Taipei Medical University

Translational Medicine 2: Target Discovery & Analysis

Taipei Medical University

Translational Medicine 2: Target Discovery & Analysis

Yi-Fan Chen

Instructor: Yi-Fan Chen

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Gain insight into a topic and learn the fundamentals.
Intermediate level

Recommended experience

7 hours to complete
Flexible schedule
Learn at your own pace
Gain insight into a topic and learn the fundamentals.
Intermediate level

Recommended experience

7 hours to complete
Flexible schedule
Learn at your own pace

What you'll learn

  • Analyze how researchers identify and validate promising drug targets in complex diseases like cancer

  • Evaluate how structural biology techniques guide the design of more effective, precise therapeutics

  • Design a biomarker strategy to track drug safety and effectiveness through clinical development

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Recently updated!

September 2026

Assessments

4 assignments

Taught in English

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There are 3 modules in this course

This module traces how the Yeast Two-Hybrid (Y2H) system evolved from a protein-interaction detection tool into a platform for cancer drug discovery. It includes content on proteomics fundamentals and interaction-detection methods, the Y2H principle and bait-prey design along with variant systems like reverse two-hybrid and split-ubiquitin screening, and the experimental workflow from plasmid construction to colony validation, closing with case studies on Smad4 SUMOylation, HSP27/Livin peptide aptamer screens, and Ras-Raf inhibitor discovery. By the end, you will be able to explain the Y2H reporter system's logic, design bait/prey plasmids and cDNA library screens, interpret interaction data, and connect Y2H results to cancer drug discovery pipelines.

What's included

8 videos2 readings1 assignment1 discussion prompt

This module introduces structural biology as an essential framework for understanding how biological macromolecules perform their functions. Because macromolecules, such as proteins, range from only one to ten nanometers in size, they exist far beyond the resolution limits of standard optical microscopes. Consequently, their structures cannot be observed directly. To overcome this fundamental limitation, scientists must rely on advanced physical techniques, primarily X-ray crystallography, to accurately visualize and map their precise three-dimensional atomic structures, which fundamentally dictate their biological mechanisms and interactions within the cell.

What's included

3 videos3 readings1 assignment1 discussion prompt

This module introduces translational medicine, tracing how discoveries move from basic laboratory research toward clinical application. It begins with an overview of cancer biology, then focuses on post-translational modification (PTM), a regulatory layer that lets a limited set of genes generate much greater protein functional diversity, shaping cell survival, inflammation, and tumor progression. The ubiquitination system is presented as the central case study: a quality-control mechanism that determines protein fate, whose dysregulation is linked to cancer. The module then draws on research examples from liver, breast, and pancreatic cancer, showing how specific regulatory proteins affect tumor survival and signaling, and their potential as future biomarkers.

What's included

8 videos2 readings2 assignments1 discussion prompt

Instructor

Yi-Fan Chen
Taipei Medical University
3 Courses176 learners

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