Rao Ashwin K, Creager Stephen E
Advanced Material Research Laboratories, 91 Technology Drive, Anderson, SC 29625, USA.
Anal Chim Acta. 2008 Nov 3;628(2):190-7. doi: 10.1016/j.aca.2008.09.019. Epub 2008 Sep 12.
We report on the use of flow-through electrodes fabricated from a composite of superporous agarose (SPA) and reticulated vitreous carbon (RVC) for carrying out sandwich bioassays via a model sandwich assay scheme. The flow-through design of the SPA-RVC electrodes allows for ease in solution handling with the use of micropipettors while allowing sandwich assays to be performed on the SPA matrix inside the RVC. A sandwich bioassay was devised for detecting biotinylated bovine serum albumin (b-BSA) as a proof-of-concept scheme to demonstrate applicability of SPA-RVC electrodes to carry out sandwich assays. In this bioassay scheme, SPA-RVC electrodes with avidin molecules immobilized on the SPA matrix were incubated with low quantities of b-BSA followed by incubation with avidinylated alkaline phosphatase (av-ALP). This construct creates a sandwich bioassay whereby b-BSA is sandwiched between the two avidin complexes. Av-ALP labels captured on the bound b-BSA catalytically hydrolyze conversion of 4-aminophenylphosphate (PAPP) to electrochemically active 4-aminophenol (PAP) which is then voltammetrically detected inside the RVC. The lower concentration detection limit for b-BSA was 0.32+/-0.1 ng mL(-1) and the absolute detection limit was 32+/-10 pg. Non-specific binding of av-ALP enzyme labels onto the avidin-activated SPA-RVC electrodes was low. Catalytic generation of PAP by non-specifically bound av-ALP occurs at a rate less than 2% of that for PAP generation by av-ALP in [(SPA-av)-(b-BSA-b)-(av-ALP)] sandwich constructs.
我们报告了使用由超多孔琼脂糖(SPA)和网状玻璃碳(RVC)复合材料制成的流通电极,通过模型夹心分析方案进行夹心生物测定。SPA-RVC电极的流通设计便于使用微量移液器处理溶液,同时允许在RVC内部的SPA基质上进行夹心分析。设计了一种用于检测生物素化牛血清白蛋白(b-BSA)的夹心生物测定法,作为概念验证方案,以证明SPA-RVC电极进行夹心分析的适用性。在该生物测定方案中,将固定有抗生物素蛋白分子的SPA-RVC电极与少量b-BSA孵育,然后与抗生物素蛋白化碱性磷酸酶(av-ALP)孵育。这种构建物形成了一种夹心生物测定法,其中b-BSA夹在两种抗生物素蛋白复合物之间。捕获在结合的b-BSA上的av-ALP标签催化4-氨基苯磷酸酯(PAPP)转化为具有电化学活性的4-氨基苯酚(PAP),然后在RVC内部通过伏安法进行检测。b-BSA的较低浓度检测限为0.32±0.1 ng mL(-1),绝对检测限为32±10 pg。av-ALP酶标签在抗生物素蛋白激活的SPA-RVC电极上的非特异性结合较低。非特异性结合的av-ALP催化生成PAP的速率低于[(SPA-av)-(b-BSA-b)-(av-ALP)]夹心构建物中av-ALP生成PAP速率的2%。