State Key Laboratory of Medicinal Chemical Biology, and Department of Chemistry, Nankai University, Tianjin 300071, China; Synergetic Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China.
State Key Laboratory of Medicinal Chemical Biology, and Department of Chemistry, Nankai University, Tianjin 300071, China; Synergetic Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China.
Biosens Bioelectron. 2014 Apr 15;54:266-72. doi: 10.1016/j.bios.2013.11.004. Epub 2013 Nov 12.
A novel epitope molecularly imprinted polymer (EMIP) for specific recognition and direct fluorescent quantification of the target protein bovine serum albumin (BSA) was demonstrated where polymerization was performed on the surface of silica nanospheres embedded CdTe quantum dots (QDs). The synthetic peptide derived from the surface-exposed C-terminus of bovine serum albumin (BSA, residues 599-607) was selected as the template molecule. The resulting EMIP film was able to selectively capture the template peptide and the corresponding target protein BSA via the recognition cavities. Based on the fluorescence quenching, the EMIP-coated QDs (molecular imprinted polymer coating CdTe QDs using epitope as the template) nanospheres were successfully applied to the direct fluorescence quantification of BSA. Compared with BMIP-coated QDs (molecular imprinted polymer coating CdTe QDs using BSA as the template), the imprinting factor and adsorption capacity of EMIP-coated QDs were greatly increased. The prepared EMIP-coated QDs can also discriminate even one mismatched sequences from the original sequences of the epitope of the BSA. The practical analytical performance of the EMIP-coated QDs was examined by evaluating the detection of BSA in the bovine calf serum sample with satisfactory results. In addition, the resulting EMIP-coated QDs nanospheres were also successfully applied to separating BSA from the bovine blood sample.
一种用于特异性识别和直接荧光定量分析目标蛋白牛血清白蛋白(BSA)的新型表位分子印迹聚合物(EMIP)被展示出来,其中聚合反应是在嵌入碲化镉量子点(QDs)的硅纳米球表面上进行的。从牛血清白蛋白(BSA,残基 599-607)表面暴露的 C 末端衍生出的合成肽被选为模板分子。所得的 EMIP 薄膜能够通过识别腔选择性地捕获模板肽和相应的靶蛋白 BSA。基于荧光猝灭,成功地将 EMIP 涂层的 QDs(使用表位作为模板的分子印迹聚合物涂覆 CdTe QDs)纳米球应用于 BSA 的直接荧光定量分析。与 BMIP 涂层的 QDs(使用 BSA 作为模板的分子印迹聚合物涂覆 CdTe QDs)相比,EMIP 涂层的 QDs 的印迹因子和吸附容量大大增加。制备的 EMIP 涂层的 QDs 还可以区分 BSA 表位的原始序列中的一个错配序列。通过评估牛犊血清样品中 BSA 的检测,考察了 EMIP 涂层的 QDs 的实际分析性能,结果令人满意。此外,所得的 EMIP 涂层的 QDs 纳米球还成功地应用于从牛血样中分离 BSA。