1991
DOI: 10.1021/ja00018a019
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Long-range fluorescence quenching of ethidium ion by cationic porphyrins in the presence of DNA

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Cited by 215 publications
(120 citation statements)
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“…(3) originated from the sphere of action quenching mechanism, which involves defining a critical distance within which the excited energy of the fluorophore is totally deactivated by the quencher. 24 Calculated σ values with respect to Ca 2+ concentration are shown in Figure 2(b). In the absence of Ca 2+ , the critical distance was 9.5 base-pairs or 32.3 Å, slightly larger than the 25-30 Å reported by Pasternak et al 24 The difference may have been due to the differences in the experimental conditions, such as the nature and concentration of the buffer.…”
Section: Resultsmentioning
confidence: 99%
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“…(3) originated from the sphere of action quenching mechanism, which involves defining a critical distance within which the excited energy of the fluorophore is totally deactivated by the quencher. 24 Calculated σ values with respect to Ca 2+ concentration are shown in Figure 2(b). In the absence of Ca 2+ , the critical distance was 9.5 base-pairs or 32.3 Å, slightly larger than the 25-30 Å reported by Pasternak et al 24 The difference may have been due to the differences in the experimental conditions, such as the nature and concentration of the buffer.…”
Section: Resultsmentioning
confidence: 99%
“…24 Calculated σ values with respect to Ca 2+ concentration are shown in Figure 2(b). In the absence of Ca 2+ , the critical distance was 9.5 base-pairs or 32.3 Å, slightly larger than the 25-30 Å reported by Pasternak et al 24 The difference may have been due to the differences in the experimental conditions, such as the nature and concentration of the buffer. The distance increased almost linearly with increasing Ca 2+ concentration up to 40 mM, above which the slope flattened.…”
Section: Resultsmentioning
confidence: 99%
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“…However, EB, which is one of the most sensitive fluorescence probes, emits intense fluorescence in the presence of DNA due to its strong intercalation between the adjacent DNA base pairs [43] and this enhanced fluorescence could be quenched by the addition of another molecule [44] owing to the decreasing binding sites of DNA available for EB. [44,45] Thus, EB can be used to probe the interaction of complexes with DNA. If the complex can intercalate into DNA, it will lead to a decrease in the binding sites of DNA available for EB, and hence to a quenching of fluorescence intensity of the EB-DNA system.…”
Section: Eb Fluorescence Displacement Assaymentioning
confidence: 99%
“…Fluorescence spectroscopy was also applied to study the interactions of these porphyrin dimers with DNA [26]. The fluorescence emission spectra of 4a -4c (l em,max ¼ 659, 656, and 655 nm, resp.)…”
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confidence: 99%