## Abstract Comparative studies on the interaction of 8โanilinoโ1โnaphthalenesulfonate (ANS) with polylysine and polyarginine have been made by equilibrium dialysis and fluorescence or circular dichroism measurements, to investigate the structural characteristics of the polypeptides. The results ar
Interaction of 8-anilino-1-naphthalenesulfonate with 2,6-di-O-methylcyclomaltoheptaose
โ Scribed by Juziro Nishijo; Mayumi Nagai; Masako Yasuda
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 830 KB
- Volume
- 245
- Category
- Article
- ISSN
- 0008-6215
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โฆ Synopsis
The interaction of 8-anilino-1-naphthalenesulfonate CANS) with 2,6-di-O-methyl-cyclomaltoheptaose (2,6-DM$CD) was investigated in a 0.1 M phosphate buffer at pH 7.4 by fluorescence spectrophotometry. Utilizing the fact that the fluorescence intensity of ANS increases in the presence of 2,6-DM-PCD, the thermodynamic parameters for inclusion complex formation were determined as follows: AGo= -10.3 kJ.mol-' at 25ยฐC AH"= -13.4 kJ.mol-', As"= -10.9 J.degg'.mol-'.
The main driving force for the inclusion complex formation was considered to be the Van der Waals-London dispersion forces, while the contribution of the hydrophobic interaction was small. Also, from the measurements of proton nuclear magnetic resonance spectra and studies with Corey-Pauling-Koltun models, the probable structure was determined.
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The proton magnetic resonance (PMR) and phosphorus magnetic resonance (PhMR) spectra of egg phosphatidylcholine in the presence of l-anilino-8-naphthalenesulfonate (ANS) have been studied. At low ratios of ANS to phospholipid, the spectra indicate that ANS molecules are in the lipid interface region
## Abstract 8โAnilinoโ1โnaphthalenesulfonic acid (ANS) is a popular fluorescence probe, broadly used for the analysis of proteins, but the nature of its interaction with proteins and the high increase in the fluorescence intensity that takes place upon such process are still unclear. In the last fe
## Abstract The addition of the fluorescent dye, ANS, to intact ascites tumor cells results in an enhancement of fluorescence intensity. The increase in fluorescence intensity as a function of time is biphasic which suggests that at least two processes occur. The first associated with the rapid ini