2002
DOI: 10.1016/s0021-9673(02)01592-3
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Interaction between netropsin and double-stranded DNA in capillary zone electrophoresis and affinity capillary electrophoresis

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Cited by 20 publications
(21 citation statements)
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“…In sharp contrast, the intercalators showed preference for GC over AT sequences, in good agreement with the conclusions of previous reports [111,124]. Using CZE and ACE, the binding constant of a 14-mer dsDNA-netropsin interaction has been determined [21,116]. marker, and a negatively charged molecule, o-toluic acid (OTA), was chosen to indicate the change of EOF ( but not the EOF itself).…”
Section: Dna-small Molecule Interactionsupporting
confidence: 76%
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“…In sharp contrast, the intercalators showed preference for GC over AT sequences, in good agreement with the conclusions of previous reports [111,124]. Using CZE and ACE, the binding constant of a 14-mer dsDNA-netropsin interaction has been determined [21,116]. marker, and a negatively charged molecule, o-toluic acid (OTA), was chosen to indicate the change of EOF ( but not the EOF itself).…”
Section: Dna-small Molecule Interactionsupporting
confidence: 76%
“…The interaction between HSA and VO 21 or VO 3 2 was studied using CZE. VO 3 2 has only a weak binding affinity (6.0610 3 M 21 ) to HSA, but VO 21 (the reduced form of VO 3 2 ) binds to HSA with two strong affinities (K 1 = 1.2610 8 M 21 , K 2 = 8.5610 5 M 21 ) [93]. In ACE, the migration time of four compounds (warfarin, ibuprofen, surprofen, and flurbiprofen) was measured in the presence of normal or modified HSA (at tryptophan 214 or tyrosine 411).…”
Section: Protein-small Molecule Interactionmentioning
confidence: 99%
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“…Based on the CZE/FA method, the peak height changes of receptor (or ligand) resulting from interacting with ligand (or receptor) can be used to estimate the binding constant [40,41]. Previous reports have successfully estimated the binding constants of two fast binding kinetic systems, TrpRS-tRNA [39], DNA-netropsin [42]. From this study, we demonstrated that fast on-and-off kinetic interactions could also be studied by CZE, but not only by ACE.…”
Section: Discussionmentioning
confidence: 99%
“…CE has been used in a wide range of binding studies, employing chiral selectors to study the interaction of drug stereoisomers with other enantiomeric molecules [26], and investigating the interaction between biologically important molecules, such as lectin-carbohydrate [27], protein-ligand [28,29], drug-protein [30][31][32][33][34][35], DNA-ovalbumin [36], and DNA-drug [37]. Many recent reviews [38][39][40][41] report on the application of CE for binding studies, highlighting the advantages and some of the encountered limitations.…”
Section: Introductionmentioning
confidence: 99%