Comparing Transient Oligonucleotide Hybridization Kinetics Using DNA-PAINT and Optoplasmonic Single-Molecule Sensing on Gold Nanorods

被引:14
|
作者
Eerqing, Narima [1 ,2 ]
Subramanian, Sivaraman [1 ,2 ]
Rubio, Jesus [2 ]
Lutz, Tobias [1 ,2 ]
Wu, Hsin-Yu [1 ,2 ]
Anders, Janet [2 ,3 ]
Soeller, Christian [1 ,2 ]
Vollmer, Frank [1 ,2 ]
机构
[1] Univ Exeter, Living Syst Inst, Exeter EX4 4QD, Devon, England
[2] Univ Exeter, Dept Phys & Astron, Exeter EX4 4QL, Devon, England
[3] Univ Potsdam, Inst Phys & Astron, D-14476 Potsdam, Germany
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
single-molecule; plasmonics; whispering gallery modes; optoplasmonic; DNA-PAINT; fluorescence; localization microscopy; SURFACE-PLASMON RESONANCE; SUPERRESOLUTION MICROSCOPY; LOCALIZATION; RESOLUTION; DEPENDENCE; BIOSENSOR;
D O I
10.1021/acsphotonics.1c01179
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report a comparison of two photonic techniques for single-molecule sensing: fluorescence nanoscopy and optoplasmonic sensing. As the test system, oligonucleotides with and without fluorescent labels are transiently hybridized to complementary "docking" strands attached to gold nanorods. Comparing the measured single-molecule kinetics helps to examine the influence of the fluorescent labels as well as factors arising from different sensing geometries. Our results demonstrate that DNA dissociation is not significantly altered by the fluorescent labels and that DNA association is affected by geometric factors in the two techniques. These findings open the door to exploiting plasmonic sensing and fluorescence nanoscopy in a complementary fashion, which will aid in building more powerful sensors and uncovering the intricate effects that influence the behavior of single molecules.
引用
收藏
页码:2882 / 2888
页数:7
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