A Versatile Virus-Mimetic Engineering Approach for Concurrent Protein Nanocage Surface-Functionalization and Cargo Encapsulation.

Naturally occurring protein nanocages like ferritin are self-assembled from multiple subunits. Because of their unique cage-like structure and biocompatibility, there is a growing interest in their biomedical use. A multipurpose and straightforward engineering approach does not exist for using nanocages to make drug-delivery systems by encapsulating hydrophilic or hydrophobic drugs and developing vaccines by surface functionalization with a protein like an antigen. Here, a versatile engineering approach is described by mimicking the HIV-1 Gap polyprotein precursor. Various PREcursors of nanoCages (PREC) are designed and created by linking two ferritin subunits via a flexible linker peptide containing a protease cleavage site. These precursors can have additional proteins at their N-terminus, and their protease cleavage generates ferritin-like nanocages named protease-induced nanocages (PINCs). It is demonstrated that PINC formation allows concurrent surface decoration with a protein and hydrophilic or hydrophobic drug encapsulation up to fourfold more than the amount achieved using other methods. The PINCs/Drug complex is stable and efficiently kills cancer cells. This work provides insight into the precursors' design rules and the mechanism of PINCs formation. The engineering approach and mechanistic insight described here will facilitate nanocages' applications in drug delivery or as a platform for making multifunctional therapeutics like mosaic vaccines.

The modeling and analysis of the COVID-19 pandemic with vaccination and isolation: a case study of Italy.

The global spread of COVID-19 has not been effectively controlled. It poses a significant threat to public health and global economic development. This paper uses a mathematical model with vaccination and isolation treatment to study the transmission dynamics of COVID-19. In this paper, some basic properties of the model are analyzed. The control reproduction number of the model is calculated and the stability of the disease-free and endemic equilibria is analyzed. The parameters of the model are obtained by fitting the number of cases that were detected as positive for the virus, dead, and recovered between January 20 and June 20, 2021, in Italy. We found that vaccination better controlled the number of symptomatic infections. A sensitivity analysis of the control reproduction number has been performed. Numerical simulations demonstrate that reducing the contact rate of the population and increasing the isolation rate of the population are effective non-pharmaceutical control measures. We found that if the isolation rate of the population is reduced, a short-term decrease in the number of isolated individuals can lead to the disease not being controlled at a later stage. The analysis and simulations in this paper may provide some helpful suggestions for preventing and controlling COVID-19.

Fibers with Hyper-Crosslinked Functional Porous Frameworks.

The incorporation of robust porous frameworks into polymer fibers with handleable morphologies and flexible chemical compositions exhibits significant advantages for device fabrication in a wide range of applications. However, the soft linear polymeric chains of the fibers make the generation of nanopores extremely challenging. Herein, a facile synthetic strategy based on a combination of functional monomer grafting and hyper-crosslinking technology is developed for the porous engineering of polymeric fibers. In this methodology, the nanoporous framework originating from the hyper-crosslinking of aromatic monomers is covalently grafted onto fibers, which is beneficial to retaining their unique fiber morphology and to preserving their excellent mechanical properties. Moreover, this promising protocol can be further extended to the porous functionalization of polymeric matrices with diverse morphologies for target-specific applications.

Electrostatic-Assisted Liquefaction of Porous Carbons.

Porous liquids are a newly developed porous material that combine unique fluidity with permanent porosity, which exhibit promising functionalities for a variety of applications. However, the apparent incompatibility between fluidity and permanent porosity makes the stabilization of porous nanoparticle with still empty pores in the dense liquid phase a significant challenging. Herein, by exploiting the electrostatic interaction between carbon networks and polymerized ionic liquids, we demonstrate that carbon-based porous nanoarchitectures can be well stabilized in liquids to afford permanent porosity, and thus opens up a new approach to prepare porous carbon liquids. Furthermore, we hope this facile synthesis strategy can be widely applicated to fabricate other types of porous liquids, such as those (e.g., carbon nitride, boron nitride, metal-organic frameworks, covalent organic frameworks etc.) also having the electrostatic interaction with polymerized ionic liquids, evidently advancing the development and understanding of porous liquids.

