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疟原虫的致命弱点:功能相关的入侵结构

The Malaria Parasite's Achilles' Heel: Functionally-relevant Invasion Structures.

作者信息

Patarroyo Manuel E, Alba Martha P, Reyes Cesar, Rojas-Luna Rocio, Patarroyo Manuel A

机构信息

Fundación Instituto de Inmunologia de Colombia (FIDIC), Bogota, Colombia.

出版信息

Curr Issues Mol Biol. 2016;18:11-9. Epub 2015 Apr 1.

Abstract

Malaria parasites have their Achilles' heel; they are vulnerable in small parts of their relevant molecules where they can be wounded and killed. These are sporozoite and merozoite protein conserved high activity binding peptides (cHABPs), playing a critical role in binding to and invasion of host cells (hepatocytes and erythrocytes, respectively). cHABPs can be modified by specific amino acid replacement, according to previously published physicochemical rules, to produce analogues (mHABPs) having left-handed polyproline II (PPIIL)-like structures which can modulate an immune response due to fitting perfectly into the HLA-DRβ1* peptide binding region (PBR) and having an appropriate presentation to the T-cell receptor (TCR).

摘要

疟原虫有其致命弱点;它们在相关分子的小部分区域较为脆弱,在这些区域它们可能会受到损伤并被杀死。这些是子孢子和裂殖子蛋白保守高活性结合肽(cHABP),分别在与宿主细胞(肝细胞和红细胞)结合及侵入宿主细胞过程中起关键作用。根据先前发表的物理化学规则,cHABP可通过特定氨基酸置换进行修饰,以产生具有左手多聚脯氨酸II(PPIIL)样结构的类似物(mHABP),这些类似物可通过完美契合HLA - DRβ1*肽结合区域(PBR)并向T细胞受体(TCR)进行适当呈递来调节免疫反应。

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