More Related Content
Similar to Introduction to bioinformatics.pptx
Similar to Introduction to bioinformatics.pptx (20)
Recently uploaded
Recently uploaded (20)
Introduction to bioinformatics.pptx
- 1. Introduction to bioinformatics Morteza Ghandadi PhD. of Pharmaceutical Biotechnology Mazandaran university of medical sciences 1
- 2. 2
- 3. Bioinformatics is an interdisciplinary field that develops methods and software tools for understanding biological data 3
- 4. History • The first protein was sequenced (1955) • Margaret O.Dayhoff • Atlas of Protein Sequence and Structure (1965) • Paulien Hogeweg and Ben Hesper coined “bioinformatics” in 1970 • The protein data bank (1973) • DNA sequencing (1977) • NCBI( 1988) • Human genome project lunched (1990) • The human genome is published (2001) https://www.smithsonianmag.com/science- nature/how-margaret-dayhoff-helped-bring- computing-scientific-research-180971904/ 4
- 7. Unites Of Information In Biological Macromolecules DNA Sequence analysis Mutation and polymorphism studies Identification of regulatory regions Gene finding Genome annotation Comparative genomics RNA RNA sequencing Splice variants Tissue expression level MicroArray Single gene analysis Sequence contigs Protein Homology modeling Structure function prediction Ligand docking Protein-protein interaction Protein expression Phylogenic analysis 7
- 9. Develop templates to develop potent drug molecules • Structural analysis of secretory phospholipase A2 from Clonorchis sinensis https://link.springer.com/article/10.1007/s00894-011-1333-8 9
- 13. Protein interaction studies and pathway analysis https://pubmed.ncbi.nlm.nih.gov/26997873/ 13
- 14. Deciphering the molecular basis of disease https://pubmed.ncbi.nlm.nih.gov/27585677/ 14
- 15. Pharmacophore modeling and docking 15
- 16. Pharmacophore modeling and docking 16
- 17. Pathogenesis of drug toxicity https://link.springer.com/article/10.1007/s00894-011-1289-8 17
- 18. Vaccine designing and development 18
- 19. Tumor antigens • The ideal antigen for a cancer vaccine should be highly immunogenic, explicitly expressed in all cancer cells (not in normal cells) and necessary for the survival of cancer cells • Tumor-associated antigens (TAAs) • Tumor-specific antigens (TSAs)
- 22. Bioinformatics journals • Briefings in Bioinformatics • Bioinformatics • Genomics, Proteomics & Bioinformatics • Current Bioinformatics • BMC Bioinformatics • Computers in Biology and Medicine • Journal of Computer-Aided Molecular Design • In Silico Biology • Journal of molecular modeling 22
- 24. Databases 24
- 26. Gene • A searchable database of genes, focusing on genomes that have been completely sequenced and that have an active research community to contribute gene-specific data. Information includes nomenclature, chromosomal localization, gene products and their attributes (e.g., protein interactions), associated markers, phenotypes, interactions, and links to citations, sequences, variation details, maps, expression reports, homologs, protein domain content, and external databases 26
- 27. 27
- 28. Genome • Contains sequence and map data from the whole genomes of over 1000 organisms. The genomes represent both completely sequenced organisms and those for which sequencing is in progress. All three main domains of life (bacteria, archaea, and eukaryota) are represented, as well as many viruses, phages, viroids, plasmids, and organelles. 28
- 29. 29
- 30. Nucleotide • A collection of nucleotide sequences from several sources, including GenBank, RefSeq, the Third Party Annotation (TPA) database, and PDB. Searching the Nucleotide Database will yield available results from each of its component databases. 30
- 31. 31
- 32. RefSeq: NCBI Reference Sequence Database • A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein. 32
- 33. What is the difference between RefSeq and GenBank? • GenBank sequence records are owned by the original submitter and cannot be altered by a third party. RefSeq sequences are not part of the INSDC but are derived from INSDC sequences to provide non- redundant curated data representing our current knowledge of known genes 33
- 34. BLAST • The Basic Local Alignment Search Tool (BLAST) finds regions of local similarity between sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. BLAST can be used to infer functional and evolutionary relationships between sequences as well as help identify members of gene families. 34
- 35. 35
- 36. Protein • The Protein database is a collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB. Protein sequences are the fundamental determinants of biological structure and function. 36
