Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, and DAILAB, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8566, Japan.
Faculty of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8573, Japan.
Sensors (Basel). 2017 Sep 23;17(10):2194. doi: 10.3390/s17102194.
Signature-based protein sensing has recently emerged as a promising prospective alternative to conventional lock-and-key methods. However, most of the current examples require the measurement of optical signals from spatially-separated materials for the generation of signatures. Herein, we present a new approach for the construction of multi-fluorescent sensing systems with high accessibility and tunability, which allows generating protein fluorescent signatures from a single microplate well. This approach is based on conjugates between nano-graphene oxide (nGO) and three single-stranded DNAs (ssDNAs) that exhibit different sequences and fluorophores. Initially, the three fluorophore-modified ssDNAs were quenched simultaneously by binding to nGO. Subsequent addition of analyte proteins caused a partial recovery in fluorescent intensity of the individual ssDNAs. Based on this scheme, we have succeeded in acquiring fluorescence signatures unique to (i) ten proteins that differ with respect to pI and molecular weight and (ii) biochemical marker proteins in the presence of interferent human serum. Pattern-recognition methods demonstrated high levels of discrimination for this system. The high discriminatory power and simple format of this sensor system should enable an easy and fast evaluation of proteins and protein mixtures.
基于特征的蛋白质传感技术最近作为一种有前途的替代传统锁钥方法而出现。然而,目前大多数的例子都需要从空间分离的材料中测量光学信号,以产生特征。在此,我们提出了一种新的方法来构建具有高可及性和可调性的多荧光传感系统,该系统允许从单个微孔板孔中生成蛋白质荧光特征。这种方法基于纳米氧化石墨烯(nGO)和三种具有不同序列和荧光团的单链 DNA(ssDNA)之间的缀合物。最初,三种荧光团修饰的 ssDNA 通过与 nGO 结合而被同时猝灭。随后加入分析物蛋白质会导致个别 ssDNA 的荧光强度部分恢复。基于该方案,我们成功地获得了( i )十个在等电点和分子量方面不同的蛋白质和( ii )在存在干扰人血清的情况下的生化标记蛋白的独特荧光特征。模式识别方法证明了该系统具有很高的区分能力。这种传感器系统的高区分能力和简单的格式应该能够实现对蛋白质和蛋白质混合物的快速评估。