Computational resources: a regulatory need, a tool for research.

Renato Truffer, Michael B Stadler, Monique Vogel, Adriano Mari, Beda M Stadler
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Abstract

Background: We have recently reported a new method based on protein motifs to predict allergenicity by protein sequence. By using the more complete allergen database Allergome (www.allergome.org), as the basis for the motif identification process, we obtained a new set of allergenic motifs. We studied whether an allergenic motif may be used instead of a full length allergen for predicting allergenicity.

Methods: Sequence accession numbers of allergens were received from A. Mari of the Allergome Project. The sequences were downloaded and integrated in the allergen database, which was used to produce new motifs applicable for allergenicity prediction. The motif containing allergenic tropomyosins of different non vertebrate species was chosen. A consensus sequence of the tropomyosin motif was synthesized and expressed in Escherichia coli (E. coli). The purified peptide was analyzed for specificity with enzyme linked-immunosorbent assay (ELISA).

Results: Based on the Allergome dataset, we calculated 69 motifs containing 912 sequences. Prediction performance of this new set of allergenic motifs is increased compared to the original 52 motifs. The IgE immunological reactivity of the recombinant tropomyosin motif was comparable to that obtained with a full length recombinant shrimp tropomyosin (rPen a 1) tested in the ImmunoCAP system.

Discussion: The use of the motif-based allergenicity prediction method is more accurate than the guidelines proposed by FAO/WHO, however continuous updates of the motif dataset are necessary to guarantee a high prediction performance of this method. The experiments performed with the tropomyosin motif showed that peptides based on the consensus sequence of motifs may represent the allergenic epitope, which can be used in future diagnostic or therapeutic approaches.

计算资源:监管需要,研究工具。
背景:我们最近报道了一种基于蛋白质基序的新方法,通过蛋白质序列预测过敏原。利用较为完整的过敏原数据库Allergome (www.allergome.org)作为基序鉴定过程的基础,我们获得了一组新的致敏基序。我们研究了是否可以使用致敏基序代替全长过敏原来预测致敏性。方法:从A. Mari过敏原项目中获取过敏原的序列加入号。这些序列被下载并整合到过敏原数据库中,用于产生新的基序,适用于过敏原预测。选取了含有不同非脊椎动物致敏原肌球蛋白的基序。合成了原肌球蛋白基序的一致序列,并在大肠杆菌中表达。用酶联免疫吸附试验(ELISA)分析纯化肽的特异性。结果:基于Allergome数据集,我们计算出69个motif,包含912个序列。与原来的52个基序相比,这组新的过敏原基序的预测性能有所提高。重组原肌球蛋白基序的IgE免疫反应性与在ImmunoCAP系统中测试的全长重组虾原肌球蛋白(rPen a1)相当。讨论:使用基于基序的过敏原预测方法比FAO/WHO提出的指南更准确,但是为了保证该方法的高预测性能,需要不断更新基序数据集。用原肌球蛋白基序进行的实验表明,基于基序共识序列的肽可能代表过敏原表位,这可以用于未来的诊断或治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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