Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Cryo-EM reveals the architecture of placental malaria VAR2CSA and provides molecular insight into chondroitin sulfate binding

Research output: Contribution to journalJournal articleResearchpeer-review

  1. cyCombine allows for robust integration of single-cell cytometry datasets within and across technologies

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Modeling of waning immunity after SARS-CoV-2 vaccination and influencing factors

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Serum metabolome associated with severity of acute traumatic brain injury

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Structural basis for PoxtA-mediated resistance to phenicol and oxazolidinone antibiotics

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Structural basis of organic cation transporter-3 inhibition

    Research output: Contribution to journalJournal articleResearchpeer-review

View graph of relations

Placental malaria can have severe consequences for both mother and child and effective vaccines are lacking. Parasite-infected red blood cells sequester in the placenta through interaction between parasite-expressed protein VAR2CSA and the glycosaminoglycan chondroitin sulfate A (CS) abundantly present in the intervillous space. Here, we report cryo-EM structures of the VAR2CSA ectodomain at up to 3.1 Å resolution revealing an overall V-shaped architecture and a complex domain organization. Notably, the surface displays a single significantly electropositive patch, compatible with binding of negatively charged CS. Using molecular docking and molecular dynamics simulations as well as comparative hydroxyl radical protein foot-printing of VAR2CSA in complex with placental CS, we identify the CS-binding groove, intersecting with the positively charged patch of the central VAR2CSA structure. We identify distinctive conserved structural features upholding the macro-molecular domain complex and CS binding capacity of VAR2CSA as well as divergent elements possibly allowing immune escape at or near the CS binding site. These observations will support rational design of second-generation placental malaria vaccines.

Original languageEnglish
Article number2956
JournalNature Communications
Volume12
Issue number1
Pages (from-to)2956
ISSN2041-1722
DOIs
Publication statusPublished - 19 May 2021

    Research areas

  • Amino Acid Sequence, Antigens, Protozoan/chemistry, Chondroitin Sulfates/metabolism, Cryoelectron Microscopy, Female, Humans, Immune Evasion, Malaria, Falciparum/complications, Molecular Docking Simulation, Molecular Dynamics Simulation, Mutagenesis, Placenta/immunology, Plasmodium falciparum/genetics, Pregnancy, Pregnancy Complications, Parasitic/metabolism, Protein Binding, Protein Domains

ID: 75139586