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Illinois Bio-Grid Grid Computing The Illinois Bio-Grid Alexander B. Schilling, Ph.D. University of Chicago Proteomics Core Lab [email protected] Outline Illinois Bio-Grid • Bio-Medical Informatics – Show how computability is growing exponentially • Illinois Bio-Grid – Describe this Grid founded at DePaul • IBG Workbench – Describe these grid enabled BioInformatics tools • Mass Spec Toolkit in Cactus – Describe plans to implement tools for spectral interpretation in Cactus BioInformatics and Computability Illinois Bio-Grid • Growth of data in GenBank is exponential and doesn't show signs of slowing down yet. – Source GenBank/NCBI • Compute time to process data growing equivalently – Twice Moore's law • Biologists don't have access to supercomputers for everyday work • Grid computing gives Biologists more computing power affordably Illinois Bio-Grid Illinois Bio-Grid • A consortium of – – – – – Educational Institutions National Labs Private Industry City & State entities Museums Goals Illinois Bio-Grid 1. Provide an infrastructure of computational (and other) resources to Biological and Medical researchers 2. Provide an infrastructure of computational (and other) resources to Computer Scientists working on BioMedical problems 3. Provide a tool suite of BioMedical software for BioMedical researchers to use on the IBG computational resources – Also for open source distribution worldwide 4. Provide an environment for CS researchers to work with BioMedical researchers 5. Try to solve some computationally intense BioMedical Informatics problems 6. Create a workbench of BioMedical software modules in open source distribution to facilitate more rapid BioMedical Informatics research by researchers worldwide Illinois Bio-Grid Illinois Bio-Grid Infrastructure DePaul Chicago Technology Park (Supercomputing Center Of Chicago) Argonne MCS U Chicago Canadian NRC Field Museum IIT Bio-Grid Workbench Illinois Bio-Grid • Consists of many applications important to Biological and Medical Researchers • All Grid enabled to provide enhanced computational power • Genomics • Proteomics • Phylogenetics • Computational Fluid Dynamics / Medical Imaging • Cell membrane modeling • Data Modeling LSG-RG in GGF Reference Implementation Genomics and Proteomics 1 Illinois Bio-Grid • Homology Searching – Searching for proteins with the same evolutionary "ancestor" – Smith-Waterman / Blast / FastA – Database against database searches (instead of single sequence against database searches) – Allow groups of input sequences to search for homologous sequences to all in the set • Mass Spec Data Interpretation – Ionize peptides and fragment them inside mass spectrometer – Measure charge/mass ratio of peptide ions and fragments – Interpret resulting spectra Intens. Al l , 0.0-0.5mi n (#1-#10) 1250 1000 1479.9 1640.0 1305.9 750 1420.8 1249.9 500 441.1 1882.9 1163.9 1780.8 250 562.1 0 400 600 800 1000 1200 1400 1600 1800 2000 m/z Genomics and Proteomics 2 Illinois Bio-Grid • Mass Spec Based Protein Identification – Conduct “In Silico” Digestion of protein database – Predict charge/mass ratio of all possible peptide ions resulting from database – Search actual ions in spectra against predicted ions – Return identifications of proteins based on scoring match Genomics and Proteomics 3 Illinois Bio-Grid • • • • Predict 3D Protein folding given sequence of amino acids Solution to Schrödinger equation is intractable Search space of possible folds is immense Current methods of searching – – – – – ab-initio AI Lego Monte Carlo Lattice • On Grids can run multiple searches – In parallel – In series • On Grids can run at higher resolutions Phylogenetics Illinois Bio-Grid • Sequence various taxa (individuals or species) – Frequently sequence mitochondrial DNA – Mitochondrial DNA much like prokaryote DNA • Compare sequences – Form hypothetical evolutionary tree – Each branch is a mutation – Shows mutations from hypothetical ancestor • Search space is immense – Runs for 6 months on a single processor – Then crashes! Computational Fluid Dynamics / Medical Imaging Illinois Bio-Grid • Monitor and collect real time CAT scan data – Arterial blood flow • Use Grid to interpret data – – – – Use Computational Fluid Dynamics to model blood flow Produce real time imaging Locate aneurisms and other anomalies Aid in diagnosis and decision making for surgical procedures – Non-invasive Cell membrane modeling Illinois Bio-Grid • Run simulations using both – Configurational Bias Monte Carlo Method (CBMC) – Molecular Dynamics (MD) • Current simulations being done involve the properties of cholesterol in lipid membranes – Cholesterol is known to be an essential component of mammalian cell membranes – Its exact role is not well understood • Previous simulations have been run – Up to 1600 lipid or cholesterol molecules – And 52,000 water molecules • We're increasing these simulations by – An order of magnitude in