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Fluorescence Correlation Spectroscopy (FCS) is the simplest of such technique and is commonly used to observe binding interactions or the diffusion of fluorescent particles in vitro or in vivo [ 3– 5].
On the other hand, 'shape shifter' allosteric inhibitors that exploit active site flexibility to perturb subsite binding interactions or the catalytic centre are promising avenues for new MMPI development.
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We note that the scaffold can contribute to bioactivity directly, via shape or binding interactions, or indirectly, via functionalization potential.
These results suggest that, although Ras Cys has no role in either the wt Ras GDP binding interaction or in the O2–- and Cdc25-mediated wt Ras GDP dissociation, the Ras residue Cys is involved in the O2 -mediated inhibitiO2 -mediatedtalytinhibitionof Cdc25 on Ras.
In this sense, the binding of low-affinity nickel to the surface of NikR could help tune the affinity of NikR for the nik operon in response to the nickel concentration in the cell, either by facilitating the NikR−DNA binding interaction or by stabilizing the bound NikR−DNA complex.
Current methods, including isocratic elution, equilibrium filtration, and in-line probing, typically rely on intrinsic fluorescence properties of the target or labeling that risks altering the binding interaction or limits method scalability and are often restricted to specific reaction conditions or exhibit limited sensitivity.
We do this in a way that is similar to HSQC chemical-shift mapping [ 23], which is performed when binding interactions occur in the fast or slow exchange regimes on the chemical-shift time scale.
Lastly, a crystal structure of idelalisib bound to the p110δ subunit of PI3Kδ furthers our understanding of the binding interactions that confer the potency and selectivity of idelalisib.
Renda, M. et al. Critical DNA binding interactions of the insulator protein CTCF: a small number of zinc fingers mediate strong binding, and a single finger-DNA interaction controls binding at imprinted loci.
Importantly, the presentation of thus immobilized glycosides makes them available to specific lectin-glycan binding interactions at the polymer-solution interface while, in the absence of specific binding interactions, leads to a reduction in albumin adsorption.
Moesin could be involved in the dynamic restructuring of such microdomains by regulating binding interactions between the plasma membrane and the actin cytoskeleton.
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