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6AZX

Crystal structure of the neutralizing anti-circumsporozoite protein 663 antibody

Summary for 6AZX
Entry DOI10.2210/pdb6azx/pdb
Related5BK0 5BK3 5BK5 6AZM
Descriptor663 antibody, heavy chain, 663 antibody, light chain (3 entities in total)
Functional Keywordsmalaria, circumsporozoite protein, fab, immune system
Biological sourceHomo sapiens (Human)
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Total number of polymer chains4
Total formula weight95759.21
Authors
Scally, S.W.,Bosch, A.,Triller, G.,Wardemann, H.,Julien, J.P. (deposition date: 2017-09-13, release date: 2017-12-13, Last modification date: 2024-11-13)
Primary citationTriller, G.,Scally, S.W.,Costa, G.,Pissarev, M.,Kreschel, C.,Bosch, A.,Marois, E.,Sack, B.K.,Murugan, R.,Salman, A.M.,Janse, C.J.,Khan, S.M.,Kappe, S.H.I.,Adegnika, A.A.,Mordmuller, B.,Levashina, E.A.,Julien, J.P.,Wardemann, H.
Natural Parasite Exposure Induces Protective Human Anti-Malarial Antibodies.
Immunity, 47:1197-1209.e10, 2017
Cited by
PubMed Abstract: Antibodies against the NANP repeat of circumsporozoite protein (CSP), the major surface antigen of Plasmodium falciparum (Pf) sporozoites, can protect from malaria in animal models but protective humoral immunity is difficult to induce in humans. Here we cloned and characterized rare affinity-matured human NANP-reactive memory B cell antibodies elicited by natural Pf exposure that potently inhibited parasite transmission and development in vivo. We unveiled the molecular details of antibody binding to two distinct protective epitopes within the NANP repeat. NANP repeat recognition was largely mediated by germline encoded and immunoglobulin (Ig) heavy-chain complementarity determining region 3 (HCDR3) residues, whereas affinity maturation contributed predominantly to stabilizing the antigen-binding site conformation. Combined, our findings illustrate the power of exploring human anti-CSP antibody responses to develop tools for malaria control in the mammalian and the mosquito vector and provide a molecular basis for the structure-based design of next-generation CSP malaria vaccines.
PubMed: 29195810
DOI: 10.1016/j.immuni.2017.11.007
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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