作者
Mohammad Ghazi Vakili,Christoph Gorgulla,Jamie Snider,AkshatKumar Nigam,Dmitry S. Bezrukov,Daniel Varoli,Alex Aliper,Daniil Polykovskiy,Krishna Mohan Das,Huel Cox,Anna Lyakisheva,Ardalan Hosseini Mansob,Zhong Yao,L. Bitar,Danielle Tahoulas,Dora Čerina,Eugene V. Radchenko,Xiao Ding,Jinxin Liu,Fanye Meng,Feng Ren,Yudong Cao,Igor Štagljar,Alán Aspuru‐Guzik,Alex Zhavoronkov
摘要
We introduce a quantum–classical generative model for small-molecule design, specifically targeting KRAS inhibitors for cancer therapy. We apply the method to design, select and synthesize 15 proposed molecules that could notably engage with KRAS for cancer therapy, with two holding promise for future development as inhibitors. This work showcases the potential of quantum computing to generate experimentally validated hits that compare favorably against classical models. A hybrid model combines quantum and classical approaches to generate compounds targeting the KRAS protein.