Abstract

Accurate systems biology modeling requires a complete catalog of protein complexes and their constituent proteins. We discuss a graph-theoretic/statistical algorithm for local dynamic modeling of protein complexes using data from affinity purification-mass spectrometry experiments. The algorithm readily accommodates multicomplex membership by individual proteins and dynamic complex composition, two biological realities not accounted for in existing topological descriptions of the overall protein network. A likelihood-based objective function guides the protein complex modeling algorithm. With an accurate complex membership catalog in place, systems biology can proceed with greater precision.

Submitted: October 29, 2004 · Accepted: November 23, 2004 · Published: January 3, 2005

Recommended Citation

Scholtens, Denise and Gentleman, Robert (2004) "Making Sense of High-Throughput Protein-Protein Interaction Data," Statistical Applications in Genetics and Molecular Biology: Vol. 3 : Iss. 1, Article 39.
Available at: http://www.bepress.com/sagmb/vol3/iss1/art39