Ligand-binding assays with OBPs and CSPs

被引:20
|
作者
D'Onofrio, Chiara [1 ]
Zaremska, Valeriia [1 ]
Zhu, Jiao [1 ,2 ]
Knoll, Wolfgang [1 ,3 ]
Pelosi, Paolo [1 ]
机构
[1] AIT Austrian Inst Technol GmbH, Biosensor Technol, Tulln, Austria
[2] Johannes Gutenberg Univ Mainz, Inst Mol Physiol, Fac Biol, Mainz, Germany
[3] CEST Competence Ctr Electrochem Surface Technol, Tulln, Austria
关键词
NUCLEIC-ACID INTERACTIONS; REVERSE CHEMICAL ECOLOGY; PHEROMONE-BINDING; MICROSCALE THERMOPHORESIS; OLFACTORY RECEPTOR; ODORANT RECEPTORS; DEPENDENT BINDING; OPIATE RECEPTORS; PROTEIN; IDENTIFICATION;
D O I
10.1016/bs.mie.2020.05.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Assessing the ligand-binding properties of OBPs and CSPs is essential for understanding their physiological function. It also provides basic information when these proteins are used as biosensing elements for instrumental measurement of odors. Although different approaches have been applied in the past to evaluate the affinity of receptors and soluble binding proteins to their ligands, using a fluorescent reporter represents the method of choice for OBPs and CSPs. It offers the advantages of working at the equilibrium, being simple, fast and inexpensive, without requiring the use of radioactive tracers. However, as an indirect method, the fluorescence competitive binding approach presents drawbacks and sometimes requires an elaborate analysis to explain unexpected results. Here, after a brief survey of the different approaches to evaluate affinity constants, we focus on the fluorescence binding assay as applied to OBPs and CSPs, discussing situations that may require closer inspection of the results.
引用
收藏
页码:229 / 258
页数:30
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