Self-assembled sialyllactosyl probes with aggregation-enhanced properties for ratiometric detection and blocking of influenza viruses
Self-assembled sialyllactosyl probes with aggregation-enhanced properties for ratiometric detection and blocking of influenza viruses作者机构:Key Laboratory for Advanced MaterialsFeringa Nobel Prize Scientist Joint Research CenterSchool of Chernistry and Molecular EngineeringEast China University of Science and TechnologyShanghai 200237China Vaccine Research CenterKey Laboratory of Molecular Virology&ImmunologyInstitut Pasteur of ShanghaiChinese Acadermy of SciencesShanghai 200031China
出 版 物:《Science Bulletin》 (科学通报(英文版))
年 卷 期:2019年第64卷第24期
页 面:1902-1909页
核心收录:
学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学]
基 金:supported by the National Natural Science Foundation of China (21788102,91853201,21722801,21776078) the Shanghai Municipal Science and Technology Major Project (2018SHZDZX03) the National Postdoctoral Program for Innovative Talents (BX20190115)
主 题:Vibration-induced emission Influenza viruses Ratiometric Fluorescence Glycoprobe
摘 要:Infection and dissemination of influenza viruses(IVs) causes serious health concerns ***, effective tools for the accurate detection and blocking of IVs remain elusive. Here, we develop a new sialyllactosyl probe with self-assembled core-shell structure for the ratiometric detection and blocking of IVs. N,N -diaryl-dihydrodibenzo[a,c]phenazines were used to form the core structure by hydrophobic assembly in an aqueous solution with an aggregation-enhanced blue fluorescence ***, dicyanomethylene-4 H-pyran-based sialyllactosides were used for self-assembly with the core structure, producing the sialyllactosyl probe that emits a red fluorescence due to Forster resonance energy transfer. The probe developed has been proven to be available for(1) the fluorescence ratiometric detection of IVs through selective interaction with the sialyllactosyl-binding proteins on the virus surface,and(2) effectively blocking the invasion of human-infecting IVs towards host cells as accentuated by the sialyllactosides on the surface of the probes.