药物发现
生物分子
纳米技术
等温滴定量热法
材料科学
化学
计算生物学
生物
物理化学
生物化学
作者
Ashish Mehta,Rahul Makhija,Pallavi Barik,Shubham Dhiman,Ghanshyam Das Gupta,Vivek Asati
出处
期刊:Current Analytical Chemistry
[Bentham Science]
日期:2024-04-04
卷期号:20 (7): 449-470
标识
DOI:10.2174/0115734110296435240323113938
摘要
Abstract: Biophysical techniques include various methodologies applied in studying biological systems at the molecular and cellular level for the drug discovery process. Various methods like isothermal calorimetry, electron microscopy, XRD (X-ray diffraction), electron microscopy, mass spectrometry, atomic force microscopy, differential scanning calorimetry, surface plasmon resonance, and nuclear magnetic resonance are important techniques for drug discovery. Out of these techniques, XRD is widely employed in structure-based drug discovery, whereas FBDD (fragment-based drug discovery) is widely used in the different phases of drug discovery. XRD was considered one of the most important tools for structure determination of biomolecules and peptides. Consistent development and advancement in XRD improved the various aspects of data processing, collection, sample loading, and increased throughput. This advancement is crucial in obtaining highly resolved protein and other biomolecule crystal structures. The structure obtained from XRD forms the core of structure-based drug discovery and FBDD. This review article focuses on the different roles of biophysical techniques with special emphasis on advancement, data collection, and XRD's role in different drug discovery phases.
科研通智能强力驱动
Strongly Powered by AbleSci AI