Xi Gaina, Wang Xiaoping, Chen Tongsheng
MOE Key Laboratory of Laser Life Science & College of Biophotonics, South China Normal University, Guangzhou, People's Republic of China.
Department of Pain Management, The First Affiliated Hospital of Jinan University, Guangzhou, People's Republic of China.
Int J Nanomedicine. 2016 Apr 15;11:1537-47. doi: 10.2147/IJN.S102517. eCollection 2016.
A novel fluorescence nanoprobe (reduced nano-graphene oxide [nrGO]/fluorescein isothiocyanate-labeled peptide [Pep-FITC]) for ultrasensitive detection of matrix metalloproteinase 2 (MMP2) has been developed by engineering the Pep-FITC comprising the specific MMP2 substrate domain (PLGVR) onto the surface of nrGO particles through non-covalent linkage. The nrGO was obtained by water bathing nano-graphene oxide under 90°C for 4 hours. After mixing the nrGO and Pep-FITC for 30 seconds, the fluorescence from Pep-FITC was almost completely quenched due to the fluorescence resonance energy transfer between fluorescein isothiocyanate (FITC) and nrGO. Upon cleavage of the amide bond between Leu and Gly in the Pep-FITC by protease-MMP2, the FITC bound to nrGO was separated from nrGO surface, disrupting the fluorescence resonance energy transfer process and resulting in fluorescence recovery of FITC. Under optimal conditions, the fluorescence recovery of nrGO/Pep-FITC was found to be directly proportional to the concentration of MMP2 within 0.02-0.1 nM. The detection limit of the nrGO/Pep-FITC was determined to be 3 pM, which is approximately tenfold lower than that of the unreduced carboxylated nano-graphene oxide/Pep-FITC probe.
一种用于超灵敏检测基质金属蛋白酶2(MMP2)的新型荧光纳米探针(还原型氧化石墨烯[nrGO]/异硫氰酸荧光素标记肽[Pep-FITC])已通过将包含特定MMP2底物结构域(PLGVR)的Pep-FITC通过非共价连接工程化到nrGO颗粒表面而开发出来。nrGO是通过在90°C下水浴氧化石墨烯4小时获得的。将nrGO和Pep-FITC混合30秒后,由于异硫氰酸荧光素(FITC)和nrGO之间的荧光共振能量转移,Pep-FITC的荧光几乎完全猝灭。当蛋白酶-MMP2切割Pep-FITC中Leu和Gly之间的酰胺键时,与nrGO结合的FITC从nrGO表面分离,破坏了荧光共振能量转移过程,导致FITC荧光恢复。在最佳条件下,发现nrGO/Pep-FITC的荧光恢复与0.02-0.1 nM范围内的MMP2浓度成正比。nrGO/Pep-FITC的检测限确定为3 pM,比未还原的羧基化氧化石墨烯/Pep-FITC探针低约十倍。