Computer-Assisted Drug Design
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Download Thursday, June 11, 2026 UPDATE:
This program is currently unavailable for enrollment.
It may have been updated or discontinued.
Check for newer version in our catalog.
This program is currently unavailable for enrollment.
It may have been updated or discontinued.
Check for newer version in our catalog.
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Free Trial CoursesOutline:INTRODUCTION 1. Course Description 2. Objectives 3. CADD Overview 4. Progress Check PROTEIN DESIGN 5. Objectives 6. Protein Design 7. Protein Engineering 8. Therapeutic Peptides 9. Progress Check ANTIBODY ENGINEERING 10. Objectives 11. Antibody Structure 12. Antibody Engineering 13. Antibody Therapeutics 14. Phage Display 15. Progress Check DRUG DESIGN 16. Objectives 17. Small Molecule Design 18. SARs 19. Affinity and Selectivity 20. Structure Based Design 21. Drug Pharmacophores 22. Progress Check DRUG OPTIMIZATION 23. Objectives 24. Library Design 25. Lead Optimization 26. Applications: HIV 27. Progress Check | Objectives:List the four major applications of computers to drug design Give examples of the use of computers to design or modify proteins, antibodies, drugs, or drug libraries Specify the three major applications of protein Define what site-directed mutagenesis is Describe what a peptidomimetic is Describe the structure of the antibody molecule Specify the four major types of therapeutic antibodies Define the region of an antibody that recognizes foreign antigens Give three examples of antibody therapeutics List the nine steps involved in creating antibodies via phage display List the four physical-chemical principles used in small molecule drug design Describe how structure-activity relationships have been enhanced by high-throughput screening Define affinity and selectivity of a drug to its target receptor Specify the four major interactions involved in structure-based drug design Understand the key features of a drug pharmacophore List some of the parameters involved in designing combinatorial drug libraries Define the two major parameters in drug optimization that can benefit from drug design Specify the amino acids at the active site of HIV protease and the point of cleavage Name two drugs that are non-symmetric HIV protease inhibitors | |
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