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Biology subjects

Gregory, R. C.

Publications and source records attributed to Gregory, R. C..

2 recordsLinked to original sources

Spatially patterned, spectral single-molecule microscopy

Multicolour and spectrally resolved single-molecule microscopy can reveal molecular interactions, nanoscale environments and dynamics, but usually depends on experimentally complex detection architectures based on beam splitting, spectral dispersion or engineered point spread functions. Here we show that spatially patterned detectors offer a conceptually simpler route to spectral single-molecule imaging. By replacing a conventional monochrome camera with a commercially available colour CMOS detector and fitting the raw detector response directly, we recover both molecular position and spectral fingerprint from a single image without optical splitting, channel registration or demosaicing. We term this approach spatial spectral single-molecule microscopy, or S3M. We show that S3M retains single-molecule sensitivity across the visible spectrum, enables robust spectral multiplexing, and supports applications spanning multicolour single-molecule tracking, single-molecule F&oumlrster resonance energy transfer, multicolour localisation microscopy and spectral PAINT. Although spatial patterning necessarily trades photon efficiency for spectral information, current low noise detectors already provide sufficient performance for a broad range of experiments. Spatially patterned detection therefore establishes a widely accessible strategy for simplified spectral microscopy and single-molecule spectroscopy, and points towards a new class of detector informed photonic measurement schemes for nanoscale imaging.

biophysics↗

Multiplexed Digital Characterisation of Misfolded Protein Oligomers via Solid-State Nanopores

Misfolded protein oligomers are of central importance in both the detection and treatment of Alzheimers and Parkinsons diseases. However, accurate high-throughput methods to identify and quantify oligomer populations are currently lacking. We present here a single-molecule approach for the detection of oligomeric species. The approach is based on the use of solid state nanopores and multiplexed DNA barcoding to identify and characterise oligomers from multiple samples. We study -synuclein oligomers in the presence of several small molecule inhibitors of -synuclein aggregation, as an illustration of the applicability of this method to assist the development of diagnostic and therapeutic methods for Parkinsons disease.

biophysics↗