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The system is composed of four modules: initialization, hand gesture recognition, interaction control and system settings.
After a few minutes, DA molecules were absorbed on the surface of MNPs through molecular recognition interaction between DA and β-CD.
This study confirmed the highly specific molecular recognition interaction between the streptavidin on the surface and the biotin-conjugated BSA [79].
The phosphorylated serine 58 and serine 62 on TAZ create an N-terminal phosphodegron for β-TrCP recognition, interaction and further polyubiquitylation and degradation of TAZ (Huang et al., 2012).
This can be designed by various approaches, e.g.: (i) using a natural ligand-protein complex as a template; (ii) applying the principle of complementarity to exposed residues of the protein structure; and (iii) mimicking directly a natural biological recognition interaction.
In this manuscript we propose a simple and efficient strategy to improve the sensitivity of localized surface plasmon resonance (LSPR) shift-based biosensors using biotin-streptavidin recognition interaction as a proof-of-concept.
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Upon start codon recognition, interactions involving eIF5, and ultimately 3c0:eIF1 association, facilitate eIF1 release.
Molecular docking studies were performed to understand the molecular recognition interactions and this knowledge was used to identify the potent inhibitors using virtual screening.
A peptidomimetic derived from these Nbs can be considered to be a small peptide mimicking some of the molecular recognition interactions of a natural peptide or protein in a three-dimensional (3D) space, with a receptor that has improved properties.
The extracellular domains of these receptor proteins are involved in ligand-binding specificity as well as pathogen recognition interactions.
Indeed, in the absence of detailed knowledge of ligand receptor recognition interactions for AT2R, identification of AT2R-selective ligands came after long and delicate synthetic efforts.
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