Host-Pathogen Interactions and Structural Vaccinology Section, Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Laboratory of Membrane Proteins and Structural Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Nat Microbiol. 2021 Mar;6(3):380-391. doi: 10.1038/s41564-020-00858-9. Epub 2021 Jan 15.
Plasmodium falciparum VAR2CSA binds to chondroitin sulfate A (CSA) on the surface of the syncytiotrophoblast during placental malaria. This interaction facilitates placental sequestration of malaria parasites resulting in severe health outcomes for both the mother and her offspring. Furthermore, CSA is presented by diverse cancer cells and specific targeting of cells by VAR2CSA may become a viable approach for cancer treatment. In the present study, we determined the cryo-electron microscopy structures of the full-length ectodomain of VAR2CSA from P. falciparum strain NF54 in complex with CSA, and VAR2CSA from a second P. falciparum strain FCR3. The architecture of VAR2CSA is composed of a stable core flanked by a flexible arm. CSA traverses the core domain by binding within two channels and CSA binding does not induce major conformational changes in VAR2CSA. The CSA-binding elements are conserved across VAR2CSA variants and are flanked by polymorphic segments, suggesting immune selection outside the CSA-binding sites. This work provides paths for developing interventions against placental malaria and cancer.
恶性疟原虫 VAR2CSA 在胎盘疟疾期间与胎盘合胞滋养层表面的硫酸软骨素 A(CSA)结合。这种相互作用促进了疟疾寄生虫在胎盘内的定殖,导致母亲及其后代的严重健康后果。此外,CSA 存在于多种癌细胞表面,VAR2CSA 对细胞的特异性靶向可能成为癌症治疗的一种可行方法。在本研究中,我们确定了来自 P. falciparum 菌株 NF54 的全长外域的冷冻电子显微镜结构与 CSA 复杂的 VAR2CSA,以及来自第二种 P. falciparum 菌株 FCR3 的 VAR2CSA。VAR2CSA 的结构由稳定的核心组成,两侧是灵活的臂。CSA 通过结合在两个通道内穿过核心域,CSA 结合不会诱导 VAR2CSA 的主要构象变化。CSA 结合元件在 VAR2CSA 变体中是保守的,并且被多态性片段包围,这表明 CSA 结合位点之外存在免疫选择。这项工作为开发针对胎盘疟疾和癌症的干预措施提供了途径。