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来自嗜卷书虱的原肌球蛋白的克隆与特性分析

Cloning and characterization of tropomyosin from the mite Chortoglyphus arcuatus.

作者信息

López-Matas M Angeles, Iraola Victor, Moya Raquel, Vailes Lisa D, Pomés Anna, Boquete Manuel, Fernández-Caldas Enrique, Arlian L G, Chapman Martin, Carnés Jerónimo

机构信息

R&D Department, Laboratorios LETI, S.L. C/del Sol 5, Tres Cantos, Madrid 28760, Spain.

Basic Research, Indoor Biotechnologies Inc., Charlottesville, VA, USA.

出版信息

Mol Immunol. 2015 Dec;68(2 Pt C):634-40. doi: 10.1016/j.molimm.2015.10.004. Epub 2015 Oct 29.

Abstract

Tropomyosin is a pan-allergen that shares a high homology among species. It is involved in cross-reactivity among mites, crustaceans, mollusks and insects. The objectives were to express and purify recombinant tropomyosin from the storage mite Chortoglyphus arcuatus, and to investigate the homology and cross-reactivity with tropomyosin from other invertebrates. Recombinant C. arcuatus tropomyosin (r-Cho a 10) was selected from a library by screening with a pool of patient sera. r-Cho a 10 (UniProt: H2DFL1) was sequenced, expressed in Escherichia coli and purified by ion exchange and affinity chromatography. Polyclonal anti-tropomyosin antibodies were produced in mice. IgE recognition of r-Cho a 10 was checked by immunoblot. Immunoblot inhibition assays were used to identify the native tropomyosin in the complete extract from C. arcuatus and study cross-reactivity between r-Cho a 10 and Der p 10. Identification of tropomyosin in other allergenic sources was performed by immunoblot. r-Cho a 10 showed a high homology (54-96%) with other tropomyosins from different allergenic sources. IgE recognition was observed using a pool of sera from sensitized individuals. Tropomyosins from different extracts were identified not only in the whole C. arcuatus extract but also in Dermatophagoides pteronyssinus, shrimp, mussel, cockroach and Anisakis extracts with polyclonal α-Cho a 10. r-Cho a 10 completely inhibited the recognition of Der p 10. Recombinant C. arcuatus tropomyosin maintained its capacity to recognize IgE. r-Cho a 10 was used to prove cross-reactivity among tropomyosins from other invertebrate species, including mites. This is the first C. arcuatus allergen included in the WHO/IUIS (World Health Organization/International Union of Immunological Societies) Allergen Nomenclature database.

摘要

原肌球蛋白是一种泛过敏原,在物种间具有高度同源性。它参与螨类、甲壳类、软体动物和昆虫之间的交叉反应。目的是表达和纯化来自储藏螨嗜卷书虱的重组原肌球蛋白,并研究其与其他无脊椎动物原肌球蛋白的同源性和交叉反应性。通过用患者血清池筛选从文库中选出重组嗜卷书虱原肌球蛋白(r-Cho a 10)。对r-Cho a 10(UniProt:H2DFL1)进行测序,在大肠杆菌中表达,并通过离子交换和亲和层析进行纯化。在小鼠体内产生多克隆抗原肌球蛋白抗体。通过免疫印迹检查r-Cho a 10的IgE识别情况。免疫印迹抑制试验用于鉴定嗜卷书虱完整提取物中的天然原肌球蛋白,并研究r-Cho a 10与Der p 10之间的交叉反应性。通过免疫印迹对其他过敏原来源中的原肌球蛋白进行鉴定。r-Cho a 10与来自不同过敏原来源的其他原肌球蛋白显示出高度同源性(54-96%)。使用来自致敏个体的血清池观察到IgE识别情况。用多克隆α-Cho a 10不仅在嗜卷书虱的完整提取物中,而且在粉尘螨、虾、贻贝、蟑螂和异尖线虫提取物中鉴定出不同提取物中的原肌球蛋白。r-Cho a 10完全抑制了对Der p 10的识别。重组嗜卷书虱原肌球蛋白保持了其识别IgE的能力。r-Cho a 10被用于证明来自其他无脊椎动物物种(包括螨类)原肌球蛋白之间的交叉反应性。这是世界卫生组织/国际免疫学会(WHO/IUIS)过敏原命名数据库中收录的首个嗜卷书虱过敏原。

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