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Pfs16:一种对疟原虫发育和传播至关重要的关键寄生泡膜蛋白。

Pfs16: A Key Parasitophorous Vacuole Membrane Protein Crucial for Malaria Parasite Development and Transmission.

作者信息

Shabani Sadeq, Serbus Laura Renee

机构信息

Department of Biological Sciences, Florida International University, 11200 SW 8 St, Miami, FL, 33199, USA.

出版信息

Protein J. 2025 Apr;44(2):133-146. doi: 10.1007/s10930-025-10260-1. Epub 2025 Feb 20.

DOI:10.1007/s10930-025-10260-1
PMID:39979562
Abstract

Malaria remains a formidable challenge to global health, claiming the lives of nearly half a million individuals annually despite vigorous efforts to curb its spread. Among the myriad factors influencing the persistence and virulence of this disease, the role of specific proteins during the Plasmodium development cycle is critical. The protein of interest, Pfs16, is a Parasitophorous Vacuole Membrane Protein expressed from the earliest asexual stages, which encompass the development of Plasmodium falciparum in the host, to the final stage of the parasite's development in the mosquito, the sporozoite, playing a crucial role in this lifecycle. Understanding the function and mechanism of this conserved protein is pivotal for advancing our strategies to combat malaria. In this review, we examine the work on Pfs16 in both the asexual and sexual stages of parasite development, aiming to gain a better understanding of this protein as a promising candidate for drug and vaccine development.

摘要

疟疾仍然是全球健康面临的一项严峻挑战,尽管人们为遏制其传播付出了巨大努力,但每年仍有近50万人死于疟疾。在影响这种疾病持续存在和毒力的众多因素中,特定蛋白质在疟原虫发育周期中的作用至关重要。我们感兴趣的蛋白质Pfs16是一种从最早的无性阶段就开始表达的寄生泡膜蛋白,这一阶段涵盖了恶性疟原虫在宿主体内的发育,直至寄生虫在蚊子体内发育的最后阶段——子孢子,它在这个生命周期中起着关键作用。了解这种保守蛋白质的功能和机制对于推进我们对抗疟疾的策略至关重要。在这篇综述中,我们研究了Pfs16在寄生虫发育的无性和有性阶段的研究工作,旨在更好地了解这种蛋白质,将其作为药物和疫苗开发的一个有前景的候选对象。

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本文引用的文献

1
Immunoinformatics design and synthesis of a multi-epitope vaccine against Helicobacter pylori based on lipid nanoparticles.基于脂质纳米粒的幽门螺杆菌多表位疫苗的免疫信息学设计与合成。
Sci Rep. 2024 Aug 2;14(1):17910. doi: 10.1038/s41598-024-68947-x.
2
Diversity and selection analyses identify transmission-blocking antigens as the optimal vaccine candidates in Plasmodium falciparum.多样性和选择分析将阻断传播的抗原确定为恶性疟原虫的最佳疫苗候选物。
EBioMedicine. 2024 Aug;106:105227. doi: 10.1016/j.ebiom.2024.105227. Epub 2024 Jul 16.
3
Development from Gametocyte to Oocyst: Insight from Functional Studies.
从配子体到卵囊的发育:功能研究的见解
Microorganisms. 2023 Jul 31;11(8):1966. doi: 10.3390/microorganisms11081966.
4
Targeting plasmodium α-tubulin-1 to block malaria transmission to mosquitoes.靶向疟原虫α-微管蛋白 1 阻断疟疾向蚊子传播。
Front Cell Infect Microbiol. 2023 Mar 16;13:1132647. doi: 10.3389/fcimb.2023.1132647. eCollection 2023.
5
RTS,S/AS01 malaria vaccine (Mosquirix): a profile of its use.RTS,S/AS01疟疾疫苗(Mosquirix):其使用概况
Drugs Ther Perspect. 2022;38(9):373-381. doi: 10.1007/s40267-022-00937-3. Epub 2022 Sep 7.
6
Evaluation of the Pfs25-IMX313/Matrix-M malaria transmission-blocking candidate vaccine in endemic settings.在流行地区评估 Pfs25-IMX313/Matrix-M 疟疾传播阻断候选疫苗。
Malar J. 2022 Jun 2;21(1):159. doi: 10.1186/s12936-022-04173-y.
7
Predicting epitopes for vaccine development using bioinformatics tools.使用生物信息学工具预测用于疫苗开发的表位。
Ther Adv Vaccines Immunother. 2022 May 21;10:25151355221100218. doi: 10.1177/25151355221100218. eCollection 2022.
8
The Cellular and Molecular Interaction Between Erythrocytes and Merozoites.红细胞与裂殖子之间的细胞和分子相互作用
Front Cell Infect Microbiol. 2022 Mar 31;12:816574. doi: 10.3389/fcimb.2022.816574. eCollection 2022.
9
Stressed Out About Gametocytogenesis.配子发生压力大。
Front Cell Infect Microbiol. 2021 Dec 2;11:790067. doi: 10.3389/fcimb.2021.790067. eCollection 2021.
10
Studies of the Parasite-Midgut Interaction Reveal Proteins Important for Malaria Transmission to Mosquitoes.寄生虫-中肠相互作用的研究揭示了与疟疾向蚊子传播相关的重要蛋白质。
Front Cell Infect Microbiol. 2021 Jun 28;11:654216. doi: 10.3389/fcimb.2021.654216. eCollection 2021.