Isoperimetric inequalities for an electrostatic problem

We study the problem of the (p-)capacity cp of a multiconnected configuration Ω = (G E) (∪ Hi) when ∂G and ∂E have given potentials. Here Ω represents a nonhomogeneous medium and the Hi, which separate the different connected components of Ω, represent perfect conductors. By comparison with a similar configuration with spherical symmetry, we give isoperimetric inequalities for cp and the unknown potentials on Hi

Generation of a neutralizing antibody against RD114-pseudotyped viral vectors

The feline endogenous RD114 glycoprotein has proved to be an attractive envelope to pseudotype both retroviral and lentiviral vectors. As a surface protein, its detection on packaging cells as well as viral particles would be useful in different fields of its use. To address this, we generated a monoclonal antibody against RD114 by immunization of rats, termed 22F10. Once seroconversion was confirmed, purified 22F10 was cloned into murine Fc and characterized with a binding affinity of 10nM. The antibody was used to detect RD114 and its variant envelopes on different stable viral packaging cell lines (FLYRD18 and WinPac-RD). 22F10 was also shown to prevent the infections of different strains of RD-pseudotyped vectors but not related envelope glycoproteins by blocking cell surface receptor binding. We are the first to report the neutralization of viral particles by a monoclonal αRD114 antibody

Anisotropic composite polymer for high magnetic force in microfluidic systems

International audienceAnisotropic carbonyl iron-PolyDiMethylSiloxane (PDMS) composites were developed and implemented in microfluidic devices to serve as magnetic flux concentrators. These original materials provide technological solutions for heterogeneous integration with PDMS. Besides microfabrication advantages, they offer interesting modular magnetic properties. Applying an external magnetic field during the PDMS reticulation leads to the formation of 1D-agglomerates of magnetic particles, organized in the non-magnetic polymer matrix. This induces an increase of susceptibility as compared to composites with randomly dispersed particles. In this report, we explored the gain in reachable magnetophoretic forces in operating microfluidic devices, from the study of magnetic micro-beads motion injected in the microchannel. We show that even at relatively large distances from the magnetically-functionalized channel wall, the anisotropic composite leads to a factor two increase in the magnetophoretic force. Finally, further investigations based on finite element description suggest that the measured benefit of anisotropic composite polymers does not only rely on the global susceptibility increase but also on the local magnetic field gradients originating from the microstructure

Quasilinear Dirichlet problem in a periodically perforated domain

Consider the following quasilinear Dirichlet problem (Pε) -Δp uε = fε in Ωε = Ω Tε uε = 0 on ∂ Ωε where 1 < p ≤ 2, (fε) a sequence of functions in Lp\u27(Ω) such that fε → f in Lp\u27(Ω) where p\u27 is the conjugate of p, Ω is a bounded domain in RN (N ≥ 2) and Tε the union of inclusions contained in Ω which are ε-periodically distributed. In this paper we give the limit problem and errors estimates for the problem (Pε)

Optimised Method for the Production and Titration of Lentiviral Vectors Pseudotyped with the SARS-CoV-2 Spike

The use of recombinant lentivirus pseudotyped with the coronavirus Spike protein of SARS-CoV-2 would circumvent the requirement of biosafety-level 3 (BSL-3) containment facilities for the handling of SARS-CoV-2 viruses. Herein, we describe a fast and reliable protocol for the transient production of lentiviruses pseudotyped with SARS-CoV-2 Spike (CoV-2 S) proteins and green fluorescent protein (GFP) reporters. The virus titer is determined by the GFP reporter (fluorescent) expression with a flow cytometer. High titers (>1.00 E+06 infectious units/ml) are produced using codon-optimized CoV-2 S, harbouring the prevalent D614G mutation and lacking its ER retention signal. Enhanced and consistent cell entry is achieved by using permissive HEK293T/17 cells that were genetically engineered to stably express the SARS-CoV-2 human receptor ACE2 along with the cell surface protease TMPRSS2 required for efficient fusion. For the widespread use of this protocol, its reagents have been made publicly available. Graphic abstract: Production and quantification of lentiviral vectors pseudotyped with the SARS-CoV-2 Spike glycoprotein