Smooth deuterated cellulose films for the visualisation of adsorbed bio-macromolecules.

Novel thin and smooth deuterated cellulose films were synthesised to visualize adsorbed bio-macromolecules using contrast variation neutron reflectivity (NR) measurements. Incorporation of varying degrees of deuteration into cellulose was achieved by growing Gluconacetobacter xylinus in deuterated glycerol as carbon source dissolved in growth media containing D2O. The derivative of deuterated cellulose was prepared by trimethylsilylation(TMS) in ionic liquid(1-butyl-3-methylimidazolium chloride). The TMS derivative was dissolved in toluene for thin film preparation by spin-coating. The resulting film was regenerated into deuterated cellulose by exposure to acidic vapour. A common enzyme, horseradish peroxidase (HRP), was adsorbed from solution onto the deuterated cellulose films and visualized by NR. The scattering length density contrast of the deuterated cellulose enabled accurate visualization and quantification of the adsorbed HRP, which would have been impossible to achieve with non-deuterated cellulose. The procedure described enables preparing deuterated cellulose films that allows differentiation of cellulose and non-deuterated bio-macromolecules using NR

ECoR: Energy-Aware Collaborative Routing for Task Offload in Sustainable UAV Swarms

In this work, we propose an Energy-aware Collaborative Routing (ECoR) scheme for optimally handling task offloading between source and destination UAVs in a grid-locked UAV swarm. We divide the proposed scheme into two parts -- routing path discovery and routing path selection. The scheme selects the most optimal path between a source and destination from a massive set of all possible paths, based on the maximization of residual energy of UAVs along a selected path. This routing path selection ensures balanced energy utilization between members of the UAV swarm and enhances the overall path lifetime without incurring additional delays in doing so. Actual readings from our small-scale UAV swarm testbed are utilized to emulate a large-scale scenario and analyze the behavior of our proposed scheme. Upon comparison of the ECoR scheme with broadcast-based routing and the shortest path based routing, we observe better sustainability regarding the longevity of the UAV lifetimes in the swarm, optimized individual UAV, as well as reduced collective path-based energy consumption, all the while having comparable transmission delays to the shortest path based scheme

Visualization and Quantification of IgG Antibody Adsorbed at the Cellulose-Liquid Interface.

Quantification of adsorbed biomolecules (enzymes, proteins) at the cellulose interface is a major challenge in developing eco-friendly biodiagnostics. Here, a novel methodology is developed to visualize and quantify the adsorption of antibody from solution to the cellulose-liquid interface. The concept is to deuterate cellulose by replacing all nonexchangeable hydrogens from the glucose rings with deuterium in order to enhance the scattering contrast between the cellulose film surface and adsorbed antibody molecules. Deuterated cellulose (DC) was obtained from bacterial (Gluconacetobacter xylinus strain) cellulose, which was grown in heavy water (D2O) media with a deuterated glycerol as a carbon source. For comparison, hydrogenated cellulose (HC) was obtained from cellulose acetate. Both HC and DC thin films were prepared on silicon substrate by spin coating. X-ray reflectivity (XR) shows the formation of homogeneous and smooth film. Neutron reflectivity (NR) at the liquid/film interface reveals swelling of the cellulose film by a factor of 2-3× its initial thickness. An Immunoglobulin G (IgG), used as a model antibody, was adsorbed at the liquid-solid interface of cellulose (HC) and deuterated cellulose (DC) films under equilibrium and surface saturation conditions. NR measurements of the IgG antibody layer adsorbed onto the DC film can clearly be visualized, in sharp contrast in comparison to the HC film. The average thickness of the IgG adsorbed layer onto cellulose films is 127 ± 5 Å and a partial monolayer is formed. Visualization and quantification of adsorbed IgG is shown by large difference in scattering length density (SLD) between DC (7.1 × 10-6 Å-2) and IgG (4.1 × 10-6 Å-2) in D2O, which enhanced the scattering contrast in NR. Quartz crystal measurements (QCM-D) were used as a complementary method to NR to quantify the adsorbed IgG over the cellulose interface

Bio-deuterated cellulose thin films for enhanced contrast in neutron reflectometry

Novel molecularly smooth, flat and thin films of regenerated bio-deuterated cellulose were produced for enhanced contrast with adsorbed molecules in neutron reflectivity (NR) and for cellulose structure studies. The cellulose films were produced to study both the solid/air interface and the solid/liquid interface. Cellulose films with a wide range of scattering contrast were achieved by combining exchange of 1H for deuterium on hydroxyl groups via water in the liquid phase and via biosynthesis of deuterated bacterial cellulose by Gluconacetobacter xylinus which can deuterate the hydrogens bonded to carbon atoms in cellulose. The deuterated cellulose combined with NR will help to provide new information on the interaction of various (bio)-macromolecules and cellulose. This includes quantifying and visualizing the density profile of polymers and biomolecules adsorbed onto cellulose surface. The potential of this material for IR studies of materials adsorbed to cellulose films is briefly discussed

Rapid Gel Card Agglutination Assays for Serological Analysis Following SARS-CoV-2 Infection in Humans

High-throughput and rapid serology assays to detect the antibody response specific to severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) in human blood samples are urgently required to improve our understanding of the effects of COVID-19 across the world. Short-term applications include rapid case identification and contact tracing to limit viral spread, while population screening to determine the extent of viral infection across communities is a longer-term need. Assays developed to address these needs should match the ASSURED criteria. We have identified agglutination tests based on the commonly employed blood typing methods as a viable option. These blood typing tests are employed in hospitals worldwide, are high-throughput, fast (10-30 min), and automated in most cases. Herein, we describe the application of agglutination assays to SARS-CoV-2 serology testing by combining column agglutination testing with peptide-antibody bioconjugates, which facilitate red cell cross-linking only in the presence of plasma containing antibodies against SARS-CoV-2. This simple, rapid, and easily scalable approach has immediate application in SARS-CoV-2 serological testing and is a useful platform for assay development beyond the COVID-19 pandemic