TY - JOUR
T1 - Single-molecule dynamic structural biology with vertically arranged DNA on a fluorescence microscope
AU - Szalai, Alan M.
AU - Ferrari, Giovanni
AU - Richter, Lars
AU - Hartmann, Jakob
AU - Kesici, Merve Zeynep
AU - Ji, Bosong
AU - Coshic, Kush
AU - Dagleish, Martin R.J.
AU - Jaeger, Annika
AU - Aksimentiev, Aleksei
AU - Tessmer, Ingrid
AU - Kamińska, Izabela
AU - Vera, Andrés M.
AU - Tinnefeld, Philip
N1 - We thank the members of the Tinnefeld group for discussions and feedback. L.R. acknowledges S. Krause who suggested preliminary experiments leading to the discovery of GETvNA. Furthermore, we thank P. Sch\u00FCler, T. Schr\u00F6der and J. Z\u00E4hringer for fruitful discussions. P.T. and I.K. thank, for financial support by the Deutsche Forschungsgemeinschaft (DFG; German Research Foundation) under grant numbers TI 329/14-1 and KA 5449/2-1, the excellence cluster e-conversion under Germany\u2019s Excellence Strategy \u2013 EXC 2089/1 \u2013 390776260, and by the Center for NanoScience (CeNS). P.T thanks funding by the Federal Ministry of Education and Research (BMBF, 13N16929) and the Free State of Bavaria under the Excellence Strategy of the Federal Government and the L\u00E4nder through the ONE MUNICH Project Munich Multiscale Biofabrication. L.R. acknowledges support by the Studienstiftung des deutschen Volkes. A.M.S. is thankful for the support by the Alexander von Humboldt foundation under reference Ref 3.2-ARG-1220722-GF-P. I.K. acknowledges support by the National Science Center of Poland (Sonata 2019/35/D/ST5/00958). K.C. and A.A. were supported by the US National Science Foundation (DMR-1827346) and the Human Frontier Science Program (RGP0047/2020). The supercomputer time was provided through ACESSS allocation grant MCA05S028 (A.A.) and the Leadership Resource Allocation MCB20012 on Frontera of the Texas Advanced Computing Centre (A.A). I.T. acknowledges financial support by the Deutsche Forschungsgemeinschaft (DFG; German Research Foundation), under grant number TE671/7-1. A.M.V. acknowledges financial support by the Deutsche Forschungsgemeinschaft (DFG; German Research Foundation) under project number 522200875.
PY - 2025/1
Y1 - 2025/1
N2 - The intricate interplay between DNA and proteins is key for biological functions such as DNA replication, transcription and repair. Dynamic nanoscale observations of DNA structural features are necessary for understanding these interactions. Here we introduce graphene energy transfer with vertical nucleic acids (GETvNA), a method to investigate DNA–protein interactions that exploits the vertical orientation adopted by double-stranded DNA on graphene. This approach enables the dynamic study of DNA conformational changes via energy transfer from a probe dye to graphene, achieving spatial resolution down to the Ångström scale at subsecond temporal resolution. We measured DNA bending induced by adenine tracts, bulges, abasic sites and the binding of endonuclease IV. In addition, we observed the translocation of the O6-alkylguanine DNA alkyltransferase on DNA, reaching single base-pair resolution and detecting preferential binding to adenine tracts. This method promises widespread use for dynamical studies of nucleic acids and nucleic acid–protein interactions with resolution so far reserved for traditional structural biology techniques.
AB - The intricate interplay between DNA and proteins is key for biological functions such as DNA replication, transcription and repair. Dynamic nanoscale observations of DNA structural features are necessary for understanding these interactions. Here we introduce graphene energy transfer with vertical nucleic acids (GETvNA), a method to investigate DNA–protein interactions that exploits the vertical orientation adopted by double-stranded DNA on graphene. This approach enables the dynamic study of DNA conformational changes via energy transfer from a probe dye to graphene, achieving spatial resolution down to the Ångström scale at subsecond temporal resolution. We measured DNA bending induced by adenine tracts, bulges, abasic sites and the binding of endonuclease IV. In addition, we observed the translocation of the O6-alkylguanine DNA alkyltransferase on DNA, reaching single base-pair resolution and detecting preferential binding to adenine tracts. This method promises widespread use for dynamical studies of nucleic acids and nucleic acid–protein interactions with resolution so far reserved for traditional structural biology techniques.
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U2 - 10.1038/s41592-024-02498-x
DO - 10.1038/s41592-024-02498-x
M3 - Article
C2 - 39516563
AN - SCOPUS:85208789416
SN - 1548-7091
VL - 22
SP - 135
EP - 144
JO - Nature Methods
JF - Nature Methods
IS - 1
M1 - eaan1133
ER -