MOLECULAR DOCKING AND RELATED DRUG DESIGN ACHIEVEMENTS

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MOLECULAR DOCKING AND RELATED DRUG DESIGN ACHIEVEMENTS

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MOLECULAR DOCKING AND RELATED DRUG DESIGN ACHIEVEMENTS

  1. 1. 1
  2. 2. Presented by: Guided by: Mr. Santosh Sahadeo Kumbhar M. Pharm.(Sem-I) Dr. M. S. Bhatia Head of Department DEPARTMENT OF PHARMACEUTICAL CHEMISTRY. BHARATI VIDYAPEETH COLLEGE OF PHARMACY, KOLHAPUR. 2
  3. 3. Contents Introduction. Definitions. Role of Bioinformatics. Introduction Types of Docking. Drug Discovery Process. Types of Docking Softwares. Applications of Docking. Achievements in Docking. Conclusion. References. 3
  4. 4. Abbreviations CADD - Computer Aided Drug Design. QSAR - Quantitative Structure Activity Relationship. SARs - Structure-Activity Relationships. HTS - High Through put Screening. 4
  5. 5. Introduction • Drug discovery  take years to decade for discovering a new drug and very costly • Effort  to cut down the research timeline and cost by reducing wet-lab experiment  use computer modelling. 5
  6. 6. Drug targets • • • • • Enzyme – inhibitors Receptors - agonists or antagonists Ion channel – blockers Transporter –inhibitors DNA - blockers 6
  7. 7. What is CADD????? Computational Chemistry/CADD is the chemistry whose major goals are to create efficient mathematical approximations and computer programs that calculate the properties of future drug molecules and thus helping in the process of drug design and discovery. 7
  8. 8. Why CADD…? Drug Discovery today are facing a serious challenge because of the increased cost and enormous amount of time taken to discover a new drug, and also because of rigorous competition amongst different pharmaceutical companies. 8
  9. 9. Molecular Docking 9
  10. 10. What is Docking? Docking attempts to find the “best” matching between two molecules. 10
  11. 11. … a more serious definition… Given two biological molecules determine: - Whether the two molecules “interact” - If so, what is the orientation that maximizes the “interaction” while minimizing the total “energy” of the complex. • Goal: To be able to search a database of molecular structures and retrieve all molecules that can interact with the query structure. 11
  12. 12. Some other definitions… Ligand or key – The complementary partner molecule which binds to the receptor. Ligands are most often small molecules also other biopolymer. Receptor or lock – The "receiving" molecule, most commonly a protein or other biopolymer. Docking – Computational simulation of a candidate ligand binding to a receptor. 12
  13. 13. Why is docking important? • It is the key to rational drug design. • The results of docking can be used to find inhibitors for specific target proteins and thus to design new drugs. • It is gaining importance as the number of proteins whose structure is known increases. 13
  14. 14. Why We Do Docking? • Drug discovery costs are too high: ~$800 millions, 8~14 years, ~10,000 compounds (DiMasi et al. 2003; Dickson & Gagnon 2004) • Drugs interact with their receptors in a highly specific and complementary manner. • Core of the target-based structure-based drug design (SBDD) for lead generation and optimization. Lead is a compound that – shows biological activity, – is novel, and – has the potential of being structurally modified for improved bioactivity, selectivity. 14
  15. 15. TRADITIONAL DRUG DESIGN Lead generation: Natural ligand / Screening Biological Testing Drug Design Cycle If promising Synthesis of New Compounds Pre-Clinical Studies 15
  16. 16. Modern Drug Discovery Process Natural ligand / Screening Molecular Biology & Protein Chemistry 3D Structure Determination of Target and Target-Ligand Complex Modelling Drug Design Cycle Structure Analysis and Compound Design Biological Testing If promising Synthesis of New Compounds Pre-Clinical Studies 16
  17. 17. Structure-based Drug Design (SBDD)   Drug targets (usually proteins) Binding of ligand to the target (docking) “rational” drug design (benefits = saved time and ₨₨₨) & 17
  18. 18. Structure-based Drug Design (SBDD) Ligand database Target Protein Molecular docking Ligand docked into protein’s active site Pharmacokinetic and Pharmacodynamic optimization 18
  19. 19. Applications of Bioinformatics Pharma Industry/ Molecular Medicine Biotechnology 19
