Characterization of Intracellular Crowding Environments with Topology-Based DNA Quadruplex Sensors

• Published in: Analytical chemistry (Washington) 2019-02, Vol.91 (4), p.2586-2590
• Main Authors: Takahashi, Shuntaro, Yamamoto, Johtaro, Kitamura, Akira, Kinjo, Masataka, Sugimoto, Naoki
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Biomolecules; Chemistry; Cytosol; Deoxyribonucleic acid; Dependence; Dielectric constant; DNA; Energy transfer; Fluorescence resonance energy transfer; Guanine; Nuclei (cytology); Nucleoli; Polyethylene glycol; Sensors; Structure-function relationships; Topology; Water activity
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.8b04177

Molecular crowding creates a unique environment in cells and imposes physical constraints such as the excluded volume effect, water activity, and dielectric constant that can affect the structure and function of biomolecules. It is therefore important to develop a method for quantifying the effects of molecular crowding in cells. In this study, we developed a Förster resonance energy transfer (FRET) probe based on a guanine-quadruplex (G4) DNA motif that shows distinct FRET signals in response to crowding conditions in the presence of salt and poly­(ethylene glycol). FRET efficiencies varied in different solutions, reflecting the dependence of G4 stability and topology on salt concentration and water activity. In living cells, FRET signals in the nucleus were higher than those in the cytosol; the signals in membraneless nuclear compartments (i.e., nucleolus) were especially high, suggesting that a decrease in water activity is important for the crowding effect in the nucleus. Thus, the use of DNA sensors with variable structures can elucidate the local effects of molecular crowding in cells.