A critical view on the analysis of fluorescence quenching data for determining ligand-protein binding affinity
被引:54
|
作者:
Bakar, Khairul Azreena
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机构:
Univ Kebangsaan Malaysia, Fac Sci & Technol, Ctr Biotechnol & Funct Foods, Bangi 43600, Selangor, MalaysiaUniv Kebangsaan Malaysia, Fac Sci & Technol, Ctr Biotechnol & Funct Foods, Bangi 43600, Selangor, Malaysia
Bakar, Khairul Azreena
[1
]
Feroz, Shevin Rizal
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机构:
Univ Kebangsaan Malaysia, Fac Sci & Technol, Ctr Biotechnol & Funct Foods, Bangi 43600, Selangor, MalaysiaUniv Kebangsaan Malaysia, Fac Sci & Technol, Ctr Biotechnol & Funct Foods, Bangi 43600, Selangor, Malaysia
Feroz, Shevin Rizal
[1
]
机构:
[1] Univ Kebangsaan Malaysia, Fac Sci & Technol, Ctr Biotechnol & Funct Foods, Bangi 43600, Selangor, Malaysia
Fluorescence data analysis;
Ligand-protein interaction;
Association constant;
Phenylbutazone;
Human serum albumin;
HUMAN-SERUM-ALBUMIN;
DRUG;
PHENYLBUTAZONE;
SITE;
AGENT;
HSA;
D O I:
10.1016/j.saa.2019.117337
中图分类号:
O433 [光谱学];
学科分类号:
0703 ;
070302 ;
摘要:
The past decade has seen an increase in the number of research papers on ligand binding to proteins based on fluorescence spectroscopy. In most cases, determination of the binding affinity is made by analyzing the quenching of protein fluorescence induced by the ligand. However, many such articles, even those published in reputed journals, suffer from several mistakes with regard to analysis of fluorescence quenching data. Using the binding of phenylbutazone to human serum albumin as a model, we consider some of these mistakes and show how they affect the values of the association constant. In particular, the failure to correct for the inner filter effect and the use of unsuitable equations are discussed. Ligand binding data presented in these articles should be treated with caution, especially in the absence of data from complementary techniques. (C) 2019 Elsevier B.V. All rights reserved.