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Presentation by: Kyle Borge, David Byon, & Jim Hall

Presentation by: Kyle Borge, David Byon, & Jim Hall . Herpesviral Protein Networks and Their Interaction with the Human Proteome. reconstruction of a Herpes Virus capsid. Presentation by: Kyle Borge, David Byon, & Jim Hall . Introduction to the Herpesvirus. Large double-stranded DNA genomes

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Presentation by: Kyle Borge, David Byon, & Jim Hall

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  1. Presentation by: Kyle Borge, David Byon, & Jim Hall Herpesviral Protein Networks and Their Interaction with the Human Proteome reconstruction of a Herpes Virus capsid Presentation by: Kyle Borge, David Byon, & Jim Hall

  2. Introduction to the Herpesvirus • Large double-stranded DNA genomes • Eight different strains • Causes diseases ranging from cold sores to shingles • Vaccine available for Varicella-Zoster Virus (VZV) • Little known about protein interactions

  3. Types of Herpesviruses Investigated • Kaposi’s Sarcoma-associated Herpesvirus (KSHV) • In the gamma (γ) herpes virus phylogenetic class • Causes cancerous tumors • Mostly associated with HIV patients • Sequenced in 1996 • Genome is roughly 165 kbs • 89 open reading frames (ORFs) • 113 ORFs used in experiment (included 15 cytoplasmic and 5 external domains derived from transmembrane proteins) • Varicella-Zoster Virus (VZV) , in the alpha (α) herpesvirus phylogenetic class • Causes chicken pox in children and shingles in adults • Sequenced in 1986 • Genome is roughly 125 kbs • 69 open reading frames (ORFs) • 96 ORFs used in experiment (Included 13 cytoplasmic and 10 external domains derived from transmembrane proteins)

  4. Methods of Investigating Protein Protein Interactions (PPI) • Many Methods • The Y2H technique is one of the top techniques for detecting protein-protein interactions • This article used Y2H to investigate protein-protein interactions

  5. Y2H Advantages • http://www.dnatube.com/video/993/Plasmid-Cloning • Relatively simple (automated) • Quick • Inexpensive • Only need the sequenced genome (or sequence of interest) • Scalable, its possible to screen for interactions among many proteins creating a more high-throughput screen (ex. viral genome) • Protein/polypeptides can be from various sources; eukaryotes, prokaryotes, viruses and even artificial sequences…allows the comparison of interactomes w/in and between different species…in this paper, eukaryote (human) interactome vs. viral interactome

  6. Y2H Limitations • http://www.dnatube.com/video/993/Plasmid-Cloning • The Y2H system cant analyze some classes of proteins • Transmembrane proteins, specifically their hydrophobic regions which may prevent the protein from reaching the nucleus • Transcriptional activators; may activate transcription w/out any interaction • False-negatives • Y2H screen fails to detect a protein-protein interactions • False-positives • Y2H screen produces a positive result (characterized by reporter gene activity) where no protein-protein interaction took place • Ex. bait proteins activate, transcribing the reporter gene, w/out the binding of the AD (bait proteins act as transcriptional activators)

  7. Yeast’s GAL4 transcriptional activator • GAL4 transcriptional activator which splits into two separate fragments; a binding domain (BD) and an activating domain (AD)

  8. Y2H Method • ORFs selected from published sequences • Amplified by nested PCR • Made primer sets of ends of ORFs • Y2H bait and prey vectors • Vectors transformed into Y187 and AH109 haploid yeast cells creating pools; a bait pool and a prey pool • Bait and prey mated in quadruplicates • Positive diploid yeasts are selected

  9. Open Reading Frames (ORFs) • Every ORFs of both KSHV & VZV were cloned & ligated into both a bait and prey GAL4 vector • Bait • protein of interest • the protein is fused to the yeast Gal4 DNA-binding domain (DBD) • Prey • a protein/ORF fused to the Gal4 transcriptional activation domain (AD) • interacting protein • Physical interaction between the bait and prey brings the DNA-BD and an AD of Gal4 together, thus re-creating a transcriptionally active Gal4 hybrid • Gal4 activity can be assayed by the expression of reporter genes and selectable markers

