Suppr超能文献

高通量测量刚地弓形虫微线体分泌。

High-Throughput Measurement of Microneme Secretion in Toxoplasma gondii.

机构信息

Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Methods Mol Biol. 2020;2071:157-169. doi: 10.1007/978-1-4939-9857-9_9.

Abstract

Micronemes are specialized secretory organelles present in all motile forms of apicomplexan parasites. Microneme vesicles hold adhesins and other proteins that are secreted to facilitate parasite attachment, invasion of host cells, and egress following replication-all processes indispensable for cell-to-cell transmission of these obligate intracellular parasites. Defining the signaling pathways that lead to microneme secretion is an important part of understanding the infectious cycle of apicomplexan parasites. However, the classical method of measuring microneme secretion by immunoblotting for microneme proteins in parasite excreted/secreted antigen (ESA) preparations is low-throughput and only semiquantitative. We recently reported a new luciferase-based method for measuring microneme secretion in a 96-well format with high sensitivity in the model apicomplexan Toxoplasma gondii. Here, we aim to elaborate on this detection method and review current practices for stimulating microneme secretion in vitro.

摘要

微绒毛是所有能动形式的顶复门寄生虫中特化的分泌细胞器。微绒毛囊泡含有黏附素和其他分泌蛋白,这些蛋白有助于寄生虫附着、入侵宿主细胞以及复制后的逸出——所有这些过程对于这些必需的细胞内寄生虫的细胞间传播都是不可或缺的。确定导致微绒毛分泌的信号通路是理解顶复门寄生虫感染周期的重要部分。然而,通过免疫印迹检测寄生虫排泄/分泌抗原(ESA)制剂中的微绒毛蛋白来测量微绒毛分泌的经典方法是低通量的,并且只是半定量的。我们最近报道了一种新的基于荧光素酶的方法,用于在 96 孔格式中以高灵敏度测量模型顶复门寄生虫弓形虫中的微绒毛分泌。在这里,我们旨在详细阐述这种检测方法,并回顾目前在体外刺激微绒毛分泌的实践。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验