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1.
Angew Chem Int Ed Engl ; 62(39): e202307538, 2023 09 25.
Artigo em Inglês | MEDLINE | ID: mdl-37581373

RESUMO

Super-resolution techniques like single-molecule localisation microscopy (SMLM) and stimulated emission depletion (STED) microscopy have been extended by the use of non-covalent, weak affinity-based transient labelling systems. DNA-based hybrid systems are a prominent example among these transient labelling systems, offering excellent opportunities for multi-target fluorescence imaging. However, these techniques suffer from higher background relative to covalently bound fluorophores, originating from unbound fluorophore-labelled single-stranded oligonucleotides. Here, we introduce short-distance self-quenching in fluorophore dimers as an efficient mechanism to reduce background fluorescence signal, while at the same time increasing the photon budget in the bound state by almost 2-fold. We characterise the optical and thermodynamic properties of fluorophore-dimer single-stranded DNA, and show super-resolution imaging applications with STED and SMLM with increased spatial resolution and reduced background.


Assuntos
DNA , Imagem Individual de Molécula , Microscopia de Fluorescência/métodos , Imagem Individual de Molécula/métodos , Oligonucleotídeos
2.
J Phys Chem B ; 128(28): 6751-6759, 2024 Jul 18.
Artigo em Inglês | MEDLINE | ID: mdl-38955346

RESUMO

Protein labeling through transient and repetitive hybridization of short, fluorophore-labeled DNA oligonucleotides has become widely applied in various optical super-resolution microscopy methods. The main advantages are multitarget imaging and molecular quantification. A challenge is the high background signal originating from the presence of unbound fluorophore-DNA labels in solution. Here, we report the self-quenching of fluorophore dimers conjugated to DNA oligonucleotides as a general concept to reduce the fluorescence background. Upon hybridization, the fluorescence signals of both fluorophores are restored. We expand the toolbox of fluorophores suitable for self-quenching and report their spectra and hybridization equilibria. We apply self-quenched fluorophore-DNA labels to stimulated emission depletion microscopy and single-molecule localization microscopy and report improved imaging performances.


Assuntos
DNA , Corantes Fluorescentes , Microscopia de Fluorescência , Corantes Fluorescentes/química , DNA/química , Hibridização de Ácido Nucleico , Oligonucleotídeos/química
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