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蛋白(PF3D7_1459400)在红细胞入侵过程中的定位和功能。

Localization and function of a protein (PF3D7_1459400) during erythrocyte invasion.

机构信息

West African Centre for Cell Biology of Infectious Pathogens, Department of Biochemistry, Cell and Molecular Biology, College of Basic and Applied Sciences, University of Ghana, Accra LG 54, Ghana.

Department of Biochemistry, Kogi State University, Anyigba P.M.B 1007, Nigeria.

出版信息

Exp Biol Med (Maywood). 2021 Jan;246(1):10-19. doi: 10.1177/1535370220961764. Epub 2020 Oct 5.

DOI:10.1177/1535370220961764
PMID:33019810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7797990/
Abstract

malaria is a global health problem. Erythrocyte invasion by merozoites appears to be a promising target to curb malaria. We have identified and characterized a novel protein that is involved in erythrocyte invasion. Our data on protein subcellular localization, stage-specific protein expression pattern, and merozoite invasion inhibition by α-peptide antibodies suggest a role for PF3D7_1459400 protein during erythrocyte invasion. Even more, the human immunoepidemiology data present PF3D7_1459400 protein as an immunogenic antigen which could be further exploited for the development of new anti-infective therapy against malaria.

摘要

疟疾是一个全球性的健康问题。疟原虫入侵红细胞似乎是抑制疟疾的一个有前途的靶点。我们已经鉴定和描述了一种参与红细胞入侵的新蛋白。我们关于蛋白亚细胞定位、阶段特异性蛋白表达模式以及α肽抗体对裂殖子入侵的抑制的数据表明,PF3D7_1459400 蛋白在红细胞入侵过程中发挥作用。更重要的是,人类免疫流行病学数据表明 PF3D7_1459400 蛋白是一种免疫原性抗原,可以进一步开发用于治疗疟疾的新抗感染疗法。

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本文引用的文献

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Protein S-Palmitoylation Is Responsive to External Signals and Plays a Regulatory Role in Microneme Secretion in Merozoites.蛋白质 S-棕榈酰化对外界信号有反应,并在裂殖子微线体分泌中起调节作用。
ACS Infect Dis. 2020 Mar 13;6(3):379-392. doi: 10.1021/acsinfecdis.9b00321. Epub 2020 Feb 14.
2
Plasmodium palmitoylation machinery engineered in for high-throughput screening of palmitoyl acyl-transferase inhibitors.用于棕榈酰基转移酶抑制剂高通量筛选的 中工程化的疟原虫棕榈酰化机制。
FEBS Open Bio. 2019 Jan 10;9(2):248-264. doi: 10.1002/2211-5463.12564. eCollection 2019 Feb.
3
Structure of Plasmodium falciparum Rh5-CyRPA-Ripr invasion complex.恶性疟原虫 Rh5-CyRPA-Ripr 入侵复合物的结构。
Nature. 2019 Jan;565(7737):118-121. doi: 10.1038/s41586-018-0779-6. Epub 2018 Dec 12.
4
Functional Characterization of Plasmodium falciparum Surface-Related Antigen as a Potential Blood-Stage Vaccine Target.恶性疟原虫表面相关抗原的功能特征分析——一种潜在的红内期疫苗靶标。
J Infect Dis. 2018 Jul 24;218(5):778-790. doi: 10.1093/infdis/jiy222.
5
Uncovering the essential genes of the human malaria parasite by saturation mutagenesis.通过饱和突变揭示人类疟疾寄生虫的必需基因。
Science. 2018 May 4;360(6388). doi: 10.1126/science.aap7847.
6
Plasmodium falciparum strains spontaneously switch invasion phenotype in suspension culture.恶性疟原虫株在悬浮培养中自发转换入侵表型。
Sci Rep. 2018 Apr 10;8(1):5782. doi: 10.1038/s41598-018-24218-0.
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Synergistic malaria vaccine combinations identified by systematic antigen screening.系统抗原筛选鉴定的协同疟疾疫苗组合。
Proc Natl Acad Sci U S A. 2017 Nov 7;114(45):12045-12050. doi: 10.1073/pnas.1702944114. Epub 2017 Oct 23.
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The Molecular Basis of Erythrocyte Invasion by Malaria Parasites.疟原虫对红细胞的入侵的分子基础。
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