Rajaram Kaushik, Losada-Pérez Patricia, Vermeeren Veronique, Hosseinkhani Baharak, Wagner Patrick, Somers Veerle, Michiels Luc
Biomedical Research Institute (BIOMED), Hasselt University, Hasselt, Belgium.
Institute for Materials Research (IMO), Hasselt University, Diepenbeek, Belgium ; IMEC vzw, Division IMOMEC, Diepenbeek, Belgium.
Int J Nanomedicine. 2015 Aug 19;10:5237-47. doi: 10.2147/IJN.S84800. eCollection 2015.
Over the last three decades, phage display technology has been used for the display of target-specific biomarkers, peptides, antibodies, etc. Phage display-based assays are mostly limited to the phage ELISA, which is notorious for its high background signal and laborious methodology. These problems have been recently overcome by designing a dual-display phage with two different end functionalities, namely, streptavidin (STV)-binding protein at one end and a rheumatoid arthritis-specific autoantigenic target at the other end. Using this dual-display phage, a much higher sensitivity in screening specificities of autoantibodies in complex serum sample has been detected compared to single-display phage system on phage ELISA. Herein, we aimed to develop a novel, rapid, and sensitive dual-display phage to detect autoantibodies presence in serum samples using quartz crystal microbalance with dissipation monitoring as a sensing platform. The vertical functionalization of the phage over the STV-modified surfaces resulted in clear frequency and dissipation shifts revealing a well-defined viscoelastic signature. Screening for autoantibodies using antihuman IgG-modified surfaces and the dual-display phage with STV magnetic bead complexes allowed to isolate the target entities from complex mixtures and to achieve a large response as compared to negative control samples. This novel dual-display strategy can be a potential alternative to the time consuming phage ELISA protocols for the qualitative analysis of serum autoantibodies and can be taken as a departure point to ultimately achieve a point of care diagnostic system.
在过去三十年中,噬菌体展示技术已被用于展示靶标特异性生物标志物、肽、抗体等。基于噬菌体展示的检测方法大多局限于噬菌体酶联免疫吸附测定(ELISA),该方法以其高背景信号和繁琐的方法而臭名昭著。最近,通过设计一种具有两种不同末端功能的双展示噬菌体克服了这些问题,即一端为链霉亲和素(STV)结合蛋白,另一端为类风湿性关节炎特异性自身抗原靶标。与噬菌体ELISA上的单展示噬菌体系统相比,使用这种双展示噬菌体在筛选复杂血清样品中自身抗体的特异性时检测到了更高的灵敏度。在此,我们旨在开发一种新型、快速且灵敏的双展示噬菌体,以使用具有耗散监测功能的石英晶体微天平作为传感平台来检测血清样品中自身抗体的存在。噬菌体在STV修饰表面上的垂直功能化导致了明显的频率和耗散变化,揭示了明确的粘弹性特征。使用抗人IgG修饰的表面和带有STV磁珠复合物的双展示噬菌体筛选自身抗体,能够从复杂混合物中分离出靶标实体,并与阴性对照样品相比获得较大的响应。这种新型双展示策略对于血清自身抗体的定性分析可能是耗时的噬菌体ELISA方案的潜在替代方法,并且可以作为最终实现即时诊断系统的起点。