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Institution

Institute for Systems Biology

NonprofitSeattle, Washington, United States
About: Institute for Systems Biology is a nonprofit organization based out in Seattle, Washington, United States. It is known for research contribution in the topics: Population & Proteomics. The organization has 1277 authors who have published 2777 publications receiving 353165 citations.


Papers
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Journal ArticleDOI
TL;DR: This study used ICAT technology and tandem mass spectrometry-based proteomics to systematically study protein expression in chronic pancreatitis and validated that cathepsin D, integrin β1, and plasminogen were overexpressed in both pancreatic cancer and chronic pancitis.

147 citations

Journal ArticleDOI
TL;DR: This work used chemical labeling to isolate surface-exposed proteins on sporozoites and identified these proteins by mass spectrometry, providing the first direct evidence that the Plasmodium surface proteins CSP and TRAP are glycosylated in sporzoites, a finding that could impact the selection of vaccine antigens.
Abstract: Malaria parasite infection is initiated by the mosquito-transmitted sporozoite stage, a highly motile invasive cell that targets hepatocytes in the liver for infection. A promising approach to developing a malaria vaccine is the use of proteins located on the sporozoite surface as antigens to elicit humoral immune responses that prevent the establishment of infection. Very little of the P. falciparum genome has been considered as potential vaccine targets, and candidate vaccines have been almost exclusively based on single antigens, generating the need for novel target identification. The most advanced malaria vaccine to date, RTS,S, a subunit vaccine consisting of a portion of the major surface protein circumsporozoite protein (CSP), conferred limited protection in Phase III trials, falling short of community-established vaccine efficacy goals. In striking contrast to the limited protection seen in current vaccine trials, sterilizing immunity can be achieved by immunization with radiation-attenuated sporozoites, suggesting that more potent protection may be achievable with a multivalent protein vaccine. Here, we provide the most comprehensive analysis to date of proteins located on the surface of or secreted by Plasmodium falciparum salivary gland sporozoites. We used chemical labeling to isolate surface-exposed proteins on sporozoites and identified these proteins by mass spectrometry. We validated several of these targets and also provide evidence that components of the inner membrane complex are in fact surface-exposed and accessible to antibodies in live sporozoites. Finally, our mass spectrometry data provide the first direct evidence that the Plasmodium surface proteins CSP and TRAP are glycosylated in sporozoites, a finding that could impact the selection of vaccine antigens.

147 citations

Journal ArticleDOI
Cheng-Jian Xu1, Cilla Söderhäll2, Mariona Bustamante, Nour Baïz3, Olena Gruzieva2, Ulrike Gehring4, Dan Mason5, Leda Chatzi6, Leda Chatzi7, Leda Chatzi8, Mikel Basterrechea, Sabrina Llop9, Maties Torrent, Francesco Forastiere, Maria Pia Fantini10, Karin C. Lødrup Carlsen11, Karin C. Lødrup Carlsen12, Tari Haahtela13, Andréanne Morin14, Marjan Kerkhof1, Simon Kebede Merid2, Bianca van Rijkom1, Soesma A Jankipersadsing1, Marc Jan Bonder1, Stephane Ballereau15, Stephane Ballereau16, Cornelis J. Vermeulen1, Raul Aguirre-Gamboa1, Johan C. de Jongste17, Henriette A. Smit4, Ashok Kumar18, Ashok Kumar2, Ashok Kumar19, Göran Pershagen2, Stefano Guerra20, Judith Garcia-Aymerich21, Dario Greco22, Lovisa E. Reinius2, Rosemary R. C. McEachan5, Raf Azad5, Vegard Hovland12, Petter Mowinckel12, Harri Alenius13, Harri Alenius2, Nanna Fyhrquist13, Nanna Fyhrquist2, Nathanaël Lemonnier23, Nathanaël Lemonnier16, Johann Pellet16, Charles Auffray16, Pieter van der Vlies1, Cleo C. van Diemen1, Yang Li1, Cisca Wijmenga1, Mihai G. Netea24, Miriam F. Moffatt25, William O.C.M. Cookson25, Josep M. Antó, Jean Bousquet26, Jean Bousquet27, Tiina Laatikainen25, Tiina Laatikainen28, Catherine Laprise29, Kai-Håkon Carlsen12, Kai-Håkon Carlsen11, Davide Gori10, Daniela Porta, Carmen Iñiguez9, Jose Ramon Bilbao30, Manolis Kogevinas, John Wright5, Bert Brunekreef4, Juha Kere31, Juha Kere2, Martijn C. Nawijn1, Isabella Annesi-Maesano3, J Sunyer, Erik Melén32, Erik Melén2, Erik Melén17, Gerard H. Koppelman1 
TL;DR: In this paper, a large-scale epigenome-wide association study (EWAS) within the Mechanisms of the Development of ALLergy (MeDALL) project was conducted to assess methylation profiles associated with childhood asthma.

