The phrase "a suitable receptor" is correct and usable in written English.
It can be used in contexts related to biology, chemistry, or pharmacology when discussing a receptor that is appropriate for a specific ligand or signal.
Example: "In drug development, identifying a suitable receptor is crucial for ensuring the efficacy of the treatment."
Alternatives: "an appropriate receptor" or "a fitting receptor".
This link provides an NH group that can form a hydrogen bond to a suitable acceptor atom and an oxygen atom, which can act as a suitable receptor.
As expected, the analysis of the results confirmed that true binders were ranked at the first positions, when a suitable receptor conformation was used.
A particularly simple arrangement that is compatible with our data is the coupling of one end of a magnetosome chain to mechanically-activated ion channels in a suitable receptor cell [12], [41].
Due to the restricted expression of αvβ3 in tumours, αvβ3 is considered a suitable receptor for tumour targeting.
The restricted expression of integrin αv β3 in tumors makes it a suitable receptor for tumor targeting.
As the residues in the binding domain have no significant variation, the crystallography structure of TRAF6 protein is a suitable receptor for docking simulation.
It presents the many merits and feasibilities of drug localization and target identification through the use of a suitable technique: receptor microautoradiography. Studies of drug targets and target bioavailability require methods with high resolution and sensitivity to gain information for understanding mechanisms of action, sound modeling, prediction of effects, and toxicity.
Hence, ER retention of PrP∗ in Tmp21 knockdown cells could be due simply to the lack of a suitable export receptor.
Presently this is difficult because there is not a suitable MT1 receptor antibody and because of low levels of MT1 mRNA [ 42].
Because availability of suitable receptor can determine efficiency of infection, altered levels of cell surface sialic acid may affect the susceptibility to influenza viruses, especially for α2,3-linked sialic acid, which is scarce in upper airway and if upregulated may enhance susceptibility to H5N1 AIV.
When molecular dynamics simulations of insufficient length are used to identify cryptic sites, allosteric sites, or pharmacologically relevant binding-pocket conformations for virtual-screening projects, the risk is that some suitable receptor conformations will be missed.
