Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan.
Sci Rep. 2017 Aug 1;7(1):7053. doi: 10.1038/s41598-017-07571-4.
Fluorous-modified surfaces have emerged as a powerful tool for the immobilization of fluorous-tagged biomolecules based on their specificity and the strength of fluorous-fluorous interactions. To fabricate a fluorous-based protein microarray, we designed two strategies for site-specific modification of proteins with a fluorous tag: attaching the fluorous tag to the C-termini of expressed proteins by native chemical ligation (NCL) or to the Fc domain of antibodies through boronic acid (BA)-diol interactions. The perfluoro-tagged proteins could be easily purified by fluorous-functionalized magnetic nanoparticles (MNPs) and immobilized on a fluorous chip with minimal non-specific adsorption. Importantly, proteins immobilized on the solid support through non-covalent fluorous-fluorous interactions were sufficiently stable to withstand continuous washing. We believe that this fluorous-fluorous immobilization strategy will be a highly valuable tool in protein microarray fabrication.
氟修饰表面已成为固定氟标记生物分子的有力工具,这基于其特异性和氟-氟相互作用的强度。为了制备基于氟的蛋白质微阵列,我们设计了两种策略用于蛋白质的定点氟标记:通过天然化学连接(NCL)将氟标记物连接到表达蛋白的 C 末端,或通过硼酸(BA)-二醇相互作用将氟标记物连接到抗体的 Fc 结构域。全氟标记的蛋白质可以通过氟功能化磁性纳米颗粒(MNPs)轻松纯化,并通过最小的非特异性吸附固定在氟芯片上。重要的是,通过非共价氟-氟相互作用固定在固体支持物上的蛋白质足够稳定,可以承受连续洗涤。我们相信,这种氟-氟固定化策略将成为蛋白质微阵列制备的一种非常有价值的工具。