Sentence examples for bonding affinity of the from inspiring English sources

The grafted zwitterionic polymer brushes not only effectively templated the surface mineralization, increasing the surface mineral coverage by >100% from those achieved with unmodified Ti6Al4V substrate, but also significantly improved the bonding affinity of the surface apatite minerals to the metallic substrate.

The resultant cobalt ion concentrations were lower than expected before the synthesis, which was most likely related to differences in the constant bonding and chemical affinity of the ions of cobalt (II) and calcium (II).

Furthermore, the cysteine at VL85 of ds-FV57 was mutated to serine to construct ds-FV57VL85Ser in order to avoid potential mis-formed disulfide bonds which would alter the affinity of the scFv.

Finally, we do not exclude that the affinity of the chemical bond between the palmitic acid moiety and the peptide backbone might be slightly different during the synthesis of the linear HER-GLP-1 versus the branched HER-GLP-2.

To the extent that axial water "competes" for heme ligation with these drugs, the energy of the water-iron bond contributes to the apparent binding affinity of the drug.

The small peak right at threshold (0 eV) is most likely an artefact and reminiscent to the peculiarities of DEA.[ 1] The reaction enthalpy (Δ H°) for the DEA reactions (3a) and (3b) is given by the D(C=NO2) bond dissociation energy minus the electron affinity of the fragment on which the excess electron finally becomes localized.

The cause of this bias is most likely a lack of probe saturation in low DNA quantity samples and inflated intensities due to a higher binding affinity of the triple hydrogen bonding of guanine to cytosine.

Directionality in these redox reactions is determined by thermodynamic favorability through electron affinity of the potential disulfide bonds.

However, hydrogen bonding to TM5 may still enhance the binding affinity of the agonists.

Molecular surface analysis with the MOLCAD program reveals that electrostatic interactions (including hydrogen bonds) and Van der Waals forces contribute to the affinity of the hexapeptide for α-amylase.

Early work characterizing the binding properties of the α7-nAChR showed that modification of receptor thiol groups and cleavage of disulfide bonds, important in the manifestation of affinity state changes, decreases the binding affinity of the receptor for agonists by 10-fold, shifting the dose-response curve to the right [77].