Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT, USA.
ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT, USA.
J Appl Lab Med. 2022 May 4;7(3):762-775. doi: 10.1093/jalm/jfab169.
Streptavidin-to-biotin binding is one of the strongest noncovalent interactions in nature and incorporated into many immunoassays. Biotin-streptavidin coupling assays are susceptible to interference from free biotin in patient specimens, which may falsely decrease or increase results. To prevent biotin interference, we evaluated a method to preconjugate biotinylated antibodies to the assay's streptavidin solid surface before adding patient specimen and compared this technique to a biotin depletion protocol.
Biotin interference in 3 manual ELISAs and 2 automated immunoassays was established. Mitigation of biotin interference by preincubation was evaluated in each assay by adding biotinylated antibody to the streptavidin-coated surface before adding biotin- or PBS-spiked serum. Lastly, the preincubation method was compared to a biotin-depletion protocol to compare the effectiveness of mitigating biotin interference.
In the presence of 400 µg/L biotin, analyte detection was reduced to 10% to 15% of total in the ELISA assays and to 15.2% in the automated sandwich (thyroglobulin) immunoassay. In the automated competitive (free thyroxine) immunoassay, biotin caused an increased detection of 551.6%. Preconjugation of the biotinylated capture antibody to the streptavidin surface in the ELISA assays resulted in 84% to 99% activity recovery, compared to 84% to 97% by a biotin depletion protocol. Similarly, automated sandwich and competitive immunoassays obtained 97.1% and 116.5% recovery by preconjugation, compared to 95.6% and 100.3% by the depletion method, respectively.
This study demonstrates how assay redesign to include preconjugation of biotinylated capture antibody to streptavidin is an effective alternative to biotin-depletion methods to mitigate biotin interference.
链霉亲和素与生物素的结合是自然界中最强的非共价相互作用之一,并被应用于许多免疫测定中。生物素-链霉亲和素偶联测定法容易受到患者标本中游离生物素的干扰,这可能会导致结果假性降低或升高。为了防止生物素干扰,我们评估了一种方法,即在加入患者标本之前,将生物素化抗体预先偶联到测定法的链霉亲和素固相表面上,并将该技术与生物素耗尽方案进行了比较。
在 3 种手动 ELISA 和 2 种自动免疫测定中建立了生物素干扰。通过在加入生物素或 PBS 加标血清之前,将生物素化抗体加入到链霉亲和素包被的表面上,评估了在每种测定中预孵育对生物素干扰的缓解作用。最后,将预孵育方法与生物素耗尽方案进行了比较,以比较缓解生物素干扰的效果。
在存在 400μg/L 生物素的情况下,分析物的检测降低到 ELISA 测定法中总检测值的 10%至 15%,在自动夹心(甲状腺球蛋白)免疫测定法中降低到 15.2%。在自动竞争(游离甲状腺素)免疫测定中,生物素导致检测值增加了 551.6%。将生物素化捕获抗体预先偶联到 ELISA 测定法中的链霉亲和素表面上,与生物素耗尽方案相比,可获得 84%至 99%的活性回收率,分别为 84%至 97%。同样,自动夹心和竞争免疫测定法通过预偶联获得 97.1%和 116.5%的回收率,而通过耗尽方法分别获得 95.6%和 100.3%的回收率。
本研究表明,如何重新设计测定法以包括将生物素化捕获抗体预先偶联到链霉亲和素上,是一种有效替代生物素耗尽方法的方法,可用于缓解生物素干扰。