Key Laboratory of Nonferrous Metals Chemistry and Resources Utilization of Gansu Province, Lanzhou University, Lanzhou 730000, China; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.
Key Laboratory of Nonferrous Metals Chemistry and Resources Utilization of Gansu Province, Lanzhou University, Lanzhou 730000, China; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.
Talanta. 2015 Jan;131:672-7. doi: 10.1016/j.talanta.2014.08.023. Epub 2014 Aug 19.
Two aptasensors based on graphene oxide (GO) and molecular beacon were designed for the detection of L-tryptophan (L-Trp) using L-Trp aptamer (Trp3a-1). The fluorescein (FAM) labeled Trp3a-1 was absorbed by GO, which resulted in the fluorescence quenching, and exhibiting minimal background fluorescence. Upon the addition of L-Trp, Trp3a-1 was not absorbed quickly. This effect allows for a quantitative assay of L-Trp over the concentration range of 10-500 μM and with a detection limit of 6.84 μM. However, due to the unspecific adsorption of GO, the GO based aptasensor can't be applied in complex matrixes. In respect of molecular beacon based aptasensor, FRET between Trp3a-1 labeled with FAM and CS-Trp3a-1 labeled with BHQ-1(black hole quencher-1) which is partially complementary with the aptamer was used to detect L-Trp. L-Trp binding could induce the disassociation of CS-Trp3a-1, resulted in the enhancement of fluorescence in solution. With an excellent linear relationship in 10-500 μM and a detection limit of 6.97 μM in 25% serum, the aptasensor is expected to be improved for the detection of free L-Trp in other complex samples.
基于石墨烯氧化物 (GO) 和分子信标的两种适体传感器被设计用于使用 L-色氨酸 (L-Trp) 适体 (Trp3a-1) 检测 L-Trp。荧光素 (FAM) 标记的 Trp3a-1 被 GO 吸收,导致荧光猝灭,呈现最小的背景荧光。当加入 L-Trp 时,Trp3a-1 不会被快速吸收。这种效应允许在 10-500 μM 的浓度范围内定量测定 L-Trp,检测限为 6.84 μM。然而,由于 GO 的非特异性吸附,基于 GO 的适体传感器不能应用于复杂基质中。对于基于分子信标的适体传感器,FRET 被用于检测 L-Trp,其原理是 FAM 标记的 Trp3a-1 与 CS-Trp3a-1 之间的相互作用,CS-Trp3a-1 与适体部分互补且被 BHQ-1(黑洞猝灭剂-1)标记。L-Trp 结合可以诱导 CS-Trp3a-1 的解离,导致溶液中荧光增强。在 25%血清中,该适体传感器在 10-500 μM 范围内具有良好的线性关系,检测限为 6.97 μM,有望在其他复杂样品中检测游离 L-Trp 方面得到进一步改进。