Department of Food Science, Cornell University, 241 Stocking Hall, Ithaca, NY, 14853, USA.
Department of Mechanical Engineering, University of California Berkeley, 1113 Etcheverry Hall, Berkeley, CA, 94720, USA.
Anal Bioanal Chem. 2019 May;411(12):2487-2492. doi: 10.1007/s00216-019-01766-6. Epub 2019 Mar 23.
A peptide-graphene oxide nanosensor has been developed to detect tobacco etch virus (TEV) protease and bacteria infected with an engineered bacteriophage. In the detection strategy, a peptide (sequence: RKRFRENLYFQSCP) is tagged with fluorophores and graphene oxide (GO) is used to adsorb the peptides while quenching their fluorescence. In the presence of TEV protease, fluoropeptides are cleaved between glutamine (Q) and serine (S), resulting in the recovery of fluorescence signal. Based on the fluorescent intensity, the detection limit of TEV protease is 51 ng/μL. Additionally, we have utilized the sensing system to detect bacteria cells. Bacteriophages, which were engineered to carry TEV protease genes, were used to infect target bacteria (Escherichia coli) resulting in the translation and release of the protease. This allowed the estimation of bacteria at the concentration of 10 CFU/mL. This strategy has the potential to be developed as a multiplex detection platform of multiple bacterial species. Graphical abstract.
已开发出一种肽-氧化石墨烯纳米传感器,用于检测烟草蚀纹病毒(TEV)蛋白酶和感染工程噬菌体的细菌。在检测策略中,将肽(序列:RKRFRENLYFQSCP)标记上荧光团,并使用氧化石墨烯(GO)吸附肽,同时猝灭其荧光。在 TEV 蛋白酶存在的情况下,荧光肽在谷氨酰胺(Q)和丝氨酸(S)之间被切割,从而恢复荧光信号。基于荧光强度,TEV 蛋白酶的检测限为 51ng/μL。此外,我们还利用传感系统检测细菌细胞。噬菌体被设计携带 TEV 蛋白酶基因,用于感染靶细菌(大肠杆菌),导致蛋白酶的翻译和释放。这使得可以在 10 CFU/mL 的浓度下估计细菌。该策略有可能被开发为多种细菌的多重检测平台。