利用计算方法深入了解花粉过敏原 Bet v 1 的结构和结合研究。

In silico pharmacology Pub Date : 2025-01-11 eCollection Date: 2025-01-01 DOI:10.1007/s40203-024-00303-3
Mansi Pandit, Nandita Narayanasamy, N Latha
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引用次数: 0

摘要

Bet v 1,欧洲白桦树花粉过敏原是导致人类许多过敏反应的原因,如鼻炎、哮喘和口腔过敏综合征。该过敏原属于致病性相关(PR) 10类蛋白超家族,存在于几种自然发生的同种异构体中。关于betv1等过敏原和变异的有限结构信息促使我们进行它们的硅结构表征。在这项研究中,预测了Bet v1等过敏原的三维结构,然后将过敏原抗体与Bet v1特异性人IgE对接。此外,分子动力学模拟进行了过敏原抗体复合物。此外,在硅诱变设计低过敏性betv1变异进行。我们的研究旨在阐明基于结构特征的betv1等过敏原在引发过敏反应方面的差异能力,并确定了一个潜在的低过敏原,使我们能够提出它作为治疗桦树花粉诱导过敏的有希望的候选物。补充信息:在线版本提供补充资料,网址为10.1007/s40203-024-00303-3。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insights into structural and binding studies of pollen allergen Bet v 1 using computational approaches.

Bet v 1, the European White Birch tree pollen allergen is responsible for a number of allergic responses in humans such as rhinitis, asthma and oral allergy syndrome. The allergen belongs to pathogenesis-related (PR) class 10 protein superfamily and exists in several naturally occurring isoforms. Limited structural information on Bet v 1 isoallergens and variants prompted us to carry out their in silico structural characterization. In this study, three-dimensional structures of Bet v 1 isoallergens were predicted followed by allergen-antibody docking with Bet v 1- specific human IgE. Further, molecular dynamics simulations were performed for the allergen-antibody complexes. In addition, in silico mutagenesis was carried out for the design of a hypoallergenic variant of Bet v 1. Our study aimed to elucidate the differential ability of Bet v 1 isoallergens in eliciting allergic responses based on structural features and also identified a potential hypoallergen allowing us to propose it as a promising candidate for treating birch pollen-induced allergy.

Supplementary information: The online version contains supplementary material available at 10.1007/s40203-024-00303-3.

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