ABSTRACT
The chemistry of aptamers is largely limited to natural nucleotides, and although modifications of nucleic acids can enhance target aptamer affinity, there has not yet been a technology for selecting the right modifications in the right locations out of the vast number of possibilities, because enzymatic amplification does not transmit sequence-specific modification information. Here we show the first method for the selection of specific nucleoside modifications that increase aptamer binding efficacy, using the oncoprotein EGFR as a model target. Using fluorescence-activated bead sorting (FABS), we have successfully selected optimized aptamers from a library of >65 000 variations. Hits were identified by tandem mass spectrometry and validated by using an EGFR binding assay and computational docking studies. Our results provide proof of concept for this novel strategy for the selection of chemically optimised aptamers and offer a new method for rapidly synthesising and screening large aptamer libraries to accelerate diagnostic and drug discovery.
ABSTRACT
Caloric materials have attracted significant interest as replacements for conventional refrigeration, which is becoming increasingly important in our daily lives, yet poses issues for sustainability due to both energy consumption and loss of refrigerants into the atmosphere. Among caloric materials, which are key to solid state cooling technologies, those exhibiting the magnetocaloric effect (MCE), an entropy-driven phenomenon under cycled applied magnetic fields, are promising candidates for cryogenic cooling. These have potential to replace conventional cryogenics, particularly liquid He - an increasingly scarce and expensive resource. Amongst magnetocalorics, coordination polymers containing polyatomic ligands have been shown to be very promising materials due to their large entropy changes at low temperatures. One of the contributing factors to this peformance is their unique structural flexibility, as they can adopt a wide range of structures usually not accessible for conventional materials, such as close-packed metal oxides. The most researched materials for magnetocaloric applications are those containing Gd as their magnetic centre, as the combination of structure and the weakly interacting 4f orbitals of Gd3+ in these materials enables the fabrication of promising magnetocalorics that contain a high density of cations and thus exhibit a high entropy change as a function of their weight and volume at ultra-low cryogenic temperatures. Alongside this, there is a growing interest in magnetocaloric coordination polymers with their magnetocaloric effect optimised for lower applied fields that can be generated using permanent magnets through incorporating other magnetic cations, including lanthanides with greater magnetic anisotropy. When combined with tailored magnetic interactions this leads to promising entropy changes above 4 K, a typical base temperature for many cryogenic applications. This review discusses the most promising magnetocalorics among coordination polymers and MOFs, highlighting their structural characteristics, and concluding with a brief perspective on the future of this field.
ABSTRACT
We present a study on the nuclear and magnetic structures of two iron-based garnets with magnetic cations isolated on tetrahedral sites. Ca2YZr2Fe3O12 and Ca2LaZr2Fe3O12 offer an interesting comparison for examining the effect of increasing cation size within the diamagnetic backbone of the garnet crystal structure, and how such changes affect the magnetic order. Despite both systems exhibiting well-pronounced magnetic transitions at low temperatures, we also find evidence for diffuse magnetic scattering due to a competition between the nearest-neighbor, next nearest-neighbor, and so on, within the tetrahedral sites. This competition results in a complex noncollinear magnetic structure on the tetrahedral sublattice creating a mixture of ferro- and antiferromagnetic interactions above the long-range ordering temperature near 20 K and suggests that the cubic site of the garnet plays a significant role in mediating the superexchange interactions between tetrahedral cations.
