Structural insights into chondroitin sulfate binding in pregnancy-associated malaria

被引:9
|
作者
Khunrae, Pongsak [1 ]
Higgins, Matthew K. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
基金
英国惠康基金;
关键词
chondroitin sulfate; erythrocyte; Plasmodium falciparum; pregnancy-associated malaria; VAR2CSA; FALCIPARUM-INFECTED ERYTHROCYTES; INTERCELLULAR-ADHESION MOLECULE-1; PARASITE PLASMODIUM-FALCIPARUM; VARIANT SURFACE-ANTIGENS; HUMAN PLACENTA; BLOCKING ANTIBODIES; VAR GENES; MEMBRANE GLYCOPROTEIN; PROTECTIVE IMMUNITY; PROTEIN VAR2CSA;
D O I
10.1042/BST0381337
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malaria during pregnancy is caused when parasite-infected erythrocytes accumulate within the placenta through interactions between the VAR2CSA protein on the infected erythrocyte surface and placental CSPGs (chondroitin sulfate proteoglycans). This interaction is the major target for therapeutics to treat or prevent pregnancy-associated malaria. Here we review the structural characterization of CSPG-binding DBL (Duffy-binding like) domains from VAR2CSA and summarize the growing evidence that the exquisite ligand specificity of VAR2CSA results from the adoption of higher-order architecture in which these domains fold together to form a ligand-binding pocket.
引用
收藏
页码:1337 / 1341
页数:5
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