journal article·2025

An oxygen-scavenging system without impact on DNA mechanical properties in single-molecule fluorescence experiments

Shang Gao, Jialun Liang, Chuang Tan, Jie Ma

Nanoscale· Volume 17· Issue 6
Publisher page

Abstract

Oxygen scavenging systems (OSSs) are critical for dye stability in single-molecule fluorescence (SMF) experiments. However, the commonly used protocatechuic acid (PCA)/protocatechuate-3,4-dioxygenase (PCD) OSS alters DNA mechanical properties, limiting its applicability. To address this limitation, we examine the bilirubin oxidase (BOD) OSS, which had not been previously used in single-molecule experiments, alongside the pyranose oxidase and catalase (POC) OSS. Our results revealed that POC OSS affected DNA mechanics in a buffer-dependent manner, while BOD OSS had no discernible effect across all tested buffer conditions. Furthermore, BOD OSS significantly extended the photobleaching lifetimes of Cy3 and Cy5 dyes and caused minimal pH changes compared to PCD OSS. Collectively, these findings highlight the superior performance of BOD OSS, suggesting its potential for widespread application, particularly in experiments combining SMF with single-molecule force spectroscopy (SMFS) measurements.
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Research context

OpenAlex topics: Advanced Fluorescence Microscopy Techniques · Advanced biosensing and bioanalysis techniques · DNA and Nucleic Acid Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Physics, Sun Yat-sen University, Guangzhou 510275, People's Republic of China

State Key Laboratory of Optoelectronic Materials and Technologies, Sun Yat-sen University, Guangzhou 510006, China

Funding

National Natural Science Foundation of China

References (36)

Show source-provided references
1. Zhuang · Curr. Opin. Struct. Biol. · 2003 · 13 · 8810.1016/S0959-440X(03)00011-3 ↗
2. Schuler · ChemPhysChem · 2005 · 6 · 120610.1002/cphc.200400609 ↗
3. Min · Acc. Chem. Res. · 2005 · 38 · 92310.1021/ar040133f ↗
4. Lu · Adv. Virus Res. · 2019 · 105 · 23910.1016/bs.aivir.2019.07.004 ↗
5. Basu · Nature · 2021 · 589 · 46210.1038/s41586-020-03052-3 ↗
6. Zheng · Chem. Soc. Rev. · 2014 · 43 · 104410.1039/C3CS60237K ↗
7. Roy · Nat. Methods · 2008 · 5 · 50710.1038/nmeth.1208 ↗
8. Lerner · eLife · 2021 · 10 · e6041610.7554/eLife.60416 ↗
9. Aitken · Biophys. J. · 2008 · 94 · 182610.1529/biophysj.107.117689 ↗
10. Swoboda · ACS Nano · 2012 · 6 · 636410.1021/nn301895c ↗
11. Senavirathne · Nat. Methods · 2015 · 12 · 90110.1038/nmeth.3588 ↗
12. Senavirathne · Anal. Biochem. · 2018 · 556 · 7810.1016/j.ab.2018.06.016 ↗
13. Chua · Annu. Rev. Biophys. · 2024 · 53 · 16910.1146/annurev-biophys-030822-032904 ↗
14. Klaue · Nat. Commun. · 2013 · 4 · 202410.1038/ncomms3024 ↗
15. Kemmerich · Nano Lett. · 2016 · 16 · 38110.1021/acs.nanolett.5b03956 ↗
16. Grashoff · Nature · 2010 · 466 · 26310.1038/nature09198 ↗
17. Lee · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · 498510.1073/pnas.0911528107 ↗
18. Naqvi · Nat. Chem. Biol. · 2022 · 18 · 101410.1038/s41589-022-01082-8 ↗
19. Mitra · Nat. Commun. · 2019 · 10 · 431810.1038/s41467-019-12299-y ↗
20. M. M.Soniat , L. R.Myler and J. M.Schaub , et al. , in Methods in Enzymology , ed. B. F. Eichman , Academic Press , 2017 , vol. 592 , pp. 259–281
21. Hu · Nanoscale · 2018 · 10 · 661110.1039/C7NR08397A ↗
22. Kim · Nat. Commun. · 2015 · 6 · 699210.1038/ncomms7992 ↗
23. Marko · Macromolecules · 1995 · 28 · 875910.1021/ma00130a008 ↗
24. Tapia-Rojo · Proc. Natl. Acad. Sci. U. S. A. · 2019 · 116 · 787310.1073/pnas.1821284116 ↗
25. Liu · Chem. Phys. Lett. · 2017 · 678 · 3510.1016/j.cplett.2017.04.028 ↗
26. Biebricher · Nat. Commun. · 2015 · 6 · 730410.1038/ncomms8304 ↗
27. J.Ma , C.Tan and M. D.Wang , in Molecular Motors: Methods and Protocols , ed. C. Lavelle , Springer New York , New York, NY , 2018 , pp. 301–33210.1007/978-1-4939-8556-2_16 ↗
28. Ma · Acta Phys. Sin. · 2018 · 67 · 14870210.7498/aps.67.20180441 ↗
29. Morfill · Biophys. J. · 2007 · 93 · 240010.1529/biophysj.107.106112 ↗
30. Lipfert · Nucleic Acids Res. · 2010 · 38 · 712210.1093/nar/gkq598 ↗
31. Hohng · Science · 2007 · 318 · 27910.1126/science.1146113 ↗
32. Monteiro · Biosens. Bioelectron. · 2022 · 217 · 11472010.1016/j.bios.2022.114720 ↗
33. Bouchiat · Biophys. J. · 1999 · 76 · 40910.1016/S0006-3495(99)77207-3 ↗
34. Wang · Biophys. J. · 1997 · 72 · 133510.1016/S0006-3495(97)78780-0 ↗
35. Edelstein · J. Microbiol. Methods · 2014 · 1 · e10
36. Preus · Nat. Methods · 2015 · 12 · 59310.1038/nmeth.3435 ↗