Surfactant-Assisted Stabilization of Au Colloids on Solids for Heterogeneous Catalysis.

The stabilization of surfactant-assisted synthesized colloidal noble metal nanoparticles (NPs, such as Au NPs) on solids is a promising strategy for preparing supported nanocatalysts for heterogeneous catalysis because of their uniform particle sizes, controllable shapes, and tunable compositions. However, surfactant removal to obtain clean surfaces for catalysis through traditional approaches (such as solvent extraction and thermal decomposition) can easily induce the sintering of NPs, greatly hampering their use in synthesis of novel catalysts. Such unwanted surfactants have now been utilized to stabilize NPs on solids by a simple yet efficient thermal annealing strategy. After being annealed in N2 flow, the surface-bound surfactants are carbonized in situ as sacrificial architectures that form a conformal coating on NPs and assist in creating an enhanced metal-support interaction between NPs and substrate, thus slowing down the Ostwald ripening process during post-oxidative calcination to remove surface covers.

Guest-Induced Breathing Effect in a Flexible Molecular Crystal.

By introducing a flexible component into a molecular building block, we present an unprecedented alkyl-decorated flexible crystalline material with a breathing behavior. Its selective adsorption is derived from the breathing effect induced by a guest triggered alkyl transformation. This feature allows the crystal to take up 2.5 mmol g(-1) of chloroform with high adsorption selectivity (CHCl3 /EA >2000 for example), implying a potential application in sorption separation and chemical sensors.

Hierarchical assembly of a dual-responsive macroscopic insulated molecular wire bundle in a gradient system.

Here, we report the hierarchical self-assembly of a cationic gemini amphiphile, Azo 1, in a composition gradient solution generated using solvent evaporation. As the gradient solution is formed, Azo 1 forms nanorods in the lower region of the solution. Depending on solvent composition, these nanorods can further develop into nanofibres, which can then intertwine to form double helices and other types of nanohelices in the upper region of the solution. Finally, a macroscopic wire bundle is formed via the fusion of nanohelices; this ribbon-like bundle exhibits elasticity and linear ohmic resistance properties. More intriguingly, this bundle exhibits photoresponsive properties that affect its deformation and conductivity, as well as a rapid electroresponse that affects its conductivity, indicating that it is feasible to control the charge pathway.

Synthesis and optoelectrochemical properties of ZnS:Mn nanocrystals.

Mn2+ ions doped ZnS semiconductor nanocrystals (ZnS:Mn NCs) were synthesized using colloidal chemical method at 70 degrees C without any capping agents. The as-prepared undoped ZnS and ZnS:Mn NCs were characterized by UV-Vis absorption spectra, fluorescent emission spectra, X-ray powder diffraction (XRD), inductively coupled plasma analysis (ICP), X-ray photoelectron spectroscopy (XPS), Dynamic light scattering (DLS), cyclic voltammogram and electronic transmission microscopy (TEM). The dependence of photoluminescence of ZnS:Mn NCs on dopant concentration was studied. The results show that Mn2+ ions mainly stay at ZnS nanocystal surface, and Mn2+-surface defect state complex was formed, as a result of which, surface defect emission of ZnS nanocrystals was substituted with Mn2+-related PL emission. The strongest fluorescent emission intensity was obtain at 1.85 at% Mn2+ doped ZnS:Mn NCs. The Mn2+ doped ZnS:Mn NCs are of 5 nm in diameter. The emission peak at 575 nm is attributed to d-d (4T1 --> 6A1) transition of Mn2+ ions. The existence of Mn2+-related photoluminescence could be well correlated with cyclic voltammogram of Mn2+-doped NCs, where pair of oxidation and reduction peaks were clearly observed due to the doped Mn2+ ions. The adsorbed Mn2+ ions on ZnS NCs produced neither Mn2+ emission nor redox peaks. For heavily doped ZnS:Mn NCs (4.87 at%), redox peaks gap in cyclic voltammogram became larger and new oxidation peak appeared. Correspondingly, when the Mn2+ doping concentration reached 4.87 at%, the Mn2+-related emission totally disappears due to the Mn-Mn interactions. This work implys that electrochemical technique is possibly an useful tool to probe the local structure of doped Mn2+ ions.