Machine learning approaches to optimize small-molecule inhibitors for RNA targeting

In the era of data science, data-driven algorithms have emerged as powerful platforms that can consolidate bioisosteric rules for preferential modifications on small molecules with a common molecular scaffold. Here we present complementary data-driven algorithms to minimize the search in chemical space for phenylthiazole-containing molecules that bind the RNA hairpin within the ribosomal peptidyl transferase center (PTC) of Mycobacterium tuberculosis. Our results indicate visual, geometrical, and chemical features that enhance the binding to the targeted RNA. Functional validation was conducted after synthesizing 10 small molecules pinpointed computationally. Four of the 10 were found to be potent inhibitors that target hairpin 91 in the ribosomal PTC of M. tuberculosis and, as a result, stop translation.

Automated summary

In this study, data-driven algorithms were employed to identify phenylthiazole-containing molecules that can bind to the RNA hairpin of Mycobacterium tuberculosis. Functional validation of computationally selected molecules resulted in the discovery of potent inhibitors targeting the ribosomal peptidyl transferase center.