Concentration-Related Response Potentiometric Titrations To Study the Interaction of Small Molecules with Large Biomolecules

被引:11
|
作者
Hamidi-Asl, Ezat [1 ]
Daems, Devin [2 ,3 ]
De Wael, Karolien [1 ]
Van Camp, Guy [3 ]
Nagels, Luc J. [2 ]
机构
[1] Univ Antwerp, AXES Res Grp, B-2020 Antwerp, Belgium
[2] Univ Antwerp, Dept Chem, B-2020 Antwerp, Belgium
[3] Univ Antwerp, Dept Biomed Sci, Ctr Med Genet, B-2610 Antwerp, Belgium
关键词
ION-SELECTIVE ELECTRODES; BINDING; PROTEIN; SENSOR; CHROMATOGRAPHY; RECOGNITION; STABILITY; DRUGS; DNA;
D O I
10.1021/ac503385x
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present paper, the utility of a special potentiometric titration approach for recognition and calculation of biomolecule/small-molecule interactions is reported. This approach is fast, sensitive, reproducible, and inexpensive in comparison to the other methods for the determination of the association constant values (K-a) and the interaction energies (Delta G). The potentiometric titration measurement is based on the use of a classical polymeric membrane indicator electrode in a solution of the small-molecule ligand. The biomolecule is used as a titrant. The potential is measured versus a reference electrode and transformed into a concentration-related signal over the entire concentration interval, also at low concentrations, where the millivolt (y-axis) versus log c(analyte) (x-axis) potentiometric calibration curve is not linear. In the procedure, K-a is calculated for the interaction of cocaine with a cocaine binding aptamer and with an anticocaine antibody. To study the selectivity and cross-reactivity, other oligonucleotides and aptamers are tested, as well as other small ligand molecules such as tetrakis(4-chlorophenyl)borate, metergoline, lidocaine, and bromhexine. The calculated K-a compared favorably to the value reported in the literature using surface plasmon resonance. The potentiometric titration approach called concentration-related response potentiometry is used to study molecular interaction for seven macromolecular target molecules and four small-molecule ligands.
引用
收藏
页码:12243 / 12249
页数:7
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