Paul Vijay, Steinke Kerstin, Meyer Heinrich H D
Physiology Weihenstephan, Technical University Munich, Weihenstephaner Berg 3, 85350 Freising, Germany.
Anal Chim Acta. 2008 Jan 21;607(1):106-13. doi: 10.1016/j.aca.2007.11.022. Epub 2007 Nov 19.
The increasing global adoption of genetically modified (GM) plant derivatives in animal feed has provoked a strong demand for an appropriate detection method to evaluate the existence of transgenic protein in animal tissues and animal by-products derived from GM plant fed animals. A highly specific and sensitive sandwich enzyme immunoassay for the surveillance of transgenic Cry1Ab protein from Bt-maize in the blood plasma of cows fed on Bt-maize was developed and validated according to the criteria of EU-Decision 2002/657/EC. The sandwich assay is based on immuno-affinity purified polyclonal antibody raised against Cry1Ab protein in rabbits. Native and biotinylated forms of this antibody served as capture antibody and detection antibody for the ELISA, respectively. Streptavidin-horseradish peroxidase conjugate and TMB substrate provided the means for enzymatic colour development. The immunoassay allowed Cry1Ab protein determination in bovine blood plasma in an analytical range of 0.4-100 ng mL(-1) with a decision limit (CCalpha) of 1.5 ng mL(-1) and detection capability (CCbeta) of 2.3 ng mL(-1). Recoveries ranged from 89 to 106% (mean value of 98%) in spiked plasma. In total, 20 plasma samples from cows (n=7) fed non-transgenic maize and 24 samples from cows (n=8) fed transgenic maize (collected before and, after 1 and 2 months of feeding) were investigated for the presence of the Cry1Ab protein. There was no difference amongst both groups (all the samples were below 1.5 ng mL(-1); CCalpha). No plasma sample was positive for the presence of the Cry1Ab protein at CCalpha and CCbeta of the assay.
全球范围内,动物饲料中越来越多地采用转基因植物衍生物,这引发了对一种合适检测方法的强烈需求,以评估源自食用转基因植物的动物的组织和动物副产品中转基因蛋白的存在情况。根据欧盟第2002/657/EC号决定的标准,开发并验证了一种高度特异性和灵敏的夹心酶免疫测定法,用于监测食用转基因玉米的奶牛血浆中的转基因Cry1Ab蛋白。该夹心测定法基于在兔体内产生的针对Cry1Ab蛋白的免疫亲和纯化多克隆抗体。该抗体的天然形式和生物素化形式分别用作ELISA的捕获抗体和检测抗体。链霉亲和素 - 辣根过氧化物酶共轭物和TMB底物提供了酶促显色的手段。该免疫测定法能够在0.4 - 100 ng mL(-1)的分析范围内测定牛血浆中的Cry1Ab蛋白,决策限(CCalpha)为1.5 ng mL(-1),检测能力(CCbeta)为2.3 ng mL(-1)。加标血浆中的回收率在89%至106%之间(平均值为98%)。总共对20份来自食用非转基因玉米的奶牛(n = 7)的血浆样本和24份来自食用转基因玉米的奶牛(n = 8)的血浆样本(在喂食前、喂食1个月和2个月后采集)进行了Cry1Ab蛋白存在情况调查。两组之间没有差异(所有样本均低于1.5 ng mL(-1);CCalpha)。在该测定法的CCalpha和CCbeta水平下,没有血浆样本的Cry1Ab蛋白检测呈阳性。