily / Nygard, Dallas / Abramchuk, Iryna / Chung, Yun-En / Bennett, Steffany A L / Lavallée-Adam, Mathieu

    Journal of proteome research

    2020  Volume 19, Issue 11, Page(s) 4553–4566

    Abstract: While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a ...

    Abstract While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a better understanding of the mechanisms exploited by the virus and enable the identification of potential drug targets. We therefore performed an in-depth computational analysis of the interactome of SARS-CoV-2 and human proteins in infected HEK 293 cells published by Gordon et al. (
    MeSH term(s) Algorithms ; Amino Acid Motifs ; Betacoronavirus/chemistry ; Betacoronavirus/metabolism ; Betacoronavirus/pathogenicity ; COVID-19 ; Cluster Analysis ; Coronavirus Infections/metabolism ; Coronavirus Infections/virology ; Gene Ontology ; HEK293 Cells ; Host-Pathogen Interactions/genetics ; Humans ; Molecular Sequence Annotation ; Pandemics ; Pneumonia, Viral/metabolism ; Pneumonia, Viral/virology ; Protein Binding ; Protein Interaction Maps/genetics ; Protein Interaction Maps/physiology ; Proteins/chemistry ; Proteins/classification ; Proteins/genetics ; Proteins/metabolism ; SARS-CoV-2 ; Viral Proteins/chemistry ; Viral Proteins/genetics ; Viral Proteins/metabolism
    Chemical Substances Proteins ; Viral Proteins
    Keywords covid19
    Language English
    Publishing date 2020-10-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.0c00422
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Computational identification of human biological processes and protein sequence motifs putatively targeted by SARS-CoV-2 proteins using protein-protein interaction networks

    Nadeau, Rachel / Fard, Soroush Shahryari / Scheer, Amit / Roth, Emily / Nygard, Dallas / Abramchuk, Iryna / Chung, Yun-En / Bennett, Steffany A. L. / Lavallée-Adam, Mathieu

    bioRxiv

    Abstract: While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a ...

    Abstract While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a better understanding of the mechanisms exploited by the virus and enable the identification of potential drug targets. We therefore performed an in-depth computational analysis of the interactome of SARS-CoV-2 and human proteins in infected HEK293 cells published by Gordon et al. to reveal processes that are potentially affected by the virus and putative protein binding sites. Specifically, we performed a set of network-based functional and sequence motif enrichment analyses on SARS-CoV-2-interacting human proteins and on a PPI network generated by supplementing viral-host PPIs with known interactions. Using a novel implementation of our GoNet algorithm, we identified 329 Gene Ontology terms for which the SARS-CoV-2-interacting human proteins are significantly clustered in the network. Furthermore, we present a novel protein sequence motif discovery approach, LESMoN-Pro, that identified 9 amino acid motifs for which the associated proteins are clustered in the network. Together, these results provide insights into the processes and sequence motifs that are putatively implicated in SARS-CoV-2 infection and could lead to potential therapeutic targets.
    Keywords covid19
    Publisher BioRxiv; WHO
    Document type Article ; Online
    DOI 10.1101/2020.09.29.318931
    Database COVID19

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  5. Article: Computational Identification of Human Biological Processes and Protein Sequence Motifs Putatively Targeted by SARS-CoV-2 Proteins Using Protein-Protein Interaction Networks

    Nadeau, Rachel / Shahryari Fard, Soroush / Scheer, Amit / Hashimoto-Roth, Emily / Nygard, Dallas / Abramchuk, Iryna / Chung, Yun-En / Bennett, Steffany A L / Lavallée-Adam, Mathieu

    J Proteome Res

    Abstract: While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a ...

    Abstract While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a better understanding of the mechanisms exploited by the virus and enable the identification of potential drug targets. We therefore performed an in-depth computational analysis of the interactome of SARS-CoV-2 and human proteins in infected HEK 293 cells published by Gordon et al. (Nature 2020, 583, 459-468) to reveal processes that are potentially affected by the virus and putative protein binding sites. Specifically, we performed a set of network-based functional and sequence motif enrichment analyses on SARS-CoV-2-interacting human proteins and on PPI networks generated by supplementing viral-host PPIs with known interactions. Using a novel implementation of our GoNet algorithm, we identified 329 Gene Ontology terms for which the SARS-CoV-2-interacting human proteins are significantly clustered in PPI networks. Furthermore, we present a novel protein sequence motif discovery approach, LESMoN-Pro, that identified 9 amino acid motifs for which the associated proteins are clustered in PPI networks. Together, these results provide insights into the processes and sequence motifs that are putatively implicated in SARS-CoV-2 infection and could lead to potential therapeutic targets.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #889122
    Database COVID19

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  6. Article ; Online: Computational identification of human biological processes and protein sequence motifs putatively targeted by SARS-CoV-2 proteins using protein-protein interaction networks

    Nadeau, Rachel / Shahryari Fard, Soroush / Scheer, Amit / Hashimoto-Roth, Emily / Nygard, Dallas / Abramchuk, Iryna / Chung, Yun-En / Bennett, Steffany A. L. / Lavallee-Adam, Mathieu

    bioRxiv

    Abstract: While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a ...

    Abstract While the COVID-19 pandemic is causing important loss of life, knowledge of the effects of the causative SARS-CoV-2 virus on human cells is currently limited. Investigating protein-protein interactions (PPIs) between viral and host proteins can provide a better understanding of the mechanisms exploited by the virus and enable the identification of potential drug targets. We therefore performed an in-depth computational analysis of the interactome of SARS-CoV-2 and human proteins in infected HEK293 cells published by Gordon et al. to reveal processes that are potentially affected by the virus and putative protein binding sites. Specifically, we performed a set of network-based functional and sequence motif enrichment analyses on SARS-CoV-2-interacting human proteins and on a PPI network generated by supplementing viral-host PPIs with known interactions. Using a novel implementation of our GoNet algorithm, we identified 329 Gene Ontology terms for which the SARS-CoV-2-interacting human proteins are significantly clustered in the network. Furthermore, we present a novel protein sequence motif discovery approach, LESMoN-Pro, that identified 9 amino acid motifs for which the associated proteins are clustered in the network. Together, these results provide insights into the processes and sequence motifs that are putatively implicated in SARS-CoV-2 infection and could lead to potential therapeutic targets.
    Keywords covid19
    Language English
    Publishing date 2020-09-30
    Publisher Cold Spring Harbor Laboratory
    Document type Article ; Online
    DOI 10.1101/2020.09.29.318931
    Database COVID19

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  7. Article ; Online: Computational Identification of Human Biological Processes and Protein Sequence Motifs Putatively Targeted by SARS-CoV-2 Proteins Using Protein–Protein Interaction Networks

    Nadeau, Rachel / Shahryari Fard, Soroush / Scheer, Amit / Hashimoto-Roth, Emily / Nygard, Dallas / Abramchuk, Iryna / Chung, Yun-En / Bennett, Steffany A. L. / Lavallée-Adam, Mathieu

    Journal of Proteome Research

    2020  Volume 19, Issue 11, Page(s) 4553–4566

    Keywords Biochemistry ; General Chemistry ; covid19
    Language English
    Publisher American Chemical Society (ACS)
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2078618-9
    ISSN 1535-3893
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.0c00422
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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