Single-Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics

被引:1
|
作者
Zhang, Yiming [1 ,2 ]
Ji, Zongzhou [1 ,3 ]
Wang, Xin [1 ]
Cao, Yi [1 ,4 ,5 ]
Pan, Hai [1 ]
机构
[1] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325001, Peoples R China
[2] Wenzhou Kean Univ, Wenzhou 325060, Peoples R China
[3] Northeastern Univ, Shenyang 110819, Peoples R China
[4] Jinan Microecol Biomed Shandong Lab, Shounuo City Light West Block,Qingdao Rd 3716, Jinan 250117, Peoples R China
[5] Nanjing Univ, Dept Phys, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R China
关键词
single-molecule fluorescence resonance energy transfer; DNAzyme; conformational dynamics; metal ions; IN-VITRO SELECTION; URANYL-ION; FRET; DNA; SENSITIVITY; SENSORS;
D O I
10.3390/ijms24021212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNAzyme is a class of DNA molecules that can perform catalytic functions with high selectivity towards specific metal ions. Due to its potential applications for biosensors and medical therapeutics, DNAzyme has been extensively studied to characterize the relationships between its biochemical properties and functions. Similar to protein enzymes and ribozymes, DNAzymes have been found to undergo conformational changes in a metal-ion-dependent manner for catalysis. Despite the important role the conformation plays in the catalysis process, such structural and dynamic information might not be revealed by conventional approaches. Here, by using the single-molecule fluorescence resonance energy transfer (smFRET) technique, we were able to investigate the detailed conformational dynamics of a uranyl-specific DNAzyme 39E. We observed conformation switches of 39E to a folded state with the addition of Mg2+ and to an extended state with the addition of UO22+. Furthermore, 39E can switch to a more compact configuration with or without divalent metal ions. Our findings reveal that 39E can undergo conformational changes spontaneously between different configurations.
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页数:10
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