Determination of receptor protein binding site specificity and relative binding strength using a time-resolved competition assay
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25084055
DOI
10.1016/j.vascn.2014.07.006
PII: S1056-8719(14)00239-1
Knihovny.cz E-zdroje
- Klíčová slova
- Binding assay, Cetuximab, Competition assay, Competitor, EGF receptor, Methods, Panitumumab, TGF-α, Tracer,
- MeSH
- časové faktory MeSH
- cetuximab MeSH
- epidermální růstový faktor chemie metabolismus MeSH
- erbB receptory antagonisté a inhibitory chemie metabolismus MeSH
- humanizované monoklonální protilátky chemie farmakologie MeSH
- kompetitivní vazba účinky léků MeSH
- lidé MeSH
- ligandy MeSH
- monoklonální protilátky chemie farmakologie MeSH
- nádorové buňky kultivované MeSH
- panitumumab MeSH
- substrátová specifita MeSH
- transformující růstový faktor alfa chemie metabolismus MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- vztahy mezi strukturou a aktivitou MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cetuximab MeSH
- epidermální růstový faktor MeSH
- erbB receptory MeSH
- humanizované monoklonální protilátky MeSH
- ligandy MeSH
- monoklonální protilátky MeSH
- panitumumab MeSH
- transformující růstový faktor alfa MeSH
INTRODUCTION: Competitive binding assays can be used to decipher not only the binding kinetics of studied ligands but also the binding site preference. Such assays are an essential step in the characterization of radioligands. However, the currently used competition assays require high concentrations of usually expensive ligands and still provide only binding site preference. By employing the time-resolved competition assay presented in this paper, binding characteristics including binding site preference can be obtained using less ligand. METHODS: To demonstrate the appropriateness of the time-resolved competition assay, we developed an assay in which the ligand binding was interrupted with a competitor. Experiments were performed on human carcinoma cell lines expressing epidermal growth factor receptor (EGFR). The targeting of the receptor was performed with radio-iodinated epidermal growth factor (EGF). The employed competitors involved either natural ligand transforming growth factor alpha (TGF-α) or anti-EGFR antibodies cetuximab and panitumumab targeting the same EGFR domain. RESULTS: Radio-iodinated EGF bound to EGFR was displaced with either low concentrations of cetuximab or high concentrations of panitumumab. In the case of TGF-α, we observed no competitive displacement of bound EGF at either high or low concentrations. When comparing the time-resolved competition assay with a manual competition assay, the resulting data of measured inhibition constants were in agreement. DISCUSSION: The results summarised in this study confirm the appropriateness of the time-resolved competition assay for assessing ligand binding properties. The assay has the potential to complement or replace conventional competition assays for determining binding site preference in the future.
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