Single-molecule detection schemes offer powerful means to overcome static and dynamic heterogeneity inherent to complex samples. However, probing biomolecular interactions and reactions with high throughput and time resolution remains challenging, often requiring surface-immobilized entities. Here, we introduce glass-made nanofluidic devices for the high-throughput detection of freely-diffusing single biomolecules by camera-based fluorescence microscopy. Nanochannels of 200 nm height and a width of several micrometers confine the movement of biomolecules. Using pressure-driven flow through an array of parallel nanochannels and by tracking the movement of fluorescently labelled DNA oligonucleotides, we observe conformational changes with high throughput. In a device geometry featuring a T-shaped junction of nanochannels, we drive steady-state non-equilibrium conditions by continuously mixing reactants and triggering chemical reactions. We use the device to probe the conformational equilibrium of a DNA hairpin as well as to continuously observe DNA synthesis in real time. Our platform offers a straightforward and robust method for studying reaction kinetics at the single-molecule level.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c8lc01175cDOI Listing

Publication Analysis

Top Keywords

single biomolecules
8
glass-made nanofluidic
8
nanofluidic devices
8
high throughput
8
high-throughput non-equilibrium
4
non-equilibrium studies
4
studies single
4
biomolecules glass-made
4
devices single-molecule
4
single-molecule detection
4

Similar Publications

The crowded bacterial cytoplasm is composed of biomolecules that span several orders of magnitude in size and electrical charge. This complexity has been proposed as the source of the rich spatial organization and apparent anomalous diffusion of intracellular components, although this has not been tested directly. Here, we use biplane microscopy to track the 3D motion of self-assembled bacterial genetically encoded multimeric nanoparticles (bGEMs) with tunable size (20 to 50 nm) and charge (-3,240 to +2,700 e) in live cells.

View Article and Find Full Text PDF

Analysis of Drug Molecules in Living Cells.

Crit Rev Anal Chem

January 2025

Department of Bioengineering, Faculty of Engineering, The University of Edinburgh, Edinburgh, UK.

Cells are the fundamental units of life, comprising a highly concentrated and complex assembly of biomolecules that interact dynamic ally across spatial and temporal scales. Living cells are constantly undergoing dynamic processes, therefore, to understand the interactions between drug molecules and living cells is of paramount importance in the biomedical sciences and pharmaceutical development. Compared with traditional end-point assays and fixed cell analysis, analysis of drug molecules in living cells can provide more insight into the effects of drugs on cells in real-time and allowing for a better understanding of drug mechanisms and effects, which will contribute to the development of drug developing and testing and personalize medicine.

View Article and Find Full Text PDF

Conventional methods for extracting rare earth metals (REMs) from mined mineral ores are inefficient, expensive, and environmentally damaging. Recent discovery of lanmodulin (LanM), a protein that coordinates REMs with high-affinity and selectivity over competing ions, provides inspiration for new REM refinement methods. Here, we used quantum mechanical (QM) methods to investigate trivalent lanthanide cation (Ln) interactions with coordination systems representing bulk solvent water and protein binding sites.

View Article and Find Full Text PDF

Critical review of the criterion of polysaccharide purity.

Carbohydr Polym

March 2025

School of Chinese Medicine, Hong Kong Baptist University, 999077, Hong Kong. Electronic address:

Natural polysaccharides attract scientists and industries' interest with diverse applications in biomaterials, immune regulation, gut microbiota regulation, food additives, and more. Nevertheless, the absence of standardized purity criteria created significant challenges in characterizing polysaccharides, leading to varied and complicated structures, and impeding progress in research and development. Consequently, it is essential to obtain samples that adhere to high-level and unified purity standards for effective polysaccharide research.

View Article and Find Full Text PDF

An erbium-doped fiber ring laser based on a single-mode fiber-no-core fiber-single-mode fiber (SMF-NCF-SMF) structure was constructed and experimentally demonstrated for label-free DNA hybridization measurement. The SMF-NCF-SMF structure acts as a sensing element and a filter to select the laser wavelength. The proposed fiber ring laser sensor exhibits a high optical signal-to-noise ratio (SNR, >50 dB) and narrow full width at half maximum (FWHM, <0.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!