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Integration of cardiac proteome biology and medicine by a specialized knowledgebase

  • Nobel C. Zong
  • , Haomin Li
  • , Hua Li
  • , Maggie P.Y. Lam
  • , Rafael C. Jimenez
  • , Christina S. Kim
  • , Ning Deng
  • , Allen K. Kim
  • , Jeong Ho Choi
  • , Ivette Zelaya
  • , David Liem
  • , David Meyer
  • , Jacob Odeberg
  • , Caiyun Fang
  • , Hao Jie Lu
  • , Tao Xu
  • , James Weiss
  • , Huilong Duan
  • , Mathias Uhlen
  • , John R. Yates
  • Rolf Apweiler, Junbo Ge, Henning Hermjakob, Peipei Ping

Research output: Contribution to journalArticlepeer-review

Abstract

Rationale: Omics sciences enable a systems-level perspective in characterizing cardiovascular biology. Integration of diverse proteomics data via a computational strategy will catalyze the assembly of contextualized knowledge, foster discoveries through multidisciplinary investigations, and minimize unnecessary redundancy in research efforts. Objective: The goal of this project is to develop a consolidated cardiac proteome knowledgebase with novel bioinformatics pipeline and Web portals, thereby serving as a new resource to advance cardiovascular biology and medicine. Methods and results: We created Cardiac Organellar Protein Atlas Knowledgebase (COPaKB; www.HeartProteome.org), a centralized platform of high-quality cardiac proteomic data, bioinformatics tools, and relevant cardiovascular phenotypes. Currently, COPaKB features 8 organellar modules, comprising 4203 LC-MS/MS experiments from human, mouse, drosophila, and Caenorhabditis elegans, as well as expression images of 10 924 proteins in human myocardium. In addition, the Java-coded bioinformatics tools provided by COPaKB enable cardiovascular investigators in all disciplines to retrieve and analyze pertinent organellar protein properties of interest. Conclusions: COPaKB provides an innovative and interactive resource that connects research interests with the new biological discoveries in protein sciences. With an array of intuitive tools in this unified Web server, nonproteomics investigators can conveniently collaborate with proteomics specialists to dissect the molecular signatures of cardiovascular phenotypes.

Original languageEnglish (US)
Pages (from-to)1043-1053
Number of pages11
JournalCirculation research
Volume113
Issue number9
DOIs
StatePublished - Oct 12 2013
Externally publishedYes

Keywords

  • Computational biology
  • COPaKB
  • Mitochondria
  • Omics science
  • Organelles
  • Proteomics
  • Translational medical research

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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