The COVID-19 pandemic has highlighted the urgent need for sensitive, affordable, and widely accessible testing at the point of care. Here we demonstrate a new, universal LFA platform technology using...

The structure and dynamics of polyelectrolytes differ from those of neutral polymers. How these differences affect the transport of anisotropic particles remains incompletely understood. Here, we investigate the transport of semiflexible M13 bacteriophage (phage) in aqueous semidilute solutions of sodium polystyrenesulfonate (PSS) with various ionic strengths using fluorescence microscopy. We tune the characteristic length scales of the PSS using two molecular weights of 68 and 2200 kDa and by varying the ionic strength of the solutions from 10 −6 to 10 −1 M. Phage exhibit diffusive dynamics across all polymer concentrations. For 2200 kDa PSS solutions, the phage dynamics monotonically deviate from the bulk prediction as polymer concentration increases and exhibit non-Gaussian distributions of displacements. Existing scaling theories can approximately collapse dynamics as a function of phage hydrodynamic radius to polymer size ratio R h /ξ onto a master curve across polymer concentrations and ionic strengths. This partial collapse, however, does not follow the prediction for diffusion of isotropic particles in flexible Gaussian chains, suggesting the presence of multiple diffusive modes due to the anisotropic structure of the phage and the confining length scales set by the structure and dynamics of charged polymers.

The COVID-19 pandemic has highlighted the urgent need for sensitive, affordable, and widely-accessible testing at the point-of-care. Here we report the development of a sensitive chemiluminescence-based smartphone-readable lateral flow assay for the detection of SARS-CoV-2 nucleoprotein using M13 phage conjugated with antibodies and HRP enzymes as LFA reporter particles. We screened 84 anti-nucleoprotein monoclonal antibody pairs in phage LFA and identified an antibody pair that gave an LoD of 25 pg/mL nucleoprotein in nasal swab extract using a FluorChem gel documentation system and 100 pg/mL when the test was imaged and analyzed by an in-house-developed smartphone reader. The smartphone-read LFA signals for positive clinical samples tested (N = 15, with known Ct) were statistically different (p < 0.001) from negative clinical samples tested (N = 11). The translation-ready phage LFA technology combined with smartphone chemiluminescence imaging can enable the timely development of ultrasensitive, affordable point-of-care testing platforms for SARS-CoV-2 and beyond.