  10. (1-2) ORFs cloned into vectors via Nested PCR • KSHV • 113 full-length and partial ORFs • including 15 cytoplasmic and 5 external domains derived from transmembrane proteins • VZV • 96 full-length and partial ORFs • including 13 cytoplasmic and 10 external domains derived from transmembrane proteins

  11. Yeast-Two-Hybrid • Prey pool: (target) • Each individual ORF sequence is cloned into the ‘prey’ vector (down stream of the GAL4 AD gene) and is essentially fused to the GAL4 AD gene • Ampr for selection • Hemagglutinin • Bait pool: • Each individual ORF sequence is also cloned into the ‘bait’ vector (down stream of the GAL4 DBD gene) and is essentially fused to the GAL4 DBD gene • vector conveys Kanr for selection

  12. …in a diploid cell. Yeast-Two-Hybrid Background

  13. Viral Protein Interactions in KSHV • 12,000 Viral Protein Interactions tested • Identified 123 nonredundant interacting protein pairs • 118/123 were novel • 7/123 were previously reported • Screen captures 5/7 (71%) of previously reported interactions • 50% of Y2H interactions confirmed by coimmunoprecipitation (CoIP)

  14. Viral Protein Interactions in KSHV

  15. Previously Reported Protein Interactions of KSHV

  16. Coimmunoprecipitation

  17. Verification of Predicted Interactions in other Herpesvirus Species

  18. Correlation Between Viral Protein Interaction and Expression Profile • Correlation between AEC and clustering coefficient • Used to propose static or dynamic interaction for viral hubs • Average expression correlation [AEC]was calculated • For random pairs of ORFs: 0.804 • For interacting pairs of ORFs: 0.839

  19. Protein Interaction Networks

  20. Network Terminology • Node – represents a protein • Edge – represents interaction between two nodes • Average (node) degree – the average number of neighbors or connections that any given node has • Power coefficient (g) – derived from an approximate power law degree distribution plotted on a bilogarithmic scale and fitted by linear regression • P value - (significance under linear regression) as fitted by a power-law degree distribution (‘‘scale-free’’ property) • Characteristic path length – the distance between two nodes • Diameter (d) - describes the interconnectedness of a network; defined as the average length of the shortest paths between any two nodes in the network • Clustering coefficient – A value given to depict the number of fold enrichment over comparable random networks (‘‘small-world’’ property) • Small world property/network – Any network that has characteristics of a relatively short path and dense cluster (high cluster coefficient)

  21. Topology of KSHV and VZV Interaction Network KSHV protein interaction network VZV protein interaction network

  22. Comparison of Protein Interaction Networks

  23. Power Law Distribution Comparison • http://www.dnatube.com/video/993/Plasmid-Cloning

  24. Removal of Nodes in KSHV Network

  25. Protein Interaction KSHV & Sequence Conservation to EBV

  26. Correlation Between Functional and Phylogenetic Herpesviral Classes

  27. Viral protein interactions between functional classes • http://www.dnatube.com/video/993/Plasmid-Cloning

  28. Viral Protein Interactions Between Phylogenetic Classes

  29. View of the Human-Herpesviral Networks Varicella-Zoster Virus Kaposi Sarcoma-associated Herpesvirus

  30. Power Coefficient of KSHV-Human Network

  31. Interplay between KSHV and Human Network

  32. Viral Host Network / Random Network Comparison

  33. Conclusions • Virus and host interactomes possess distinct network topologies • Integration of viral and host protein network may lead to better understanding of viral pathogenicity • Future interactome data from other viruses may improve understanding of functions of viral proteins and their phylogeny • Understanding networks may help to develop future therapies

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