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Malaria is a deadly infectious disease primarily caused by the parasite Plasmodium falciparum . It remains a major global health problem, and there is no highly effective vaccine. A parasite protein called RH5 is centrally involved in the invasion of host red blood cells, making it—and the other parasite proteins it interacts with—promising vaccine targets. We recently identified a protein called P113 that binds RH5, suggesting that it anchors RH5 to the parasite surface. In this paper, we use structural biology to locate and characterize the RH5 binding region on P113. These findings will be important to guide the development of new antimalarial vaccines to ultimately prevent this disease, which affects some of the poorest people on the planet.

Original publication

DOI

10.1128/mbio.01566-20

Type

Journal article

Journal

mBio

Publisher

American Society for Microbiology

Publication Date

27/10/2020

Volume

11