Integrated machine learning-based virtual screening and biological evaluation for identification of potential inhibitors against cathepsin K

被引:1
作者
Parwez, Shahid [1 ,2 ]
Chaurasia, Animesh [1 ,2 ]
Mahapatra, Pinaki Parsad [1 ,2 ]
Ahmed, Shakil [1 ,2 ]
Siddiqi, Mohammad Imran [1 ,2 ]
机构
[1] Cent Drug Res Inst, Biochem & Struct Biol, CSIR, Sect 10,Jankipuram Extens,Sitapur Rd, Lucknow 226031, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
关键词
Cathepsin K; Deep Learning; Machine Learning; MM/PBSA; Osteoporosis; Virtual Screening; DOCKING;
D O I
10.1007/s11030-024-10845-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cathepsin K is a type of cysteine proteinase that is primarily expressed in osteoclasts and has a key role in the breakdown of bone matrix protein during bone resorption. Many studies suggest that the deficiency of cathepsin K is concomitant with a suppression of osteoclast functioning, therefore rendering the resorptive properties of cathepsin K the most prominent target for osteoporosis. This innovative work has identified a novel anti-osteoporotic agent against Cathepsin K by using a comparison of machine learning and deep learning-based virtual screening followed by their biological evaluation. Out of ten shortlisted compounds, five of the compounds (JFD02945, JFD02944, RJC01981, KM08968 and SB01934) exhibit more than 50% inhibition of the Cathepsin K activity at 0.1 mu M concentration and are considered to have a promising inhibitory effect against Cathepsin K. The comprehensive docking, MD simulation, and MM/PBSA investigations affirm the stable and effective interaction of these compounds with Cathepsin K to inhibit its function. Furthermore, the compounds RJC01981, KM08968 and SB01934 are represented to have promising anti-osteoporotic properties for the management of osteoporosis owing to their significantly well predicted ADMET properties.
引用
收藏
页码:2865 / 2880
页数:16
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