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牛β-和κ-酪蛋白的遗传变异导致体外胃肠消化后不同的免疫球蛋白 E 结合表位。

Genetic variants of bovine β- and κ-casein result in different immunoglobulin E-binding epitopes after in vitro gastrointestinal digestion.

机构信息

Department of Animal Breeding and Genetics, Justus-Liebig University, 35390 Gießen, Germany.

出版信息

J Dairy Sci. 2013 Sep;96(9):5532-43. doi: 10.3168/jds.2013-6684. Epub 2013 Jul 17.

Abstract

Immunoglobulin E-mediated allergy to cow milk is a common allergy in industrialized countries, mainly affecting young children and infants. β-Casein (CN) and κ-CN belong to the major allergens in cow milk. Within these milk proteins, genetic polymorphisms occur, which are characterized by substitutions or deletions of AA, resulting in different variants for each protein. Until now, these variants have not been considered when discussing the allergenic potential of bovine milk. In this study, the focus was placed on the arising peptide pattern after in vitro gastrointestinal digestion of several β- and κ-CN variants to determine resistant fragments containing IgE-binding epitopes and to identify potential differences between these variants. β-Casein A(1), A(2), and B, as well as κ-CN A, B, and E, were separated and isolated from milk of cows homozygous for these variants and digested with an in vitro gastrointestinal digestion model. The resulting peptides were identified using mass spectrometry and compared with previously determined epitopes. Seven β-CN and 4 κ-CN peptides, common in all β- or κ-CN variants, remained of sufficient size to harbor IgE-binding epitopes. In addition, some peptides and, consequently, epitopes differ from each other due to the AA substitution occurring in the individual variants. The distinct peptides AA 108 to 129 of β-CN A(1) and A(2), AA 103 to 123 of β-CN B, as well as AA 59 to 72, AA 59 to 80, and AA 58 to 80 of all 3 β-CN variants correspond to the IgE-binding epitopes AA 107 to 120 and AA 55 to 70, respectively. In κ-CN, the 2 variant-specific peptides AA 136 to 149 (κ-CN A, E) and AA 134 to 150 (κ-CN B) are congruent with the IgE-binding epitope AA 137 to 148. The present study shows that genetic polymorphisms affected the arising peptide pattern of the caseins and thus modifications in the IgE-binding epitopes occurred. As a consequence, the casein variants could show differences in their allergenicity. Studies investigating the allergenic potential of these different peptides are currently in progress.

摘要

免疫球蛋白 E 介导的牛奶过敏是工业化国家常见的过敏,主要影响幼儿和婴儿。β-酪蛋白(CN)和κ-CN 属于牛奶中的主要过敏原。在这些牛奶蛋白中,存在遗传多态性,其特征是 AA 的取代或缺失,导致每种蛋白都有不同的变体。到目前为止,在讨论牛乳的变应原性时,还没有考虑到这些变体。在这项研究中,重点放在体外胃肠道消化几种β-和κ-CN 变体后产生的肽模式上,以确定含有 IgE 结合表位的抗性片段,并确定这些变体之间的潜在差异。从这些变体纯合的牛奶中分离和分离出β-酪蛋白 A(1)、A(2)和 B,以及 κ-CN A、B 和 E,并使用体外胃肠道消化模型进行消化。使用质谱法鉴定产生的肽,并与先前确定的表位进行比较。七种β-CN 和四种κ-CN 肽在所有β-或κ-CN 变体中都很常见,其大小足以保持 IgE 结合表位。此外,由于个别变体中发生的 AA 取代,一些肽和相应的表位彼此不同。β-CN A(1)和 A(2)的 AA 108 到 129、β-CN B 的 AA 103 到 123 以及所有 3 种β-CN 变体的 AA 59 到 72、AA 59 到 80 和 AA 58 到 80 的独特肽对应于 IgE 结合表位 AA 107 到 120 和 AA 55 到 70。在 κ-CN 中,2 种变体特异性肽 AA 136 到 149(κ-CN A,E)和 AA 134 到 150(κ-CN B)与 IgE 结合表位 AA 137 到 148 一致。本研究表明,遗传多态性影响了酪蛋白的产生肽模式,从而导致 IgE 结合表位发生修饰。因此,酪蛋白变体可能在其变应原性方面存在差异。目前正在进行研究这些不同肽的变应原性潜力的研究。

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