Guclu Tandac F, Tayhan Busra, Cetin Ebru, Atilgan Ali Rana, Atilgan Canan
Faculty of Natural Sciences and Engineering, Sabanci University, Tuzla, 34956, Istanbul, Turkey.
bioRxiv. 2024 Aug 20:2024.08.20.608765. doi: 10.1101/2024.08.20.608765.
Antibiotic resistance presents a significant challenge to public health, as bacteria can develop resistance to antibiotics through random mutations during their life cycles, making the drugs ineffective. Understanding how these mutations contribute to drug resistance at the molecular level is crucial for designing new treatment approaches. Recent advancements in molecular biology tools have made it possible to conduct comprehensive analyses of protein mutations. Computational methods for assessing molecular fitness, such as binding energies, are not as precise as experimental techniques like deep mutational scanning. Although full atomistic alchemical free energy calculations offer the necessary precision, they are seldom used to assess high throughput data as they require significantly more computational resources. We generated a computational library using deep mutational scanning for dihydrofolate reductase (DHFR), a protein commonly studied in antibiotic resistance research. Due to resource limitations, we analyzed 33 out of 159 positions, identifying 16 single amino acid replacements. Calculations were conducted for DHFR in its drug-free state and in the presence of two different inhibitors. We demonstrate the feasibility of such calculations, made possible due to the enhancements in computational resources and their optimized use.
抗生素耐药性对公共卫生构成了重大挑战,因为细菌在其生命周期中可通过随机突变产生对抗生素的耐药性,从而使药物失效。了解这些突变如何在分子水平上导致耐药性对于设计新的治疗方法至关重要。分子生物学工具的最新进展使得对蛋白质突变进行全面分析成为可能。评估分子适应性的计算方法,如结合能,不如深度突变扫描等实验技术精确。尽管全原子炼金术自由能计算提供了必要的精度,但由于需要大量更多的计算资源,它们很少用于评估高通量数据。我们使用深度突变扫描生成了二氢叶酸还原酶(DHFR)的计算文库,DHFR是抗生素耐药性研究中常用研究的一种蛋白质。由于资源限制,我们分析了159个位置中的33个,鉴定出16个单氨基酸替换。对处于无药物状态以及存在两种不同抑制剂情况下的DHFR进行了计算。我们证明了由于计算资源的增强及其优化使用,此类计算是可行的。