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Plasmodium sporozoite phospholipid scramblase interacts with mammalian carbamoyl-phosphate synthetase 1 to infect hepatocytes
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Title
Plasmodium sporozoite phospholipid scramblase interacts with mammalian carbamoyl-phosphate synthetase 1 to infect hepatocytes
DGIST Authors
Cha, Sung-JaeKim, Min-SikNa, Chan HyunJacobs-Lorena, Marcelo
Issued Date
2021-11
Citation
Cha, Sung-Jae. (2021-11). Plasmodium sporozoite phospholipid scramblase interacts with mammalian carbamoyl-phosphate synthetase 1 to infect hepatocytes. doi: 10.1038/s41467-021-27109-7
Type
Article
Keywords
CIRCUMSPOROZOITE PROTEINMALARIA SPOROZOITESKUPFFER CELLSSURFACEFALCIPARUMCANDIDATEMEMBRANEEFFICACYPARASITEMATRIX
ISSN
2041-1723
Abstract
After inoculation by the bite of an infected mosquito, Plasmodium sporozoites enter the blood stream and infect the liver, where each infected cell produces thousands of merozoites. These in turn, infect red blood cells and cause malaria symptoms. To initiate a productive infection, sporozoites must exit the circulation by traversing the blood lining of the liver vessels after which they infect hepatocytes with unique specificity. We screened a phage display library for peptides that structurally mimic (mimotope) a sporozoite ligand for hepatocyte recognition. We identified HP1 (hepatocyte-binding peptide 1) that mimics a ~50 kDa sporozoite ligand (identified as phospholipid scramblase). Further, we show that HP1 interacts with a ~160 kDa hepatocyte membrane putative receptor (identified as carbamoyl-phosphate synthetase 1). Importantly, immunization of mice with the HP1 peptide partially protects them from infection by the rodent parasite P. berghei. Moreover, an antibody to the HP1 mimotope inhibits human parasite P. falciparum infection of human hepatocytes in culture. The sporozoite ligand for hepatocyte invasion is a potential novel pre-erythrocytic vaccine candidate. © 2021, The Author(s).
URI
http://hdl.handle.net/20.500.11750/15919
DOI
10.1038/s41467-021-27109-7
Publisher
Nature Research
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김민식
Kim, Min-Sik김민식

Department of New Biology

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