An experimentally derived confidence score for binary protein-protein interactions
Use of the protein-protein interaction reference sets reported in this issue in Venkatesan et al . to benchmark four complementary protein-protein interaction assays, followed by the training of a logistic regression model, allows the assignment of standardized confidence scores to individual protei...
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Published in | Nature methods Vol. 6; no. 1; pp. 91 - 97 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.01.2009
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1548-7091 1548-7105 |
DOI | 10.1038/nmeth.1281 |
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Abstract | Use of the protein-protein interaction reference sets reported in this issue in Venkatesan
et al
. to benchmark four complementary protein-protein interaction assays, followed by the training of a logistic regression model, allows the assignment of standardized confidence scores to individual protein-protein interactions.
Information on protein-protein interactions is of central importance for many areas of biomedical research. At present no method exists to systematically and experimentally assess the quality of individual interactions reported in interaction mapping experiments. To provide a standardized confidence-scoring method that can be applied to tens of thousands of protein interactions, we have developed an interaction tool kit consisting of four complementary, high-throughput protein interaction assays. We benchmarked these assays against positive and random reference sets consisting of well documented pairs of interacting human proteins and randomly chosen protein pairs, respectively. A logistic regression model was trained using the data from these reference sets to combine the assay outputs and calculate the probability that any newly identified interaction pair is a true biophysical interaction once it has been tested in the tool kit. This general approach will allow a systematic and empirical assignment of confidence scores to all individual protein-protein interactions in interactome networks. |
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AbstractList | Use of the protein-protein interaction reference sets reported in this issue in Venkatesan
et al
. to benchmark four complementary protein-protein interaction assays, followed by the training of a logistic regression model, allows the assignment of standardized confidence scores to individual protein-protein interactions.
Information on protein-protein interactions is of central importance for many areas of biomedical research. At present no method exists to systematically and experimentally assess the quality of individual interactions reported in interaction mapping experiments. To provide a standardized confidence-scoring method that can be applied to tens of thousands of protein interactions, we have developed an interaction tool kit consisting of four complementary, high-throughput protein interaction assays. We benchmarked these assays against positive and random reference sets consisting of well documented pairs of interacting human proteins and randomly chosen protein pairs, respectively. A logistic regression model was trained using the data from these reference sets to combine the assay outputs and calculate the probability that any newly identified interaction pair is a true biophysical interaction once it has been tested in the tool kit. This general approach will allow a systematic and empirical assignment of confidence scores to all individual protein-protein interactions in interactome networks. Information on protein-protein interactions is of central importance for many areas of biomedical research. At present no method exists to systematically and experimentally assess the quality of individual interactions reported in interaction mapping experiments. To provide a standardized confidence-scoring method that can be applied to tens of thousands of protein interactions, we have developed an interaction tool kit consisting of four complementary, high-throughput protein interaction assays. We benchmarked these assays against positive and random reference sets consisting of well documented pairs of interacting human proteins and randomly chosen protein pairs, respectively. A logistic regression model was trained using the data from these reference sets to combine the assay outputs and calculate the probability that any newly identified interaction pair is a true biophysical interaction once it has been tested in the tool kit. This general approach will allow a systematic and empirical assignment of confidence scores to all individual protein-protein interactions in interactome networks. [PUBLICATION ABSTRACT] Information on protein-protein interactions is of central importance for many areas of biomedical research. At present no method exists to systematically and experimentally assess the quality of individual interactions reported in interaction mapping experiments. To provide a standardized confidence-scoring method that can be applied to tens of thousands of protein interactions, we have developed an interaction tool kit consisting of four complementary, high-throughput protein interaction assays. We benchmarked these assays against positive and random reference sets consisting of well documented pairs of interacting human proteins and randomly chosen protein pairs, respectively. A logistic regression model was trained using the data from these reference sets to combine the assay outputs and calculate the probability that any newly identified interaction pair is a true biophysical interaction once it has been tested in the tool kit. This general approach will allow a systematic and empirical assignment of confidence scores to all individual protein-protein interactions in interactome networks. Information on protein-protein interactions is of central importance for many areas of biomedical research. Currently no method exists to systematically and experimentally assess the quality of individual interactions reported in interaction mapping experiments. To provide a standardized confidence-scoring method that can be applied to tens of thousands of protein interactions we have developed an interaction tool-kit consisting of four complementary high-throughput (HT) protein interaction assays. These assays were benchmarked against positive and random reference sets (PRS and RRS) consisting of well documented human interaction pairs and randomly chosen protein pairs, respectively. A logistic regression model was trained using the PRS/RRS data to combine the assay outputs and calculate the probability that any novel interaction pair is a true biophysical interaction once it has been tested in the tool-kit. This general approach will allow a systematic and empirical assignment of confidence scores to all individual protein-protein interactions in interactome networks. |
