Li Chenghui, Wu Peng, Hou Xiandeng
Key Lab of Green Chemistry and Technology of Ministry of Education, College of Chemistry, and Analytical & Testing Center, Sichuan University, Chengdu 610064, China.
Nanoscale. 2016 Feb 21;8(7):4291-8. doi: 10.1039/c5nr09130f.
Information extraction from nano-bio-systems is crucial for understanding their inner molecular level interactions and can help in the development of multidimensional/multimodal sensing devices to realize novel or expanded functionalities. The intrinsic fluorescence (IF) of proteins has long been considered as an effective tool for studying protein structures and dynamics, but not for protein recognition analysis partially because it generally contributes to the fluorescence background in bioanalysis. Here we explored the use of IF as the fourth channel optical input for a multidimensional optosensing device, together with the triple-channel optical output of Mn-doped ZnS QDs (fluorescence from ZnS host, phosphorescence from Mn(2+) dopant, and Rayleigh light scattering from the QDs), to dramatically improve the protein recognition and discrimination resolution. To further increase the cross-reactivity of the multidimensional optosensing device, plasma modification of proteins was explored to enhance the IF difference as well as their interactions with Mn-doped ZnS QDs. Such a sensor device was demonstrated for highly discriminative and precise identification of proteins in human serum and urine samples, and for cancer and normal cells as well.
从纳米生物系统中提取信息对于理解其内部分子水平的相互作用至关重要,并且有助于开发多维/多模态传感设备以实现新颖或扩展的功能。蛋白质的固有荧光(IF)长期以来一直被视为研究蛋白质结构和动力学的有效工具,但不适用于蛋白质识别分析,部分原因是它通常会在生物分析中形成荧光背景。在此,我们探索将IF用作多维光传感设备的第四通道光学输入,与掺锰硫化锌量子点的三通道光学输出(硫化锌主体的荧光、锰(2+)掺杂剂的磷光以及量子点的瑞利光散射)相结合,以显著提高蛋白质识别和区分分辨率。为了进一步提高多维光传感设备的交叉反应性,研究了对蛋白质进行等离子体修饰,以增强IF差异以及它们与掺锰硫化锌量子点的相互作用。这种传感设备被证明可用于高度区分和精确识别血清和尿液样本中的蛋白质,以及癌细胞和正常细胞。