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Signal on fluorescence biosensor for MMP-2 based on FRET between semiconducting polymer dots and a metal organic framework

机译:半导体聚合物点与金属有机骨架之间基于FRET的MMP-2荧光生物传感器上的信号

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摘要

A signal on fluorescence biosensor for ultrasensitive detection of MMP-2 based on fluorescence resonance energy transfer (FRET) between semiconducting polymer dots (Pdots) and a metal-organic framework (MOF) has been developed. Carboxyl-rich PFO has been modified firmly with a polypeptide chain (COOH-GHHYYGPLGVRGC-NH2) through a carboxy ammonia reaction first. The polypeptide chain comprises the specific MMP-2 substrate domain (PLGVR) and the pi-rich motif (HHYY) can be absorbed by the MOF (H(2)dtoaCu used in this study) through pi-staking interactions. Hence, the fluorescence from Pdots can be quenched by the MOF with the assistance of the polypeptide chain linker through the FRET process. Upon the cleavage of the substrate by the protease (MMP-2) at the amide bond between Gly and Val, the Pdots has been separated from the MOF surface and therefore the FRET process can be inhibited, and the fluorescence of the system recovered. Under optimal conditions, the fluorescence recovery was found to be proportional to the concentration of MMP-2 within the range of 0.1 to 2.5 pg mL(-1).
机译:已经开发了用于基于半导体聚合物点(Pdot)与金属有机骨架(MOF)之间的荧光共振能量转移(FRET)进行MMP-2超灵敏检测的荧光生物传感器信号。富含羧基的PFO已首先通过羧基氨反应用多肽链(COOH-GHHYYGPLGVRGC-NH2)进行了牢固的修饰。多肽链包含特定的MMP-2底物结构域(PLGVR),并且pi富集相互作用可以使MOF(本研究中使用的H(2)dtoaCu)吸收富含pi的基序(HHYY)。因此,在多肽链接头的帮助下,通过FRET过程,MOF可以淬灭来自Pdots的荧光。在Gly和Val之间的酰胺键上被蛋白酶(MMP-2)裂解底物后,Pdots已从MOF表面分离出来,因此可以抑制FRET过程,并恢复系统的荧光。在最佳条件下,发现荧光恢复与MMP-2的浓度在0.1至2.5 pg mL(-1)范围内成正比。

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