材料科学                        
                
                                
                        
                            纳米技术                        
                
                                
                        
                            纵向                        
                
                                
                        
                            肽                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            生物                        
                
                                
                        
                            艺术史                        
                
                                
                        
                            艺术                        
                
                        
                    
            作者
            
                Yuanyuan Zhao,Xu Zhang,Zhipeng Li,Shuaidong Huo,Ke Zhang,Juntao Gao,Hao Wang,Xing‐Jie Liang            
         
                    
        
    
            
            标识
            
                                    DOI:10.1002/adma.201601128
                                    
                                
                                 
         
        
                
            摘要
            
            Simultaneous precise localization and activity evaluation of a biomolecule in a single living cell is through an enzyme‐specific signal‐amplification process, which involves the localized, site‐specific self‐assembly, and activation of a presignaling molecule. The inactive presignaling tetraphenylethylene (TPE)‐peptide derivative, TPE‐YpYY, is nondetectable and highly biocompatible and these small molecules rapidly diffuse into living cells. Upon safely arriving at an active site, and accessing the catalytic pocket of an enzyme, TPE‐YpYY immediately and quantitatively accumulates in situ in response to enzymatic activity, forms an enzyme anchor TPE‐YYY nanoassembly, displays aggregation‐induced emission behavior, and finally lights up the active enzyme, indicating its activity, and allowing its status in living cells to be tracked. This simple and direct self‐portrait method can be used to monitor dynamic self‐assembly processes in individual living cells and may provide new insights that reveal undiscovered biological processes and that aid in developing biomedical hybrid devices. In the future, this strategy of molecular design can be further expanded to the noninvasive investigation of other bioactive molecules, thus facilitating quantitative imaging.
         
            
 
                 
                
                    
                    科研通智能强力驱动
Strongly Powered by AbleSci AI