- 37. UniProt • Universal Protein Resource (UniProt) is a comprehensive resource for protein sequence and annotation data. The UniProt databases are the UniProt Knowledgebase (UniProtKB), the UniProt Reference Clusters (UniRef), and the UniProt Archive (UniParc). UniProt is a collaboration between the European Bioinformatics Institute (EMBL-EBI), the SIB Swiss Institute of Bioinformatics and the Protein Information Resource (PIR). 37
- 38. 38
- 39. 39
- 40. 40
- 41. Protein Data Bank (PDB) • The Protein Data Bank (PDB) is a database for the three-dimensional structural data of large biological molecules, such as proteins and nucleic acids. 41
- 42. 42
- 43. 43
- 44. 44
- 45. 45
Editor's Notes
- The active site of the enzyme shows the classical features of PLA2 with the participation of the three residues: histidine-aspartic acid-tyrosine in hydrogen bond formation. This is an interesting variation from the house keeping group III PLA2 enzyme of human which has a histidine-aspartic acid and phenylalanine arrangement at the active site. This difference is therefore an important structural parameter that can be exploited to design specific inhibitor molecules against the pathogen PLA2
- In this study, a detailed structural and ligand binding analysis of the isoforms has been done by modeling. The overall three dimensional structures of the isoforms are well conserved with three helices and a bwing stabilized by four disulfide bonds. There are characteristic differences at the calcium binding loop, hydrophobic channel and the C-terminal domain that can potentially be exploited for drug binding. But the most significant feature pertains to the catalytic site where the isoforms exhibit three variations of either a histidineaspartate- tyrosine or histidine-glutamate-tyrosine or histidine- aspartate-phenylalanine. Molecular docking studies show that isoform specific residues and their conformations in the substrate binding hydrophobic channel make unique interactions with certain inhibitor molecules resulting in a perfect tight fit.
- Fluorescence-based differential in-gel expression coupled with mass spectrometric analysis was used for discovery phase of experiments, and real-time polymerase chain reaction, Western blotting, and pathway analysis were performed for expression and functional validation of differentially expressed proteins. While aldehyde reductase, hnRNP, cyclophilin A, heat shock protein-27, and actin are upregulated in responders, prohibitin, enoyl-coA hydratase, peroxiredoxin, and fibrin- are upregulated in the nonresponders. The expressions of some of these proteins correlated with increased apoptotic activity in responders and decreased apoptotic activity in nonresponders. Therefore, the proteins qualify as potential biomarkers to predict chemotherapy response.
- These differences include: (1) loop-L3 between H2 and H3, which bears residue Gly80 in the wild type, is in a closed conformation with respect to the channel opening, while in the mutant enzyme it adopts a relatively open conformation; (2) the mutant enzyme is less compact and has higher solvent accessible surface area; and (3) interfacial binding contact surface area is greater, and the quality of interactions with the receptor is better in the mutant enzyme as compared to the wild type. Therefore, the structural differences delineated in this study are potential biophysical factors that could determine the increased potency of the mutant enzyme with macrophage receptor for cytokine secreting function, resulting in exacerbation of cachexia in COPD.
- The gentamicin molecule binds to the lectin site of the calreticulin and lies in the concave channel formed by the long beta sheets. It makes interactions with residues Tyr109, Asp125, Asp135, Asp317 and Trp319 which are crucial for the chaperone function of the calreticulin. The superimposing of the modeled complex with the only available crystal structure complex of calreticulin with a tetrasaccharide (Glc1Man3) shows interesting features. First, the rings of the gentamicin occupy the positions of glucose and the first two mannose sugars of the tetrasaccharide molecule. Second, the oxygen atoms of the glycosidic linkage of these two ligands have a positional deviation of 1.3 Ǻ
- TAAs include “self-antigens” such as differentiated antigens, overexpressed antigens, cancer-testicular antigens, and viral-original “non-self” antigens
- International Nucleotide Sequence Database Collaboration (INSDC)