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疟原虫裂殖子表面蛋白 119 的结构、抗体特异性及其对疟疾疫苗设计的影响。

The structure of Plasmodium yoelii merozoite surface protein 119, antibody specificity and implications for malaria vaccine design.

机构信息

Divisions of Parasitology, MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.

出版信息

Open Biol. 2014 Jan 8;4(1):130091. doi: 10.1098/rsob.130091.

Abstract

Merozoite surface protein 1 (MSP1) has been identified as a target antigen for protective immune responses against asexual blood stage malaria, but effective vaccines based on MSP1 have not been developed so far. We have modified the sequence of Plasmodium yoelii MSP119 (the C-terminal region of the molecule) and examined the ability of the variant proteins to bind protective monoclonal antibodies and to induce protection by immunization. In parallel, we examined the structure of the protein and the consequences of the amino acid changes. Naturally occurring sequence polymorphisms reduced the binding of individual protective antibodies, indicating that they contribute to immune evasion, but immunization with these variant proteins still provided protective immunity. One variant that resulted in the localized distortion of a loop close to the N-terminus of MSP119 almost completely ablated protection by immunization, indicating the importance of this region of MSP119 as a target for protective immunity and in vaccine development.

摘要

裂殖子表面蛋白 1(MSP1)已被确定为针对无性血期疟疾的保护性免疫反应的靶抗原,但迄今为止尚未开发出基于 MSP1 的有效疫苗。我们已经修饰了约氏疟原虫 MSP119 的序列(分子的 C 末端区域),并研究了变异蛋白结合保护性单克隆抗体的能力和免疫接种诱导保护的能力。同时,我们还研究了该蛋白的结构以及氨基酸变化的后果。天然存在的序列多态性降低了个别保护性抗体的结合,表明它们有助于免疫逃避,但用这些变异蛋白免疫接种仍提供了保护性免疫。一个导致 MSP119 N 端附近一个环局部扭曲的变异体几乎完全消除了免疫接种的保护作用,这表明 MSP119 的这一区域作为保护性免疫和疫苗开发的靶标非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc4/3909271/9b8dfa76a78e/rsob-4-130091-g1.jpg

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