the physical dimensions – And 2 to 3 orders of magnitude in time Data Modeling Illinois Bio-Grid • Data Modeling LSG-RG in GGF Reference Implementation – Automatic Data Synchronization – Flagging "dirty" data – Flagging data sources (including versioning) IBG Workbench Illinois Bio-Grid Phylogenetic Trees Mass Spec Proteomics Homology Searching DB Access Grid Services (Middleware) Grid Fabric (Resources) Membrane Modeling CFD Illinois Bio-Grid The Purpose of Mass Spectrometry in Proteomics • Identify and sequence all proteins involved in an organism’s biology. • Use this knowledge to identify proteins (or peptides) that can be used to study and understand different biological states. • Correlate protein expression levels to biological function. Use protein or peptide biomarkers to identify disease states in patients. • Use the structure of the relevant proteins as targets for developing new therapeutic techniques (drugs etc..). Illinois Bio-Grid Mass Spectrometers in Proteomics • • • • • • Mass spectrometers measure the masses of proteins and peptides by moving their ions through the instrument in a controlled way. Proteins can be degraded using enzymes and the peptides produced can be analyzed by the mass spectrometer. A MS/MS instrument can cause the peptide ions to fragment into smaller pieces which can be used to deduce the peptide’s sequence. Once the sequence of the peptides has been determined, the protein’s complete sequence can be reassembled from the peptide sequences. The intensity of peaks can be used to determine the expression level of a protein in a sample. Samples from healthy and diseased tissue can be compared to locate biomarkers for disease. Illinois Bio-Grid • • • The MS/MS Experiment Produces Multidimensional Data Chromatograms (Time vs Intensity) Precursor Ion Spectra of Peptides (Mass vs Intensity) Product Ion Spectra of Peptides(*(Precursor Mass), Mass vs Intensity) +MS, +MS2(1535.8), 4.7min 5.6min (#44) 38. (#36) Intens. 1000 500 MS TIC 000 400 000 300 000 200 000 100 000 1+ 1479.8 MS 800 1+ 1640.0 1+ 646.4 600 1+ 1305.8 400 200 0 150 417.1 1+ 1578.7 1+ 1163.6 562.2 1+ 927.7 476.1 725.2 1710.0 1074.6 2076.8 845.1 2169.4 38. MS/MS of m/z 125 y7 100 1535.8 b6 1153.1 y11 1+ 1516.6 842.5 75 y5 50 659.9 599.3 25 0 400 1389.3 y6 600 1304.2 964.4 727.2 800 1000 1200 1400 1600 1800 2000 m/z Illinois Bio-Grid What the tandem mass spectrum of a peptide looks like. Y-ions from C to N terminus Y3 ion Y1 ion Y2 ion R2 O R3 O R4 O R1 O C N NH 2 C H H B1 ion C C H B2 ion N H C C N C C OH H H H B3 ion B-ions from N to C terminus Illinois Bio-Grid Important Issues In Computation for Proteomics • DeNovo Sequencing – – – – – • Many computationally efficient algorithms exist Many times algorithms produce incorrect results very quickly! Issue of posttranslational modifications introduces complexity into interpretations Much data must be discarded to accommodate workstation based computational capacity A strong desire exists to use intensity data as well as mass data in interpretations Database Search (Protein ID) – Most packages are commercial, few open source (BLAST based only) – The more posttranslational modifications you allow for, the longer the searches take. Area is ripe for parallelism. – Serious problems with false positive identifications • Many active in research to address this problem • Could be reduced by more front end interpretation before search • Could combine spectra from multiple MS types before search instead of correlating ID results after searches • Datamining – What do you do with all the identifications? Systems Biology! • Create models for signal pathways using protein id and expression data Illinois Bio-Grid GridProt: A Cactus Based Proteomics Tool Kit Thorns: GridMass – handles basic data extraction, chromatographic peak integration, mass detection GridTAG - partial sequence mass tag extraction GridID - grid based database search using mass spec data GridDeNS - grid based denovo sequencing Visualization – OpenDX Data Storage – mzXML and HDF-5 Conclusions Illinois Bio-Grid • Illinois Bio-Grid – Excellent resource for Biological and Medical researchers • IBG Workbench – Excellent software architecture for compute intensive applications – Will be source of BioMedical Informatics software sharing for a plethora of different research areas – Will be source of workbench tools for researchers in other related Informatics software creation • Cactus is an ideal platform for HPC of Mass Spec data – Modular thorns allow generalization for MS, specialization for Proteomics – Ideal base for open source, extendable software ready for HPC as Proteomics data sets grow. • http://facweb.cs.depaul.edu/bioinformatics • http://facweb1.cs.depaul.edu/~dangulo Illinois Bio-Grid Acknowledgements University of Chicago Howard Hughes Medical Institute Ben May Cancer Center Pfizer Inc. Illinois Biogrid: Dave Angulo, DePaul University Gregor von Laszewski, ANL Kevin Drew, Tim Freeman