At CD ComputaBio, we specialize in advanced protein characterization techniques, including Electronic Circular Dichroism (ECD) Characterization, to provide detailed insights into protein structures. Our state-of-the-art computational modeling services are designed to meet the needs of researchers and industry professionals seeking accurate and high-resolution data on protein conformations.
Electronic Circular Dichroism (ECD) refers to the differential absorption of left and right circularly polarized light by chiral molecules. It is a spectroscopic technique that provides valuable information regarding the secondary and tertiary structure of proteins. ECD is particularly sensitive to changes in the electronic environment of chromophores and can detect subtle conformational changes that other techniques might miss. By leveraging computational modeling, our ECD Characterization Service offers a robust and precise method to analyze protein structures, aiding in a deeper understanding of their functional properties.
Figure 1. Protein ECD Characterisation.(Wang X, et al.2020)
CD ComputaBio offers a comprehensive Protein Raman Spectrum Characterisation Service to help researchers overcome these challenges and extract meaningful insights from their Raman data.
| Services | Description |
| Protein Structural Characterization | Using ECD spectroscopy coupled with computational modeling, we offer a comprehensive analysis of protein secondary and tertiary structures. This includes:
|
| Conformational Change Detection | Proteins often undergo conformational changes in response to environmental factors such as pH, temperature, and binding interactions. Our service accurately detects these changes, providing insights into protein dynamics and stability. |
| Protein-Ligand Interaction Analysis | We analyze the impact of ligand binding on protein structure using ECD data, helping to elucidate the binding mechanisms and interaction sites. |
| Customized Computational Modeling | Our team of experts customizes computational models to fit your specific research needs, offering simulations that predict ECD spectra based on protein structures provided or derived. |
Drug Discovery and Development
Structural Biology

We simulate the physical movements of atoms and molecules to predict protein behavior.

These calculations provide detailed electronic structure data crucial for accurate ECD spectra prediction.

Our algorithm incorporates machine learning techniques to improve prediction accuracy and adapt to new data efficiently.
Our algorithm incorporates machine learning techniques to improve prediction accuracy and adapt to new data efficiently.
To benefit from our Protein ECD Characterization Services, clients are required to provide:
Once the analysis is complete, clients receive a comprehensive report outlining the results of the Protein ECD Characterization, including:
We utilize the latest technology in computational modeling and ECD spectroscopy to provide accurate and reliable data.
We tailor our services to meet your specific requirements, ensuring that the delivered solutions align perfectly with your research goals.
From sample preparation to data interpretation, we support you at every step, ensuring a seamless and informative experience.
CD ComputaBio offers state-of-the-art Protein ECD Characterization Services that leverage computational modeling to provide valuable insights into protein structure and function. Our services are designed to meet the diverse needs of researchers and industries seeking advanced solutions for protein characterization. Contact us today to learn more about how our services can support your research goals and accelerate your scientific discoveries in the field of protein analysis.
Who can benefit from Protein ECD Characterisation Services?
Various stakeholders in the biotech and pharmaceutical industries can benefit from Protein ECD Characterisation Services, including:
Research Scientists: Who are studying protein functions and therapeutic potentials.
Pharmaceutical Companies: Engaged in drug development projects that require precise protein interactions.
Academic Institutions: Conducting fundamental research in molecular biology, biochemistry, and related fields.
Diagnostic Laboratories: Developing assays based on specific protein functions and interactions.
What information can I expect to receive from Protein ECD Characterisation?
Upon completion of the Protein ECD Characterisation, you can expect a comprehensive report including:
Structural Data: Detailed three-dimensional structures obtained through X-ray Crystallography or NMR.
Biophysical Properties: Information related to stability, folding dynamics, and solubility of the extracellular domain.
Functional Insights: Results from binding assays that highlight interaction affinities and kinetics with ligands or other proteins.
Characterization of Modifications: Any post-translational modifications (PTMs) that may affect function and stability.
Suggestions for Further Studies: If needed, recommendations for additional analyses or experiments to deepen understanding.
How does computational modelling contribute to this service?
Computational modelling plays a significant role in Protein ECD Characterisation Service. It helps simulate and predict the electrochemical behaviour of proteins based on their molecular structure and composition. By using quantum mechanical calculations and molecular dynamics simulations, models can estimate the electron transfer rates, redox potentials, and other electrochemical parameters. This aids in interpreting the experimental ECD data and proposing possible mechanisms for the observed electrochemical responses. For instance, if the experimental ECD results show an unexpected redox peak, computational modelling can help determine if it's due to a conformational change or an interaction with another molecule.
What kind of proteins can be characterised using this service?
A wide range of proteins can be studied using Protein ECD Characterisation Service, including enzymes, receptors, and transport proteins. Proteins with redox-active centres, such as metalloproteins or those containing flavin cofactors, are particularly suitable. However, even proteins that are not traditionally considered redox-active can sometimes exhibit electrochemical responses under certain conditions, providing new insights into their properties. Let's say you have a newly discovered protein suspected of having a role in electron transfer processes. ECD characterisation can help confirm or refute this hypothesis.
Reference