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保守肽序列与恶性疟原虫配子体表的肌动蛋白和烯醇酶结合。

Conserved peptide sequences bind to actin and enolase on the surface of Plasmodium berghei ookinetes.

机构信息

Centro de Investigación sobre Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Avenida Universidad No. 655, Col. Santa María Ahuacatitlán, Cuernavaca, Morelos, CP62508 México.

出版信息

Parasitology. 2011 Sep;138(11):1341-53. doi: 10.1017/S0031182011001296. Epub 2011 Aug 5.

Abstract

The description of Plasmodium ookinete surface proteins and their participation in the complex process of mosquito midgut invasion is still incomplete. In this study, using phage display, a consensus peptide sequence (PWWP) was identified in phages that bound to the Plasmodium berghei ookinete surface and, in selected phages, bound to actin and enolase in overlay assays with ookinete protein extracts. Actin was localized on the surface of fresh live ookinetes by immunofluorescence and electron microscopy using specific antibodies. The overall results indicated that enolase and actin can be located on the surface of ookinetes, and suggest that they could participate in Plasmodium invasion of the mosquito midgut.

摘要

疟原虫配子体表面蛋白的描述及其在蚊子中肠入侵的复杂过程中的作用尚不完全清楚。在这项研究中,我们使用噬菌体展示技术,从与疟原虫配子体表面结合的噬菌体中鉴定出一个保守肽序列(PWWP),并且在选定的噬菌体中,在与配子体蛋白提取物的覆盖试验中,与肌动蛋白和烯醇化酶结合。通过使用特异性抗体的免疫荧光和电子显微镜,在新鲜的活体配子体表面定位肌动蛋白。总的结果表明,烯醇化酶和肌动蛋白可以位于配子体的表面,并提示它们可能参与疟原虫入侵蚊子中肠。

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