Graphene-on-Glass Preparation and Cleaning Methods Characterized by Single-Molecule DNA Origami Fluorescent Probes and Raman Spectroscopy

被引:25
作者
Krause, Stefan [1 ,2 ]
Ploetz, Evelyn [1 ,2 ]
Bohlen, Johann [1 ,2 ]
Schuler, Patrick [1 ,2 ]
Yaadav, Renukka [1 ,2 ]
Selbach, Florian [1 ,2 ]
Steiner, Florian [1 ,2 ]
Kaminska, Izabela [3 ]
Tinnefeld, Philip [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Chem, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Ctr NanoSci CeNS, D-81377 Munich, Germany
[3] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
关键词
graphene; DNA origami; Raman spectroscopy; fluorescence quenching; single-molecule spectroscopy; fluorescence lifetime imaging microscopy; INDUCED ENERGY-TRANSFER; FILMS; OXIDE;
D O I
10.1021/acsnano.0c08383
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene exhibits outstanding fluorescence quenching properties that can become useful for biophysics and biosensing applications, but it remains challenging to harness these advantages due to the complex transfer procedure of chemical vapor deposition-grown graphene to glass coverslips and the low yield of usable samples. Here, we screen 10 graphene-on-glass preparation methods and present an optimized protocol. To obtain the required quality for single-molecule and super-resolution imaging on graphene, we introduce a graphene screening method that avoids consuming the investigated sample. We apply DNA origami nanostructures to place fluorescent probes at a defined distance on top of graphene-on-glass coverslips. Subsequent fluorescence lifetime imaging directly reports on the graphene quality, as deviations from the expected fluorescence lifetime indicate imperfections. We compare the DNA origami probes with conventional techniques for graphene characterization, including light microscopy, atomic force microscopy, and Raman spectroscopy. For the latter, we observe a discrepancy between the graphene quality implied by Raman spectra in comparison to the quality probed by fluorescence lifetime quenching measured at the same position. We attribute this discrepancy to the difference in the effective area that is probed by Raman spectroscopy and fluorescence quenching. Moreover, we demonstrate the applicability of already screened and positively evaluated graphene for studying single-molecule conformational dynamics on a second DNA origami structure. Our results constitute the basis for graphene-based biophysics and super-resolution microscopy.
引用
收藏
页码:6430 / 6438
页数:9
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