Fluorescence quenching to study protein-ligand binding: common errors
- PMID: 19997966
- DOI: 10.1007/s10895-009-0572-x
Fluorescence quenching to study protein-ligand binding: common errors
Erratum in
- J Fluoresc. 2011 Nov;21(6):2245
Abstract
A number of recent articles, amongst others several published in the Journal of Fluorescence, use inappropriate fluorescence methodology to determine ligand binding characteristics to (mostly) proteins. In this Letter, several common pitfalls are discussed in relation to two recent publications in the Journal of Fluorescence (Wang et al. (2009) 19:801-808; Ding et al. (2009) 19:783-791). The Author hopes that this contribution helps to prevent a further spread of the incorrect methodology, and results in a reappraisal of those articles already published using similar methodology.
Comment on
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A study of the interaction between malachite green and lysozyme by steady-state fluorescence.J Fluoresc. 2009 Sep;19(5):783-91. doi: 10.1007/s10895-009-0475-x. Epub 2009 Mar 31. J Fluoresc. 2009. PMID: 19333739
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Study on the binding behavior of lysozyme with cephalosporin analogues by fluorescence spectroscopy.J Fluoresc. 2009 Sep;19(5):801-8. doi: 10.1007/s10895-009-0477-8. Epub 2009 Apr 3. J Fluoresc. 2009. PMID: 19343485
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