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Covalent binding represents a logical approach for modifying the surface properties of a biomaterial, allowing the bulk composition to remain unchanged, whilst surface functionality is engineered to afford a more desirable characteristic.
We describe a rapid, systematic and general approach for modifying a surface in such a way that an enzyme can both bind tightly to the surface and maintain or even enhance its activity.
Herein, we report a novel and powerful approach for modifying neuron-surface interfaces using mussel-inspired polymer ('polydopamine film polyDA)') for generating effective chemical platforms on both electrode and insulator surfaces simultaneously.
This novel strategy could be a potential valuable therapeutic approach for modifying NK cells.
This approach for modifying the Ni-MoS2 interface opens a promising new path for reducing the impact of contacts on MoS2 FET performance.
Directed evolutionary strategy36,37,38,39 was adopted as the engineering approach for modifying the substrate-binding sites of KGSADH.
Potentially, our approach for modifying LFP cathode materials could also be applied in modifying other cathodes for commercial LIBs.
An efficient remeshing approach for modified solid models using existing prior existing meshes is proposed in this paper to resolve this issue.
We recently reported an approach for incorporating dialkylglycerol modified oligonucleotides (DAG) into cell membranes.
Here, we describe production of transmitochondrial mice harboring foreign mitochondrial genomes and related targeting approaches for modifying mitochondrial gene function.
We describe approaches for modifying the thermodynamics and kinetics of hydrogen sorption reactions in light-metal hydrides.
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CEO of Professional Science Editing for Scientists @ prosciediting.com