Inhibiting parasite proliferation using a rationally designed anti-tubulin agent.

ABSTRACT: Infectious diseases caused by apicomplexan parasites remain a global public health threat. The presence of multiple ligand-binding sites in tubulin makes this protein an attractive target for anti-parasite drug discovery. However, despite remarkable successes as anti-cancer agents, the rational development of protozoan parasite-specific tubulin drugs has been hindered by a lack of structural and biochemical information on protozoan tubulins. Here, we present atomic structures for a protozoan tubulin and microtubule and delineate the architectures of apicomplexan tubulin drug-binding sites. Based on this information, we rationally designed the parasite-specific tubulin inhibitor parabulin and show that it inhibits growth of parasites while displaying no effects on human cells. Our work pres

SUBMITTER: Gaillard N 

PROVIDER: S-EPMC8573600 | biostudies-literature | 2021 Nov

REPOSITORIES: biostudies-literature