Anal Chem. 2018 Mar 6;90(5):3024-3029. doi: 10.1021/acs.analchem.7b05341. Epub 2018 Feb 22.
Upconversion nanoparticles (UCNPs) are new optical probes for biological applications. For specific biomolecular recognition to be realized for diagnosis and imaging, the key lies in developing a stable and easy-to-use bioconjugation method for antibody modification. Current methods are not yet satisfactory regarding conjugation time, stability, and binding efficiency. Here, we report a facile and high-yield approach based on a bispecific antibody (BsAb) free of chemical reaction steps. One end of the BsAb is designed to recognize methoxy polyethylene glycol-coated UCNPs, and the other end of the BsAb is designed to recognize the cancer antigen biomarker. Through simple vortexing, BsAb-UCNP nanoprobes form within 30 min and show higher (up to 54%) association to the target than that of the traditional UCNP nanoprobes in the ELISA-like assay. We further demonstrate its successful binding to the cancer cells with high efficiency and specificity for background-free fluorescence imaging under near-infrared excitation. This method suggests a general approach broadly suitable for functionalizing a range of nanoparticles to specifically target biomolecules.
上转换纳米粒子(UCNPs)是用于生物应用的新型光学探针。为了实现特定的生物分子识别以进行诊断和成像,关键在于开发用于抗体修饰的稳定且易于使用的生物偶联方法。目前的方法在偶联时间、稳定性和结合效率方面还不尽如人意。在这里,我们报告了一种基于无化学反应步骤的双特异性抗体(BsAb)的简便、高产的方法。BsAb 的一端设计用于识别甲氧基聚乙二醇包覆的 UCNPs,而 BsAb 的另一端设计用于识别癌症抗原生物标志物。通过简单的涡旋,BsAb-UCNP 纳米探针在 30 分钟内形成,并且在 ELISA 样测定中与目标的结合率(高达 54%)高于传统的 UCNP 纳米探针。我们进一步证明了它在近红外激发下对癌细胞的高效和特异性结合,实现了无背景荧光成像。该方法为功能化一系列纳米颗粒以特异性靶向生物分子提供了一种普遍适用的方法。