147 citations

Journal ArticleDOI
Josep M. Antó, Jean Bousquet1, Jean Bousquet2, Mübeccel Akdis3, Charles Auffray4, Thomas Keil5, Isabelle Momas6, Dirkje S. Postma7, Rudolf Valenta8, Magnus Wickman9, Anne Cambon-Thomsen10, Tari Haahtela11, Bart N. Lambrecht12, Karin C. Lødrup Carlsen13, Gerard H. Koppelman7, Jordi Sunyer, Torsten Zuberbier5, I. Annesi-Maesano14, Albert Arno, Carsten Bindslev-Jensen15, Giuseppe De Carlo, Francesco Forastiere, Joachim Heinrich, Marek L. Kowalski16, Dieter Maier17, Erik Melén9, Henriette A. Smit18, Marie Standl, John Wright19, Anna Asarnoj20, Marta Benet, Natalia Ballardini21, Natalia Ballardini9, Judith Garcia-Aymerich, Ulrike Gehring18, Stefano Guerra, Cynthia Hohmann5, Inger Kull9, Christian Lupinek8, Mariona Pinart, I. Skrindo13, Marit Westman20, Delphine Smagghe2, Cezmi A. Akdis3, Niklas Andersson9, Claus Bachert22, Stephane Ballereau4, Ferran Ballester23, Xavier Basagaña, Anna Bedbrook, Anna Bergström9, Andrea von Berg, Bert Brunekreef18, Emilie Burte2, Kai-Håkon Carlsen13, Leda Chatzi24, Jonathan M. Coquet12, Mirela Curin8, Pascal Demoly1, Esben Eller15, Maria Pia Fantini25, Leena von Hertzen11, Vergard Hovland13, Bénédicte Jacquemin, Jocelyne Just26, Theresa Keller5, Renata Kiss8, Manolis Kogevinas, Sibylle Koletzko27, Susanne Lau5, Irina Lehmann28, Nicolas Lemonnier, Mika J. Mäkelä11, Jordi Mestres29, Peter Mowinckel13, Rachel Nadif2, Martijn C. Nawijn7, Johan Pellet4, Isabelle Pin, Daniela Porta, Fanny Rancière6, Emmanuelle Rial-Sebbag10, Yvan Saeys12, Martijn J. Schuijs12, Valérie Siroux2, Christina Tischer, Mathies Torrent, Raphaëlle Varraso2, Kalus Wenzel17, Cheng-Jian Xu7 
TL;DR: The translational component of MeDALL is shown by the identification of a novel allergic phenotype characterized by polysensitization and multimorbidity, which is associated with the frequency, persistence, and severity of allergic symptoms.
Abstract: Asthma, rhinitis, and eczema are complex diseases with multiple genetic and environmental factors interlinked through IgE-associated and non-IgE-associated mechanisms. Mechanisms of the Development of ALLergy (MeDALL; EU FP7-CP-IP; project no: 261357; 2010-2015) studied the complex links of allergic diseases at the clinical and mechanistic levels by linking epidemiologic, clinical, and mechanistic research, including in vivo and in vitro models. MeDALL integrated 14 European birth cohorts, including 44,010 participants and 160 cohort follow-ups between pregnancy and age 20 years. Thirteen thousand children were prospectively followed after puberty by using a newly standardized MeDALL Core Questionnaire. A microarray developed for allergen molecules with increased IgE sensitivity was obtained for 3,292 children. Estimates of air pollution exposure from previous studies were available for 10,000 children. Omics data included those from historical genome-wide association studies (23,000 children) and DNA methylation (2,173), targeted multiplex biomarker (1,427), and transcriptomic (723) studies. Using classical epidemiology and machine-learning methods in 16,147 children aged 4 years and 11,080 children aged 8 years, MeDALL showed the multimorbidity of eczema, rhinitis, and asthma and estimated that only 38% of multimorbidity was attributable to IgE sensitization. MeDALL has proposed a new vision of multimorbidity independent of IgE sensitization, and has shown that monosensitization and polysensitization represent 2 distinct phenotypes. The translational component of MeDALL is shown by the identification of a novel allergic phenotype characterized by polysensitization and multimorbidity, which is associated with the frequency, persistence, and severity of allergic symptoms. The results of MeDALL will help integrate personalized, predictive, preventative, and participatory approaches in allergic diseases.

146 citations


Authors

Showing all 1292 results

NameH-indexPapersCitations
Younan Xia216943175757
Ruedi Aebersold182879141881
David Haussler172488224960
Steven P. Gygi172704129173
Nahum Sonenberg167647104053
Leroy Hood158853128452
Mark H. Ellisman11763755289
Wei Zhang112118993641
John Ralph10944239238
Eric H. Davidson10645447058
James R. Heath10342558548
Alan Aderem9924646682
Anne-Claude Gingras9733640714
Trey Ideker9730672276
Michael H. Gelb9450634714
Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20233
202260
2021216
2020204
2019188
2018168