  20. 20. Types of Docking There are 2 types of docking, 1.Rigid docking 2.Flexible docking Rigid Docking In the rigid docking molecules are rigid, in 3D space of one of the molecule which brings it to an optimal fit with the other molecules in terms of a scoring function. Flexible Docking In flexible docking molecules are flexible ,confirmations of the receptor and the ligand molecules , as they appear in complex. 20
  21. 21. Types of Docking studies Protein-Protein Docking Both molecules are rigid Interaction produces no change in conformation Similar to lock-and key model 21
  22. 22. Continued… Protein-Ligand Docking Ligand is flexible but the receptor protein is rigid. Interaction produces conformational changes in ligand. 22
  23. 23. Some “real” Docking Thermolysin protein with one of its known inhibitors 23
  24. 24. ‹#›
  25. 25. Available Docking Software… 1. DOCK (1982,2001) 2. FlexX (1996) 3. Hammerhead (1996) 4. Surflex (2003) 5. SLIDE (2002) 6. AutoDock (1990,1998) 7. ICM (1994) 8. MCDock (1999) 9. GOLD (1997) 10.GemDock (2004) 11.FRED (2002) 12.Glide (2004) 13.Yucca (2005) 14. vLife(Biopredicta) 25
  26. 26. Application of Molecular Docking in Modern Drug Discovery • Determine the lowest free energy structures for the receptor ligand complex. • Search database and rank hits for lead generation. • Calculate the differential binding of a ligand to two different macromolecular receptors. • Study the geometry of a particular complex. • Propose modification of a lead molecules to optimize potency or other properties. • de novo design for lead generation. • Library design. 26
  27. 27. Application of Molecular Docking in Modern Drug Discovery Case StudyIdentification of Inhibitors for Simultaneous Inhibition of AntiCoagulation and Anti-Infamatory Activities of Snake venom Phospholipase A2. (1994) 169000 compounds Pharmacophore Based-screening 300 compounds Molecular docking 32 promising compounds 27
  28. 28. Growing Evidence of Achievements….!! Molecular Docking has resulted in several breakthrough classes of new drug. Drug Target Company Dorzolamid Carbonic anhydrase (Hypercapnic Vantilatory failure) Merck Sharp and Dohme (Harlow, UK) Saquinavir HIV protease Roche (Welwyn, UK) Relenza Neuraminidase Biota (Melbourne, Australia 28
  29. 29. Growing Evidence of Achievements….!! 1. Discovery of Indinavir, the HIV protease inhibitor. (1992) 2. Identification of Haloperidol as a lead compound in a structurebased design for non-peptide inhibitor of HIV. 3. Carbonic Anhydrase (treatment of glaucoma) (2002) 4. Renin (treatment of hypertension) 5. Dyhrofolate reductase (antibacterial) (1992) 6. Neuraminidase (antiviral) 7. HIV-1 aspartic proteinase (anti-acquired immunodeficiency syndrome) 29
  30. 30. Growing Evidence of Achievements…. !! 8. Trypanosomal glyceraldehyde-3-phosphate dehydrogenase (anti-parasitic) 9. Thymidylate synthase and purine nucleoside phosphorylase (anticancer) 10. Elastase (treatment of emphysema) 11. Collagenase (Rheumatoid and Osteoarthritis) 12. Phispholipase A2 (anti inflammatory) (1994) 13. Glycogen phosphorylase (treatment of diabetes mellitus) 14. Thrombine (1996) 30
  31. 31. Conclusion… 1.Molecular docking give the promising contributions to identification and optimization of ligand in modern drug discovery. 2.The combination of the chemical information of natural products with docking-based virtual screening will play an important role in drug discovery in the post-genomic era as more and more new potential targets emerge from the functional genomic studies. 3.Docking-based virtual screening lead to much higher hit rate than traditional screening methods. (e.g., HTS) 31
  32. 32. Future Directions Pharmaceutical history indicated that natural products provided a large number of drugs to the market. But, even for the currently used drug targets, available natural products have not been tested completely. Computational medicinal methods, can contribute its unique role in achieving the task of examining the interaction of all existing natural products with all possible targets and establishing thier rational use. 32
  33. 33. References Graham L. Patrick, An Introduction to Medicinal Chemistry 4th edition, 2012 pag. No. 352-356 Dr. Abdul Wadood , Molecular docking and its application toward modern drug discovery Dept. of Biochemistry Abdul Wali Khan University. Dr. Kumud Sarin, Bioinformatics and its Application in Drug Designing. E.M. Krovat, T. Steindl and T. Langer, Recent Advances in Docking and Scoring,2005 Bentham Science Publishers Ltd. 33
  34. 34. Question plssssssssssssssssssss…….. 34

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