Institut Pasteur Paris, UTechS-PBI/Imagopole, 25-28 rue du Docteur Roux, 75015, France.
Institut Pasteur Korea, 16 Daewangpangyo-ro 712 beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13488, Republic of Korea.
Trends Parasitol. 2019 Jul;35(7):559-570. doi: 10.1016/j.pt.2019.05.004. Epub 2019 Jun 5.
Cell-based phenotypic screening has proven to be valuable, notably in recapitulating relevant biological conditions, for example, the host cell/pathogen niche. However, the corresponding methodological complexity is not readily compatible with high-throughput pipelines, and fails to inform either molecular target or mechanism of action, which frustrates conventional drug-discovery roadmaps. We review the state-of-the-art and emerging technologies that suggest new strategies for harnessing value from the complexity of phenotypic screening and augmenting powerful utility for translational drug discovery. Advances in cellular, molecular, and bioinformatics technologies are converging at a cutting edge where the complexity of phenotypic screening may no longer be considered a hinderance but rather a catalyst to chemotherapeutic discovery for infectious diseases.
基于细胞的表型筛选已被证明具有价值,特别是在再现相关生物学条件方面,例如宿主细胞/病原体生态位。然而,相应的方法学复杂性不容易与高通量管道兼容,并且无法提供分子靶标或作用机制的信息,这阻碍了传统的药物发现路线图。我们回顾了最先进的和新兴的技术,这些技术为利用表型筛选的复杂性并增强转化药物发现的强大功能提供了新的策略。细胞、分子和生物信息学技术的进步正在融合的前沿,在这个前沿,表型筛选的复杂性不再被认为是障碍,而是传染病化学治疗发现的催化剂。