Antibody-ligand interactions: computational modeling and correlation with biophysical measurements
| Autor: | J M Anchin, S Y Tetin, Thomas R. Ioerger, D S Linthicum |
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| Rok vydání: | 2001 |
| Předmět: |
Models
Molecular Circular dichroism Molecular model Chemistry Protein Conformation Organic Chemistry Static Electricity Solvation General Medicine Ligands Fluorescence spectroscopy Antibodies Computer Science Applications Hydrophobic effect Partial charge Protein structure Chemical physics Drug Discovery Static electricity Biophysics Computer Simulation |
| Zdroj: | Combinatorial chemistryhigh throughput screening. 4(5) |
| ISSN: | 1386-2073 |
| Popis: | Several new aspects of computer-assisted molecular modeling strategies and biophysical techniques, such as fluorescence spectroscopy, circular dichroism, and absorption spectroscopy, have proved useful in the analysis and description of antibody-ligand interactions. The molecular features involved in determining the specificity of antibody-ligand interactions, such as electrostatics (e.g. partial charges, salt bridges, p-cation motifs), hydrogen-bonds, polarization, hydrophobic interactions, hydration and solvation effects, entropy, and kinetics can be identified using a battery of biophysical techniques. An understanding of these parameters is essential to our use of antibodies as tools in high throughput screening of chemical libraries for the discovery of novel compounds. |
| Databáze: | OpenAIRE |
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