1st Edition
3D Cell-Based Biosensors in Drug Discovery Programs Microtissue Engineering for High Throughput Screening
Introduction
Biosensors and Bioassays
Conventional Biosensors
Conventional Biosensor Applications
Cell-Based Biosensors versus Cell-Based Assays (Bioassays)
3D Cultures
Concluding Remarks
Target-Driven Drug Discovery
Drug Discovery and Development
The Taxol (Paclitaxel) Discovery Case
The Gleevec (Imatinib Mesylate) Dicovery Case
Target-Driven Drug Discovery Paradigm
The New Discovery Paradigm Promise
Concluding Remarks
3D versus 2D Cultures
Comparative Genomics and Proteomics
Transcriptional Profi ling Studies
Comparative GO Annotation Analysis
Proteomics Studies
Concluding Remarks
Comparative Structure and Function
Complex Physiological Relevance
Cardiomyocyte Contractility
Liver Cell Bile Canaliculi In Vitro
Nerve Cell Voltage-Gated Calcium Signaling
Concluding Remarks
Emerging Design Principles
Chemical Microenvironmental Factors
Cell Adhesion Molecules
Short-Range Chemistry
Long-Range Chemistry
Concluding Remarks
Spatial and Temporal Microenvironmental Factors
Nano- and Microstructured Surfaces
Scaffolds
Nano and Scaffold-Combined Structures
Temporal Factor
Concluding Remarks
Material Physical Property and Force Microenvironmental Factors
Basics
Stiffness-Dependent Responses
Force-Dependent Responses
Concluding Remarks
Proteomics as a Promising Tool in the Search for 3D Biomarkers
Why Search for Three-Dimensionality Biomarkers?
Cellular Adhesions
Signaling Pathways
Overview of Proteomics Techniques
Study Design and Methods
Concluding Remarks
Readout Present and Near Future
Readout Present and Near Future
Fluorescence-Based Readouts
Bioluminescence-Based Readouts
Label-Free Biosensor Readouts
Concluding Remarks
Ready-to-Use Commercial 3D Plates
Introduction
Algimatrix™
Extracel™
Ultra-Web™
Market Opportunities
Concluding Remarks
Technology Deployment Challenges and Opportunities
Challenges to Adopting 3D Cultures in HTS Programs
Typical HTS Laboratory and Assay Configurations
Just-in-Time Reagents Provision Model
Limited Value-Addition from 3D Culture Physiological Relevance: Transepithelium Drug Transport and Induction of Drug Metabolizing Enzyme Cases
Paucity of Conclusive Support of 3D Culture Superiority
Cases for 3D Cultures in Drug Discovery
Three Cases
The β1-Integrin Monoclonal Antibody Case
The Matrix Metalloproteinase Inhibitors Case
Resistance to the Chemotherapeutic Agents Case
Concluding Remarks
Ideal Case Study Design
Rationale for The Case Study
Why Hepatotoxicity?
Hepatotoxicity and hESC-Derived Hepatocyte-Like Cells
Study Design and Methods
Analysis and Expected Results
Appendix A: Patents for 3D Scaffolds
Appendix B: Current Drug Targets
Appendix C: Popular Cell Lines in Drug Discovery
Appendix D: Stem Cells in Drug Discovery
Index
Biography
William S. Kisaalita, PhD is professor and former coordinator of graduate engineering programs at the University of Georgia, where he also directs the Cellular Bioengineering Laboratory. The main research focus of his laboratory is cell-surface interactions with applications in cell-based biosensing in drug discovery. He has published more than 80 peer reviewed and trade press papers and made more than 100 poster and podium presentations. He has received numerous instructional awards including membership in the University of Georgia Teaching Academy. He is a member of ACS, AAAS, ASEE, and SBS. Dr. Kisaalita serves on the editorial boards of The Open Biotechnology Journal and The Journal of Community Engagement and Scholarship.






