Suonpää M, Markela E, Ståhlberg T, Hemmilä I
Wallac Oy, Turku, Finland.
J Immunol Methods. 1992 May 18;149(2):247-53. doi: 10.1016/0022-1759(92)90256-s.
Labelling of streptavidin with a fluorogenic europium ion was optimized with the aim of obtaining a universal, stable and highly sensitive non-isotopic label for time-resolved fluorometric immunoassays (TR-FIA) based on dissociative fluorescence enhancement (DELFIA). Even the conjugation of all the free amino groups of streptavidin with Eu chelates had only a minor effect on the binding capacity of the protein or its affinity. The labelled streptavidin was evaluated in indirect time-resolved immunofluorometric assays of human follicle and thyroid stimulating hormones (FSH and TSH). The interassay imprecision was below 3% within the concentration range from 2.5 to 94 U/l for the FSH samples and below 5% in the range from 2.4 to 35 mIU/l for the TSH samples. The detection limits of the assays for FSH and TSH were 0.05-0.10 U/l and 0.01-0.025 mIU/l, respectively, when a CV of 15% was regarded as the acceptable upper limit of imprecision. The results obtained by the indirect assays correlated closely with those obtained by corresponding direct sandwich assays. The model assays demonstrated the utility of Eu-labelled streptavidin as a universal reagent for immunoassays requiring a wide dynamic range and high sensitivity.
对用荧光铕离子标记链霉亲和素进行了优化,目的是获得一种通用、稳定且高度灵敏的非同位素标记物,用于基于解离荧光增强(DELFIA)的时间分辨荧光免疫测定 (TR-FIA)。即使将链霉亲和素的所有游离氨基与铕螯合物结合,对该蛋白质的结合能力或其亲和力也只有轻微影响。在人卵泡刺激素和促甲状腺激素(FSH和TSH)的间接时间分辨免疫荧光测定中对标记的链霉亲和素进行了评估。对于FSH样品,在2.5至94 U/l的浓度范围内,批间不精密度低于3%;对于TSH样品,在2.4至35 mIU/l的范围内,批间不精密度低于5%。当将15%的变异系数视为可接受的不精密度上限时,FSH和TSH测定的检测限分别为0.05 - 0.10 U/l和0.01 - 0.025 mIU/l。间接测定获得的结果与相应的直接夹心测定获得的结果密切相关。这些模型测定证明了铕标记的链霉亲和素作为一种通用试剂在需要宽动态范围和高灵敏度的免疫测定中的实用性。