Sentence examples for examine the binding of from inspiring English sources
We chose to examine the binding of the [Lys]-fullerene to Kv1.3, giving us the opportunity to directly compare our results with the binding of polypeptide toxins [37, 38].
Furthermore, FST315 and FST288 have been shown to bind to other TGF-beta superfamily member proteins, such as BMP-6 and MBP-7 (Sidis et al. 2006), and current study did not examine the binding of FST-type proteins to other TGB-beta superfamily member proteins.
To examine the binding of YY1 to the PSMD8 promoter in vivo, we employed chromatin immunoprecipitation assays using antibodies against YY1 and non-relevant antibodies as a control.
Using specific antibodies, we were able to examine the binding of Sp1 and Sp3 proteins, which are highly conserved and ubiquitously expressed in murine and human cell lines [71], to these sites.
All members of the DNA-PK complex except for Ku70 were identified as binding partners of dysbindin-1, which led us to examine the binding of Ku70/80 to dysbindin-1.
To determine whether DRIL1 sumoylation modulates this interaction, we performed an electromobility shift assay (EMSA) to examine the binding of wild-type and non-sumoylable DRIL1 to two oligonucleotides representing prototypic DRIL1 binding sites (bf150 and TX125, respectively [6]).
The model system was further validated by examining the binding of one of the Opa proteins found in Neisseria and known to bind to human CEACAM1.
Employing a solid phase microplate-binding assay, we examined the binding of each viral ligand to wild type gC1qR and 11 gC1qR deletion mutants.
In the current studies we examined the binding of endogenous ligands, artificial ligands, and potent endocrine-disrupting chemicals to wild-type and Asp351 mutants of the human estrogen receptor-α ligand-binding domain.
With this goal in mind, we examined the binding of kanamycin A and four derivatives (the products of enzymic turnovers of kanamycin A by aminoglycoside-modifying enzymes) to a 27 nucleotide RNA representing the bacterial ribosomal A site.
We recently developed non-secosteroidal VDR ligands based on a carbon-containing boron cluster, 1,12-dicarba-closo-dodecaborane (p-carborane), and examined the binding of one of them to VDR by means of crystallographic analysis.
