Van Dyke, Michael W. and Dervan, Peter B. (1983) Methidiumpropyl-EDTA•Fe(II) and DNase I footprinting report different small molecule binding site sizes on DNA. Nucleic Acids Research, 11 (16). pp. 5555-5567. ISSN 0305-1048. PMCID PMC326297. http://resolver.caltech.edu/CaltechAUTHORS:VANnar83
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DNase I and MPE.Fe (II) footprinting both employ partial cleavage of ligand-protected DNA restriction fragments and Maxam-Gilbert sequencing gel methods of analysis. One method utilizes the enzyme, DNase I, as the DNA cleaving agent while the other employs the synthetic molecule, methidium-propyl-EDTA (MPE). For actinomycin D, chromomycin A3 and distamycin A, DNase I footprinting reports larger binding site sizes than MPE.Fe (II). DNase I footprinting appears more sensitive for weakly bound sites. MPE.Fe (II) footprinting appears more accurate in determining the actual size and location of the binding sites for small molecules on DNA, especially in cases where several small molecules are closely spaced on the DNA. MPE.Fe (II) and DNase I report the same sequence and binding site size for lac repressor protein on operator DNA.
|Additional Information:||© 1983 IRL Press Limited, Oxford, England. Received 4 April 1983; Revised 5 July 1983; Accepted 21 July 1983. We are grateful to the National Institutes of Health for grant support (GM-27681) and a National Research Service Award (GM-07616) to MWV. Division of Chemistry and Chemical Engineering, Contribution Number 6797, California Institute of Technology, Pasadena, CA, 91125, USA|
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|PubMed Central ID:||PMC326297|
|Official Citation:||Michael W.Van Dyke and Peter B. Dervan Methidiumpropyl-EDTA-Fe(II) and DNase I footprinting report different small molecule binding site sizes on DNA Nucl. Acids Res. (1983) 11 (16): 5555-5567 doi:10.1093/nar/11.16.5555|
|Usage Policy:||No commercial reproduction, distribution, display or performance rights in this work are provided.|
|Deposited By:||Tony Diaz|
|Deposited On:||07 Aug 2006|
|Last Modified:||09 May 2016 18:15|
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