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The model of the molecular recognition interface was constructed and analyzed.
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Here, we also discuss molecular recognition at the interface of self-assembled monolayers and liquids.
Molecular recognition in the interface assembling P5 RNA and ΔP5 RNA is strong and specific, and the catalytic ability of the two-piece ribozyme is comparable to that of the parent unimolecular ribozyme.
Given the ever-increasing number of crystal structures in the public domain, we believe that the application of similar analyses of crystal-packing interactions has the potential to provide further valuable insights into molecular recognition at protein protein interfaces.
However, molecular recognition based on chemical interfaces relying on weak interactions is not specific enough to produce unique response pattern even in an array format.
Moreover, the variation in the molecular recognition properties of the interfaces may also provide a qualitative explanation to the observed variety of oligomerization mechanisms and oligomeric structures [14].
The PCDS does not use any chemical receptors or interfaces for molecular recognition.
In particular the analysis of the new turn classification could be of interest, since β-turns are known to play a central role as molecular recognition elements in protein-protein interfaces and binding of peptide hormones to their receptors [4] and could be essential for the optimal sidechain conformation within ligand binding.
Inspired by nature's elegant hierarchical organization, we mimic the molecular-scale interactions that are built upon molecular recognition and self-assembly at surfaces and interfaces.
Thus, lipid membrane doped with Pt nanoparticles is a novel electrode system at nanoscale that can penetrate through the insulating membrane to probe molecular recognition and catalytic events at the lipid membrane solution interface.
Binding to the biomaterial interface is achieved using a molecular recognition domain specific for the titanium/titanium alloy implant surface and a biochemical signal guiding stem cells to differentiate by activating the Wnt signaling pathway for bone formation.
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