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Automated flow injection gradient technique for binding studies of micromolecules to proteins using potentiometric sensors: Application to bovine serum albumin with anilinonaphthalenesulfonate probe and drugs

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dc.contributor.author Georgiou, ME en
dc.contributor.author Georgiou, CA en
dc.contributor.author Koupparis, MA en
dc.date.accessioned 2014-06-06T06:44:01Z
dc.date.available 2014-06-06T06:44:01Z
dc.date.issued 1999 en
dc.identifier.issn 00032700 en
dc.identifier.uri http://dx.doi.org/10.1021/ac981019b en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/1622
dc.subject.other 8 anilino 1 naphthalenesulfonic acid en
dc.subject.other bovine serum albumin en
dc.subject.other article en
dc.subject.other automation en
dc.subject.other competitive inhibition en
dc.subject.other complex formation en
dc.subject.other flow injection analysis en
dc.subject.other fluorometry en
dc.subject.other potentiometry en
dc.subject.other protein analysis en
dc.subject.other protein binding en
dc.subject.other spectrophotometry en
dc.subject.other technique en
dc.subject.other Anilino Naphthalenesulfonates en
dc.subject.other Autoanalysis en
dc.subject.other Biosensing Techniques en
dc.subject.other Calibration en
dc.subject.other Flow Injection Analysis en
dc.subject.other Fluorescent Dyes en
dc.subject.other Indicators and Reagents en
dc.subject.other Pharmaceutical Preparations en
dc.subject.other Potentiometry en
dc.subject.other Proteins en
dc.subject.other Serum Albumin, Bovine en
dc.title Automated flow injection gradient technique for binding studies of micromolecules to proteins using potentiometric sensors: Application to bovine serum albumin with anilinonaphthalenesulfonate probe and drugs en
heal.type journalArticle en
heal.identifier.primary 10.1021/ac981019b en
heal.publicationDate 1999 en
heal.abstract An automated flow injection (FI) gradient technique is described for the binding study of the potentiometric probe 1-anilino-8-naphthalenesulfonate (ANS) to bovine serum albumin (BSA). Using a single-channel FI system with a mixing chamber and a flow ANS electrode, the binding parameters (binding constant and number of binding sites) were calculated using the Scatchard model. The concentration gradient was calibrated by injecting ANS in the stream, and the binding experiment was performed by injecting ANS-BSA solution in the carrier solution of equal albumin concentration. The equations describing the concentration gradient and the corresponding electrode potential curve are presented. A systematic study of the factors affecting the complexation equilibrium and the electrode response was performed. For the ANS binding to BSA, two binding classes were determined with binding constants of (2.1 ± 0.3) x 105 and (3.3 ± 0.8) x 103 M-1 and 3.8 ± 0.6 and 10 ± 2 binding sites per class, respectively, at 27 ± 1 °C, in 0.10 M phosphate pH 7.4. Competitive binding experiments of sulfamethoxazole, salicylate, azapropazone, ketoprofen and tolmetin to albumin were also performed by monitoring ANS binding inhibition (decrease of apparent binding constant). This technique takes advantage of FI gradients and direct potentiometry and utilizes the total information contained in FI peaks, providing fast and accurate binding information in a wide range of concentration ratios. en
heal.journalName Analytical Chemistry en
dc.identifier.issue 13 en
dc.identifier.volume 71 en
dc.identifier.doi 10.1021/ac981019b en
dc.identifier.spage 2541 en
dc.identifier.epage 2550 en


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