School of Science, Harbin Institute of Technology, Shenzhen 518055, China.
Department of Nephrology, Shenzhen Hengsheng Hospital, Shenzhen 518102, China.
Anal Chem. 2024 May 14;96(19):7602-7608. doi: 10.1021/acs.analchem.4c00501. Epub 2024 Apr 26.
Molecular imprinting techniques have attracted a lot of attention as a potential biomimetic technology, but there are still challenges in protein imprinting. Herein, multifunctional nanosized molecularly imprinted polymers (nanoMIPs) for human angiotensin-converting enzyme 2 (ACE2) were prepared by epitope imprinting of magnetic nanoparticles-anchored peptide (magNP-P) templates, which were further applied to construct a competitive displacement fluorescence assay toward ACE2. A cysteine-flanked dodecapeptide sequence was elaborately selected as an epitope for ACE2, which was immobilized onto the surface of magnetic nanoparticles and served as a magNP-P template for imprinting. During polymerization, fluorescent monomers were introduced to endow fluorescence responsiveness to the prepared self-signaling nanoMIPs. A competitive displacement fluorescence assay based on the nanoMIPs was established and operated in a washing-free manner, yielding a wide range for ACE2 (0.1-6.0 pg/mL) and a low detection limit (0.081 pg/mL). This approach offers a promising avenue in the preparation of nanoMIPs for macromolecule recognition and expands potential application of an MIP in the detection of proteins as well as peptides.
分子印迹技术作为一种潜在的仿生技术引起了广泛关注,但在蛋白质印迹方面仍存在挑战。在此,通过磁性纳米粒子锚定肽(magNP-P)模板的表位印迹,制备了用于人血管紧张素转换酶 2(ACE2)的多功能纳米尺寸分子印迹聚合物(nanoMIPs),并进一步应用于构建 ACE2 的竞争性荧光检测。精心选择了一个带有半胱氨酸的十二肽序列作为 ACE2 的表位,该序列固定在磁性纳米粒子的表面上,并作为印迹的 magNP-P 模板。在聚合过程中,引入荧光单体赋予制备的自信号 nanoMIPs 荧光响应性。建立了基于 nanoMIPs 的竞争性荧光检测,无需洗涤即可操作,ACE2 的检测范围很宽(0.1-6.0 pg/mL),检测限低(0.081 pg/mL)。该方法为用于大分子识别的 nanoMIPs 的制备提供了一种有前途的途径,并扩展了 MIP 在蛋白质和肽检测中的潜在应用。