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John H. Connor

Publications and source records attributed to John H. Connor.

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Single virus fingerprinting by widefield interferometric defocus-enhanced mid-infrared photothermal microscopy

Clinical identification and fundamental study of viruses rely on the detection of viral proteins or viral nucleic acids. Yet, amplification-based and antigen-based methods are not able to provide precise compositional information of individual virions due to small particle size and low-abundance chemical contents (e.g., ~ 5000 proteins in a vesicular stomatitis virus). Here, we report a widefield interferometric defocus-enhanced mid-infrared photothermal (WIDE-MIP) microscope for high-throughput fingerprinting of single viruses. With the identification of feature absorption peaks, WIDE-MIP reveals the contents of viral proteins and nucleic acids in single DNA vaccinia viruses and RNA vesicular stomatitis viruses. Different nucleic acids signatures of thymine and uracil residue vibrations are obtained to differentiate DNA and RNA viruses. WIDE-MIP imaging further reveals an enriched \b{eta} sheet components in DNA varicella-zoster virus proteins. Together, these advances open a new avenue for compositional analysis of viral vectors and elucidating protein function in an assembled virion.

physics.optics

Vibrational Spectroscopic Detection of Single Virus by a Confocal Interferometric Mid-Infrared Photothermal Microscope

We report a confocal interferometric mid-infrared photothermal (MIP) microscope and its application to label-free detection of biological nanoparticles down to single virus level. We apply the interferometric scattering principle to detect the weak photothermal effect induced by infrared absorption in a viral particle. We validated this method with two kinds of viruses, namely the vesicular stomatitis virus (VSV) and poxvirus. The single virus spectra generated by MIP microscopy show high consistency in the same group, with dominant peaks contributed by the amide I and amide II vibrations. The ratio of these two peaks are significantly different between VSV and poxvirus, highlighting the potential of using MIP microscopy for label-free differentiation of viral particles. This all-optical chemical imaging method opens a new way for spectroscopic detection of biological nanoparticles in a label-free manner and may facilitate in predicting and controlling outbreaks of emerging virus strains.

physics.app-ph