Wan Fangping, Torres Marcelo D T, Peng Jacqueline, de la Fuente-Nunez Cesar
Machine Biology Group, Departments of Psychiatry and Microbiology, Institute for Biomedical Informatics, Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Departments of Bioengineering and Chemical and Biomolecular Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA.
Nat Biomed Eng. 2024 Jul;8(7):854-871. doi: 10.1038/s41551-024-01201-x. Epub 2024 Jun 11.
Molecular de-extinction aims at resurrecting molecules to solve antibiotic resistance and other present-day biological and biomedical problems. Here we show that deep learning can be used to mine the proteomes of all available extinct organisms for the discovery of antibiotic peptides. We trained ensembles of deep-learning models consisting of a peptide-sequence encoder coupled with neural networks for the prediction of antimicrobial activity and used it to mine 10,311,899 peptides. The models predicted 37,176 sequences with broad-spectrum antimicrobial activity, 11,035 of which were not found in extant organisms. We synthesized 69 peptides and experimentally confirmed their activity against bacterial pathogens. Most peptides killed bacteria by depolarizing their cytoplasmic membrane, contrary to known antimicrobial peptides, which tend to target the outer membrane. Notably, lead compounds (including mammuthusin-2 from the woolly mammoth, elephasin-2 from the straight-tusked elephant, hydrodamin-1 from the ancient sea cow, mylodonin-2 from the giant sloth and megalocerin-1 from the extinct giant elk) showed anti-infective activity in mice with skin abscess or thigh infections. Molecular de-extinction aided by deep learning may accelerate the discovery of therapeutic molecules.
分子复活旨在复活分子,以解决抗生素耐药性及其他当今的生物学和生物医学问题。在此我们表明,深度学习可用于挖掘所有已灭绝生物的蛋白质组,以发现抗生素肽。我们训练了由肽序列编码器与神经网络组成的深度学习模型集成,用于预测抗菌活性,并将其用于挖掘10,311,899个肽。这些模型预测出37,176个具有广谱抗菌活性的序列,其中11,035个在现存生物中未被发现。我们合成了69个肽,并通过实验证实了它们对细菌病原体的活性。与已知倾向于靶向细菌外膜的抗菌肽不同,大多数肽通过使细菌细胞质膜去极化来杀死细菌。值得注意的是,先导化合物(包括来自猛犸象的猛犸素-2、来自直牙象的象素-2、来自古代海牛的水豚素-1、来自巨型树懒的巨獭素-2和来自已灭绝的巨鹿的巨角鹿素-1)在患有皮肤脓肿或大腿感染的小鼠中显示出抗感染活性。深度学习辅助的分子复活可能会加速治疗性分子的发现。