Sentence examples for binding affinity of both from inspiring English sources

We investigated the possibility of separated coating formation of Al as Al2O3 and F as LiF from AlF3 using density functional theory calculation, which suggests a favorable binding affinity of both Al2O3 and LiF phases to the OLO surface to support the preferable formation of coating layer of Al2O3 and LiF.

The present study aimed at the establishment of two novel experimental approaches for the assessment of binding affinity of both, radiolabelled and non-labelled compounds targeting the A3R, based on high-resolution real-time data acquisition of radioligand-receptor binding kinetics.

In the present study, we successfully designed and established two experimental approaches for the reliable in vitro assessment of binding affinity of both, radiolabelled and non-labelled compounds, based on high-resolution real-time data acquisition of radioligand-receptor binding kinetics.

Twelve classical phenotypes with high content validity map to the Comt locus (p<0.02, Table S2), including binding affinity of both dopamine receptors (DRD1 and DRD2) in caudate, nucleus accumbens, ventral tegmental area, and prefrontal cortex [19].

On the other hand the human receptor binding affinity of both CkPA04-TLS (Kd' ∼3 pM) and CkPA04-RTLS (Kd' ∼8 pM) were several fold higher than that of CkPA04-LS and in the same range as that of Alb58 HA.

It might be speculated that altered fibrin in hyperglycemia leads to lower binding affinity of both tissue plasminogen activator and plasminogen toward fibrin (11) and, as a consequence, impaired clot lysis in our assay.

Finally, peroxisome proliferator activated receptor gamma (PPARγ) binding activity was measured to check the binding affinities of both TGZ and TSN.

We find that the binding affinities of both RecBC and RecBCD for a DNA end are unaffected upon substituting PEG for the ssDNA between the sixth and the final two nucleotides of the 3′- dT n tail.

It comes as a surprise that the mutation of Glu119 that can form strong H-bonds with the inhibitors in the wild-type protein does not have direct impact on the binding affinities of both OTV and PRV due to the regulation of the strong unfavorable polar desolvation energies.

To further determine the specific binding affinities of both native CN and VCN to purified (αvβ3 and αvβ5) or recombinant (α5β1) functional integrins, we measured these interactions in solution by fluorescence polarization.

Since eIF3f serves as a connecting platform between mTOR-raptor and S6K1 in muscle cells (Figure 2) and mutation of the C-terminal lysines in eIF3f increases phosphorylation of S6K1, we assessed the binding affinities of both eIF3f wt and mutant eIF3f K5–10R proteins with S6K1 and mTOR-raptor.