| Literature DB >> 32950259 |
Lan Zhu1, Xiaoyu Chen1, Enrique E Abola1, Liang Jing1, Wei Liu2.
Abstract
Rational drug discovery has greatly accelerated the development of safer and more efficacious therapeutics, assisted significantly by insights from experimentally determined 3D structures of ligands in complex with their targets. Serial crystallography (SX) with X-ray free-electron lasers has enabled structural determination using micrometer- or nanometer-size crystals. This technology, applied in the past decade to solve structures of notoriously difficult-to-study drug targets at room temperature, has now been adapted for use in synchrotron radiation facilities. Ultrashort time scales allow time-resolved characterization of dynamic structural changes and pave the road to study the molecular mechanisms by 'molecular movie.' This article summarizes the latest progress in SX technology and deliberates its demanding applications in future structure-based drug discovery.Keywords: GPCR ligand swapping; X-ray free-electron laser (XFEL); serial femtosecond crystallography; structure-based drug discovery (SBDD); synchrotron-based serial crystallography; time-resolved serial crystallography
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Year: 2020 PMID: 32950259 PMCID: PMC7572805 DOI: 10.1016/j.tips.2020.08.009
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819