Biomicrofluidics. 2012 Jun;6(2):24126-2412612. doi: 10.1063/1.4722588. Epub 2012 May 24.
Determination of amyloid β (Aβ) isoforms and in particular the proportion of the Aβ 1-42 isoform in cerebrospinal fluid (CSF) of patients suspected of Alzheimer's disease might help in early diagnosis and treatment of that illness. Due to the low concentration of Aβ peptides in biological fluids, a preconcentration step prior to the detection step is often necessary. This study utilized on-chip immunoprecipitation, known as micro-immunoprecipitation (μIP). The technique uses an immunosorbent (IS) consisting of magnetic beads coated with specific anti-Aβ antibodies organized into an affinity microcolumn by a magnetic field. Our goal was to thoroughly describe the critical steps in developing the IS, such as selecting the proper beads and anti-Aβ antibodies, as well as optimizing the immobilization technique and μIP protocol. The latter includes selecting optimal elution conditions. Furthermore, we demonstrate the efficiency of anti-Aβ IS for μIP and specific capture of 5 Aβ peptides under optimized conditions using various subsequent analytical methods, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), capillary electrophoresis, microchip electrophoresis, and immunoblotting. Synthetic Aβ peptides samples prepared in buffer and spiked in human CSF were analyzed. Finally, on-chip immunoprecipitation of Aβ peptides in human CSF sample was performed.
测定疑似阿尔茨海默病患者脑脊液(CSF)中的淀粉样蛋白β(Aβ)异构体,特别是 Aβ1-42 异构体的比例,可能有助于该病的早期诊断和治疗。由于 Aβ 肽在生物体液中的浓度较低,因此在检测步骤之前通常需要进行预浓缩步骤。本研究利用了芯片上免疫沉淀,即微免疫沉淀(μIP)。该技术使用一种免疫吸附剂(IS),由涂有特定抗 Aβ 抗体的磁性珠组成,通过磁场将其组织成亲和微柱。我们的目标是彻底描述开发 IS 的关键步骤,例如选择合适的珠子和抗 Aβ 抗体,以及优化固定化技术和 μIP 方案。后者包括选择最佳的洗脱条件。此外,我们展示了抗 Aβ IS 用于 μIP 的效率以及在优化条件下使用各种后续分析方法(包括基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)、毛细管电泳、微芯片电泳和免疫印迹)对 5 种 Aβ 肽的特异性捕获。在缓冲液中制备并掺入人 CSF 的合成 Aβ 肽样品进行了分析。最后,在人 CSF 样品上进行了芯片上 Aβ 肽的免疫沉淀。