Visualization of molecular binding sites at the nanoscale in the lift-up mode by amplitude-modulation atomic force microscopy
Source abstract
Abstract
We report a new approach to visualize the local distribution of molecular recognition sites with nanoscale resolution by amplitude-modulation atomic force microscopy. By integrating chemical modification of probes, photothermal excitation to drive a cantilever, and lift-up scanning over surface topography, we successfully visualized binding sites provided by streptavidin on a solid surface for biotin attached on an AFM probe. The optimization of measurement conditions was discussed in detail, and the application of the technique was verified with a different ligand-receptor system.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Force Microscopy Techniques and Applications · Molecular Junctions and Nanostructures · Mechanical and Optical Resonators
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tokyo Institute of Technology
Department of Materials Science and Engineering
School of Materials and Chemical Technology
Yokohama
Japan
Funding
Japan Science and Technology Agency · Ministry of Education, Culture, Sports, Science and Technology
References (32)
Show source-provided references
1. Biener · Biol. Cell · 2005 · 97 · 90510.1042/BC20040511 ↗
2. Heiss · J. Nucl. Med. · 2006 · 47 · 302
3. Bonanno · Langmuir · 2007 · 23 · 581710.1021/la063659c ↗
4. Garifullina · Anal. Chem. · 2019 · 91 · 1509010.1021/acs.analchem.9b03780 ↗
5. Chalfie · Science · 1994 · 263 · 80210.1126/science.8303295 ↗
6. Arai · Langmuir · 2011 · 27 · 247810.1021/la104178h ↗
7. Hinterdorfer · Nat. Methods · 2006 · 3 · 34710.1038/nmeth871 ↗
8. Kim · Phys. Chem. Chem. Phys. · 2016 · 18 · 1445410.1039/C6CP01168C ↗
9. Mochizuki · Langmuir · 2015 · 31 · 800610.1021/acs.langmuir.5b01691 ↗
10. Xu · Biophys. J. · 2007 · 93 · 95210.1529/biophysj.106.093229 ↗
11. Dong · Nat. Commun. · 2011 · 2 · 24710.1038/ncomms1246 ↗
12. Efremov · Soft Matter · 2019 · 15 · 545510.1039/C9SM00711C ↗
13. Heath · Nat. Commun. · 2018 · 9 · 498310.1038/s41467-018-07512-3 ↗
14. Kodera · Nature · 2010 · 468 · 7210.1038/nature09450 ↗
15. Carrasco · Rev. Sci. Instrum. · 2008 · 79 · 12610610.1063/1.3053369 ↗
16. Volkov · Appl. Phys. Lett. · 2004 · 85 · 539710.1063/1.1828581 ↗
17. Bar · Langmuir · 1997 · 13 · 380710.1021/la970091m ↗
18. Chen · Ultramicroscopy · 1998 · 75 · 17110.1016/S0304-3991(98)00068-0 ↗
19. Hutter · Rev. Sci. Instrum. · 1993 · 64 · 186810.1063/1.1143970 ↗
20. Proksch · Nanotechnology · 2004 · 15 · 134410.1088/0957-4484/15/9/039 ↗
21. Walters · Rev. Sci. Instrum. · 1996 · 67 · 358310.1063/1.1147177 ↗
22. Kiracofe · Rev. Sci. Instrum. · 2011 · 82 · 01370210.1063/1.3518965 ↗
23. Umeda · J. Vac. Sci. Technol., B · 1991 · 9 · 131810.1116/1.585187 ↗
24. Hayashi · Phys. Chem. Chem. Phys. · 2012 · 14 · 1019610.1039/c2cp41236e ↗
25. Mondarte · RSC Adv. · 2019 · 9 · 2270510.1039/C9RA04106K ↗
26. Tahara · Adv. Mater. Phys. Chem. · 2018 · 08 · 21710.4236/ampc.2018.85014 ↗
27. Caswell · J. Am. Chem. Soc. · 2003 · 125 · 1391410.1021/ja037969i ↗
28. Weber · Science · 1989 · 243 · 8510.1126/science.2911722 ↗
29. Yan · Science · 2003 · 301 · 188210.1126/science.1089389 ↗
30. Chtcheglova · Semin. Cell Dev. Biol. · 2018 · 73 · 4510.1016/j.semcdb.2017.08.025 ↗
31. Olson · Mol. Immunol. · 1989 · 26 · 12910.1016/0161-5890(89)90094-1 ↗
32. Fantner · Ultramicroscopy · 2006 · 106 · 88110.1016/j.ultramic.2006.01.015 ↗