Food Toxicology Division, Indian Institute of Toxicology Research, Council of Scientific and Industrial Research, Lucknow, Uttar Pradesh, India.
Immunopharmacol Immunotoxicol. 2011 Sep;33(3):410-22. doi: 10.3109/08923973.2010.523704. Epub 2010 Oct 21.
Development of genetically modified (GM) crops is on increase to improve food quality, increase harvest yields, and reduce the dependency on chemical pesticides. Before their release in marketplace, they should be scrutinized for their safety. Several guidelines of different regulatory agencies like ILSI, WHO Codex, OECD, and so on for allergenicity evaluation of transgenics are available and sequence homology analysis is the first test to determine the allergenic potential of inserted proteins. Therefore, to test and validate, 312 allergenic, 100 non-allergenic, and 48 inserted proteins were assessed for sequence similarity using 8-mer, 80-mer, and full FASTA search. On performing sequence homology studies, ~94% the allergenic proteins gave exact matches for 8-mer and 80-mer homology. However, 20 allergenic proteins showed non-allergenic behavior. Out of 100 non-allergenic proteins, seven qualified as allergens. None of the inserted proteins demonstrated allergenic behavior. In order to improve the predictability, proteins showing anomalous behavior were tested by Algpred and ADFS separately. Use of Algpred and ADFS softwares reduced the tendency of false prediction to a great extent (74-78%). In conclusion, routine sequence homology needs to be coupled with some other bioinformatic method like ADFS/Algpred to reduce false allergenicity prediction of novel proteins.
转基因作物的发展旨在提高食品质量、增加收成、减少对化学农药的依赖。在投放市场之前,应对其安全性进行仔细审查。国际生命科学学会(ILSI)、世界卫生组织食品法典委员会(WHO Codex)、经济合作与发展组织(OECD)等不同监管机构都制定了转基因生物过敏性评估指南,序列同源性分析是确定插入蛋白过敏性潜力的首要测试。因此,为了进行测试和验证,使用 8 -mer、80-mer 和完整 FASTA 搜索对 312 种过敏原蛋白、100 种非过敏原蛋白和 48 种插入蛋白进行了序列相似性评估。进行序列同源性研究时,约 94%的过敏原蛋白在 8-mer 和 80-mer 同源性上完全匹配。然而,有 20 种过敏原蛋白表现出非过敏原行为。在 100 种非过敏原蛋白中,有 7 种被鉴定为过敏原。没有插入蛋白表现出过敏原行为。为了提高预测的准确性,对表现出异常行为的蛋白分别使用了 Algpred 和 ADFS 进行了测试。Algpred 和 ADFS 软件的使用在很大程度上降低了错误预测的趋势(74-78%)。总之,常规序列同源性需要与其他生物信息学方法(如 ADFS/Algpred)相结合,以减少对新型蛋白的错误过敏原性预测。