易位
生物
内质网
疟疾
恶性疟原虫
疟原虫(生命周期)
转运蛋白
液泡
细胞生物学
顶复亚门
膜蛋白
寄生虫寄主
计算生物学
遗传学
细胞质
免疫学
膜
万维网
计算机科学
作者
Silvia Haase,Tania F. de Koning‐Ward
标识
DOI:10.1111/j.1462-5822.2010.01455.x
摘要
In order to survive and promote its virulence the malaria parasite must export hundreds of its proteins beyond an encasing vacuole and membrane into the host red blood cell. In the last few years, several major advances have been made that have significantly contributed to our understanding of this export process. These include: (i) the identification of sequences that direct protein export (a signal sequence and a motif termed PEXEL), which have allowed predictions of the exportomes of Plasmodium species that are the cause of malaria, (ii) the recognition that the fate of proteins destined for export is already decided within the parasite's endoplasmic reticulum and involves the PEXEL motif being recognized and cleaved by the aspartic protease plasmepsin V and (iii) the discovery of the Plasmodium translocon of exported proteins (PTEX) that is responsible for the passage of proteins across the vacuolar membrane. We review protein export in Plasmodium and these latest developments in the field that have now provided a new platform from which trafficking of malaria proteins can be dissected.
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