Crystal structure and nanobodies against domain 3 of the malaria parasite fusogen Plasmodium falciparum HAP2

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Authors: Frankie M. T. Lyons, Jill Chmielewski, Li‐Jin Chan, Mikha Gabriela, Rainbow W.B. Chan, Amy Adair, Joshua Tong, Phillip Pymm, Kathleen Zeglinski, Quentin A. Gouil, Tham Wai-Hong, Melanie H. Dietrich
Cited by: 0
References: 49

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.

Fields of Study & Subjects

Malaria Research and Control Monoclonal and Polyclonal Antibodies Research Heat shock proteins research

Publication details

Journal / source
Biochemical Journal
Volume
483
Issue
2
Pages
119–133
Publication date
7 January 2026
Language
EN