Audience | Academic |
Author | Cusick, Michael E Wrana, Jeffrey L Braun, Pascal Dreze, Matija Lemmens, Irma Roth, Frederick P Barrios-Rodiles, Miriam Yu, Haiyuan Roncari, Luba Vidal, Marc Murray, Ryan R Rual, Jean-François Hill, David E Sahalie, Julie M de Smet, Anne-Sophie Tasan, Murat Pawson, Tony Venkatesan, Kavitha Tavernier, Jan Vandenhaute, Jean |
AuthorAffiliation | 3 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 250 Longwood Avenue, Boston, Massachusetts 02115, USA 1 Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA 2 Department of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA 5 Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto Ontario M5G 1X5 4 Facultés Universitaires Notre-Dame de la Paix, 61 Rue de Bruxelles, 5000 Namur, Belgium 6 Department of Medical Protein Research, VIB, and Department of Biochemistry, Faculty of Medicine and Health Sciences, Ghent University, 9000 Ghent, Belgium |
AuthorAffiliation_xml | – name: 6 Department of Medical Protein Research, VIB, and Department of Biochemistry, Faculty of Medicine and Health Sciences, Ghent University, 9000 Ghent, Belgium – name: 4 Facultés Universitaires Notre-Dame de la Paix, 61 Rue de Bruxelles, 5000 Namur, Belgium – name: 1 Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA – name: 2 Department of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA – name: 3 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 250 Longwood Avenue, Boston, Massachusetts 02115, USA – name: 5 Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto Ontario M5G 1X5 |
Author_xml | – sequence: 1 givenname: Pascal surname: Braun fullname: Braun, Pascal email: pascal_braun@dfci.harvard.edu organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 2 givenname: Murat surname: Tasan fullname: Tasan, Murat organization: Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School – sequence: 3 givenname: Matija surname: Dreze fullname: Dreze, Matija organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School, Facultés Universitaires Notre-Dame de la Paix – sequence: 4 givenname: Miriam surname: Barrios-Rodiles fullname: Barrios-Rodiles, Miriam organization: Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital – sequence: 5 givenname: Irma surname: Lemmens fullname: Lemmens, Irma organization: Department of Medical Protein Research, and Department of Biochemistry, Flanders Institute for Biotechnology, Faculty of Medicine and Health Sciences, Ghent University – sequence: 6 givenname: Haiyuan surname: Yu fullname: Yu, Haiyuan organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 7 givenname: Julie M surname: Sahalie fullname: Sahalie, Julie M organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 8 givenname: Ryan R surname: Murray fullname: Murray, Ryan R organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 9 givenname: Luba surname: Roncari fullname: Roncari, Luba organization: Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital – sequence: 10 givenname: Anne-Sophie surname: de Smet fullname: de Smet, Anne-Sophie organization: Department of Medical Protein Research, and Department of Biochemistry, Flanders Institute for Biotechnology, Faculty of Medicine and Health Sciences, Ghent University – sequence: 11 givenname: Kavitha surname: Venkatesan fullname: Venkatesan, Kavitha organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School, Present addresses: Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue Cambridge MA 02139 (K.V.) and Harvard Medical School, Department of Cell Biology, 240 Longwood Avenue, Boston, Massachusetts 02115, USA (J.-F.R.) – sequence: 12 givenname: Jean-François surname: Rual fullname: Rual, Jean-François organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School, Present addresses: Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue Cambridge MA 02139 (K.V.) and Harvard Medical School, Department of Cell Biology, 240 Longwood Avenue, Boston, Massachusetts 02115, USA (J.-F.R.) – sequence: 13 givenname: Jean surname: Vandenhaute fullname: Vandenhaute, Jean organization: Facultés Universitaires Notre-Dame de la Paix – sequence: 14 givenname: Michael E surname: Cusick fullname: Cusick, Michael E organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 15 givenname: Tony surname: Pawson fullname: Pawson, Tony organization: Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital – sequence: 16 givenname: David E surname: Hill fullname: Hill, David E organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School – sequence: 17 givenname: Jan surname: Tavernier fullname: Tavernier, Jan email: jan.tavernier@ugent.be organization: Department of Medical Protein Research, and Department of Biochemistry, Flanders Institute for Biotechnology, Faculty of Medicine and Health Sciences, Ghent University – sequence: 18 givenname: Jeffrey L surname: Wrana fullname: Wrana, Jeffrey L email: wrana@lunenfeld.ca organization: Centre for Systems Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital – sequence: 19 givenname: Frederick P surname: Roth fullname: Roth, Frederick P email: fritz_roth@hms.harvard.edu organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School – sequence: 20 givenname: Marc surname: Vidal fullname: Vidal, Marc email: marc_vidal@dfci.harvard.edu organization: Center for Cancer Systems Biology (CCSB) and Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Genetics, Harvard Medical School |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19060903$$D View this record in MEDLINE/PubMed |
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Snippet | Use of the protein-protein interaction reference sets reported in this issue in Venkatesan
et al
. to benchmark four complementary protein-protein interaction... Information on protein-protein interactions is of central importance for many areas of biomedical research. At present no method exists to systematically and... Information on protein-protein interactions is of central importance for many areas of biomedical research. Currently no method exists to systematically and... |
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SubjectTerms | Analysis Animals Bioinformatics Biological Microscopy Biological Techniques Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedical research Evaluation Humans Life Sciences Mass spectrometry Protein Binding Protein Interaction Mapping - methods Protein microarrays Protein-protein interactions Proteins - analysis Proteins - metabolism Proteomics Quality control Research methodology Sensitivity and Specificity |
Title | An experimentally derived confidence score for binary protein-protein interactions |
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