Sentence examples for binding affinity conferred by from inspiring English sources

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Specifically, cardiac thin filament activation was enhanced through adenovirus-mediated over-expression of a cardiac troponin C (cTnC) variant designed to have increased Ca2 + binding affinity conferred by single amino acid substitution (L48Q).

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ADP and ATP, but not adenosine or nicotinamide mononucleotide [NMN+ (see Figure 1)], have been reported to inhibit the FeCN reaction, and ADP and ATP were reported to bind to the reduced flavin site and to stimulate the reduction of HAR, suggesting that the nucleotide binding affinities are conferred by specific parts of the nucleotide molecules.

This is consistent with competitive inhibition in which the inhibitor interferes with the catalytic properties of enzyme by affecting substrate binding affinity by conferring a Ki of 2.7 mM.

This research demonstrates that a single Nanobody target binding domain suffices and confers equal or higher affinity binding compared to published data of therapeutic monoclonal antibodies, where bivalent binding is conferred by four domains [ 24].

However, a significant drawback for the widespread application of ZFN technology is the limited binding selectivity conferred by the zinc-finger modules, as well as complex context-dependent interactions between adjacent zinc fingers that can alter binding affinity to the DNA (Cornu et al., 2008; Händel et al., 2009).

This spatial immobilization, coupled with the temporal differences in binding conferred by differential affinities, provides the first step towards the design of spatially and temporally controlled drug delivery from matrices.

DOI: http://dx.doi.org/10.7554/eLife.00691.010 To further analyze the apparent membrane affinity loss conferred by PTEN tail phosphorylation, we explored the binding interactions of semisynthetic PTENs with vesicles containing anionic phospholipids.

The competition experiment showed that the binding capability was conferred by the peptide sequence.

Thus, the binding affinity and selectivity conferred on the NetrinG NGL interaction by the specificity determinants we have identified provide the properties necessary to generate and maintain the reported compartmentalization of NGL1 and NGL2 to distinct dendritic subdomains, as proposed for a 'lock-in' type model (Nishimura-Akiyoshi et al, 2007).

We identify that the global stabilization of GALC conferred by azasugar derivatives, measured by fluorescence-based thermal shift assays, is directly related to their binding affinity, measured by enzyme inhibition.

The MBD is unusual among site-specific DNA binding proteins in that (i) specificity is not conferred by the enhanced affinity for the specific site but rather by suppression of its affinity for generic DNA, (ii) its specific binding to mCpG is highly electrostatic, and (iii) it takes up as well as displaces monovalent cations upon DNA binding.

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