Crystal structure and nanobodies against domain 3 of the malaria parasite fusogen Plasmodium falciparum HAP2
Authors:
- Frankie M. T. LyonsFLFrankie M. T. Lyons
- Jill ChmielewskiJCJill Chmielewski
- Li-Jin ChanLCLi-Jin Chan
- Mikha GabrielaMGMikha Gabriela
- Rainbow W. B. ChanRCRainbow W. B. Chan
- Amy AdairAAAmy Adair
- Joshua TongJTJoshua Tong
- Phillip PymmPPPhillip Pymm
- Kathleen ZeglinskiKZKathleen Zeglinski
- Quentin GouilQGQuentin Gouil
- Wai-Hong ThamWTWai-Hong Tham
- Melanie H. DietrichMDMelanie H. Dietrich
Preprint
Abstract
Malaria parasites are transmitted to humans through a bite from an infected female Anopheles mosquito. Within the mosquito midgut, malaria parasite gametes are activated and undergo fertilisation. If parasite fertilisation is perturbed, this stops the transmission of malaria parasites from mosquito to human. One proposed target of transmission-blocking interventions is Plasmodium falciparum fusogen PfHAP2, which is essential for gamete fusion during parasite fertilisation. However, to date, no monoclonal antibodies or structures of PfHAP2 have been generated. We have identified nanobodies that bind specifically to domain 3 of PfHAP2 with nanomolar affinities, two of which show some cross-species reactivity with HAP2 of other Plasmodium species. The crystal structure of one nanobody in complex with domain 3 of PfHAP2 provides the first structural insights into this transmission-blocking target in P. falciparum .Keywords
All Related Versions
- Published version: Biochemical Journal, 483 (2), 119.
Funding Information
- National Health and Medical Research Council (GNT2016908)
- National Health and Medical Research Council (GNT2001385)
- National Health and Medical Research Council (GNT2007996)
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