Related Experiment Video
Updated: Jul 12, 2026

Structure-Guided Design and Development of Novel Cyclophilin A Inhibitors and Ganoderiol-F Derivatives: An In-Silico Approach
Published on: June 23, 2026
Protein-ligand interactions by QCM: challenges and resolutions
Olga Volkova1, Anastasia Serova1, Ekaterina Skorb1
1Infochemistry Scientific Center, ITMO University, 191002 Saint Petersburg, Russia.
Quartz crystal microbalance (QCM) offers sensitive, label-free detection of biomolecular interactions for drug discovery. This review details strategies to enhance QCM
Area of Science:
- Biochemistry
- Analytical Chemistry
- Biosensor Technology
Background:
- Label-free, real-time analysis of biomolecular interactions is crucial for drug discovery.
- Existing techniques like Surface Plasmon Resonance (SPR) and Isothermal Titration Calorimetry (ITC) have limitations.
- Quartz Crystal Microbalance (QCM) presents a highly sensitive alternative for mass-based detection.
Purpose of the Study:
- To highlight Quartz Crystal Microbalance (QCM) as a key technology for label-free, real-time biomolecular interaction analysis.
- To focus on the application of QCM in protein-ligand binding studies within drug discovery.
- To provide a comprehensive framework of theoretical principles and practical solutions for QCM implementation.
Main Methods:
- Review of QCM principles and its application in analyzing biomolecular binding kinetics.
- Discussion of strategies for optimizing protein immobilization on QCM sensors.
- Analysis of methods for interpreting low-mass ligand binding signals.
- Comparison of QCM sensitivity and performance against SPR and ITC.
Main Results:
- QCM demonstrates exceptional sensitivity to nanogram-level mass changes, enabling detection of low-affinity interactions.
- Effective strategies for protein immobilization and signal interpretation in QCM assays were consolidated.
- QCM offers a viable label-free, real-time alternative to established methods like SPR and ITC for specific applications.
Conclusions:
- QCM is a powerful and sensitive tool for label-free, real-time analysis of biomolecular interactions, particularly protein-ligand binding.
- Addressing challenges in immobilization and signal interpretation can significantly advance QCM utility in drug discovery.
- The review provides a foundation for expanding QCM applications in rational drug design, diagnostics, and environmental monitoring.
Related Concept Videos
Ligand Binding Sites
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
Ligand Binding Sites
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
The Equilibrium Binding Constant and Binding Strength
The Equilibrium Binding Constant and Binding Strength
Ligand Binding and Linkage
Ligand Binding and Linkage
