Abstract
In single molecule fluorescence studies, background emission from labeled substrates often restricts their concentrations to non-physiological nanomolar values. One approach to address this challenge is the use of zero-mode waveguides (ZMWs), nanoscale holes in a thin metal film that physically and optically confine the observation volume allowing much higher concentrations of fluorescent substrates. Standard fabrication of ZMWs utilizes slow and costly E-beam nano-lithography. Herein, ZMWs are made using a self-assembled mask of polystyrene microspheres, enabling fabrication of thousands of ZMWs in parallel without sophisticated equipment. Polystyrene 1 μm dia. microbeads self-assemble on a glass slide into a hexagonal array, forming a mask for the deposition of metallic posts in the inter-bead interstices. The width of those interstices (and subsequent posts) is adjusted within 100–300 nm by partially fusing the beads at the polystyrene glass transition temperature. The beads are dissolved in toluene, aluminum or gold cladding is deposited around the posts, and those are dissolved, leaving behind an array ZMWs. Parameter optimization and the performance of the ZMWs are presented. By using colloidal self-assembly, typical laboratories can make use of sub-wavelength ZMW technology avoiding the availability and expense of sophisticated clean-room environments and equipment.
Highlights
Single molecule fluorescence techniques are valuable tools in biophysical research
In single molecule fluorescence studies, such as smFRET, background fluorescence from labeled substrates often requires their use at concentrations several orders of magnitude less than present in vivo
That shortcoming can be addressed through the use of zero-mode waveguides that attenuate background fluorescence by restricting the observation volume
Summary
Single molecule fluorescence techniques are valuable tools in biophysical research. By avoiding the averaging inherent in bulk measurements, they can distinguish subpopulations of molecules, directly observe the trajectory and timing of enzymatic reaction steps without needing to synchronize a population, and can enable study of rare events and conformational fluctuations [1]. All single-molecule fluorescence techniques require careful optimization of signal-to-noise ratio due to their inherently limited signal.
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