Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Brisbane, Qld 4072, Australia.
Biosens Bioelectron. 2012 Oct-Dec;38(1):132-7. doi: 10.1016/j.bios.2012.05.014. Epub 2012 May 30.
An electrochemical immunoassay which minimizes nonspecific protein adsorption and improves detection sensitivity of proteomic cancer biomarker is described. Our technique comprises two novel features: (i) a high density terminally functionalized poly(N-isopropyl acrylamide) 'brush' layer is grown by surface initiated reversible addition fragmentation chain transfer (RAFT) polymerization method from the electrode surface in order to minimize nonspecific adsorption of serum proteins and other biomolecules, and (ii) a signal amplifying 'bionanoconjugate' comprised of graphene oxide nanosheets decorated with CdSe quantum dots and recombinant single-chain variable fragments towards MSLN, is used to 'physically' amplify the anodic stripping voltammetric signal. This method enabled a detection limit of ca. 1 pg/mL MSLN (RSD=4.6%, n=4) spiked in serum samples. Because of the simple, specific and sensitive nature of this methodology, we feel that it may find potential use in serum-based protein diagnostics.
一种电化学免疫分析方法,可最大限度地减少非特异性蛋白质吸附并提高蛋白质组癌症生物标志物的检测灵敏度。我们的技术包括两个新颖的特点:(i)通过表面引发可逆加成-断裂链转移(RAFT)聚合方法从电极表面生长高密度末端官能化的聚(N-异丙基丙烯酰胺)'刷'层,以最大限度地减少血清蛋白和其他生物分子的非特异性吸附,和(ii)信号放大的'生物纳米缀合物'由氧化石墨烯纳米片和重组单链可变片段组成,用于 MSCL,用于'物理'放大阳极溶出伏安信号。该方法使在血清样品中添加的 MSCL 的检测限达到约 1 pg/mL(RSD=4.6%,n=4)。由于这种方法简单、特异性和灵敏性,我们认为它可能在基于血清的蛋白质诊断中具有潜在的用途。