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Detection of conformational and net charge differences in DNA-protein complexes by quantitative electrophoresis on polyacrylamitie-agarose copolymer gels
Journal article   Peer reviewed

Detection of conformational and net charge differences in DNA-protein complexes by quantitative electrophoresis on polyacrylamitie-agarose copolymer gels

L. Orbán, A. Chrambach, C. Zwieb and S.L. Adhya
Electrophoresis, Vol.12(6), pp.391-396
1991
DOI: https://doi.org/10.1002/elps.1150120602
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Abstract

The Galactosidase repressor (GalR) of Escherichia coli modulates the expression of the gal operon by binding to two DNA operators, OE and O1. The OE and O1 elements are 16 by pallindromic DNA sequences, differing in four of the base pairs (Fig. 1). OE and O1 DNA fragments, both free and complexed with repressor, were analyzed by “quantitative gel electrophoresis”. By the criteria of that method, applied to the linear Ferguson plots of both DNA fragments and the linear ranges of those of the DNA-GalR complexes, it was shown that the apparent size of DNA increases upon repressor binding. Moreover, this size increase is greater for the complex with the O1 operator than for the complex with the OE operator in the case that GalR is located in the center of a 155 bp DNA fragment. This is not the case when GalR is located in a peripheral position. By contrast with their size differences, the centrally located GalR-O1 and GalR-OE complexes appear to possess indistinguishable net surface charge densities as judged from the intercepts with the mobility axis. The larger size of the complex with centrally located O1 fragment, as compared with that bearing the OE fragment, is interpreted as being due to bending of the DNA-protein complex, since an authentically bent fragment of a plasmid with bent upstream activator sequence also exhibits a larger slope of the Ferguson plot, and thus the larger size, than predicted on the basis of its DNA chain length (bp). Thus, the apparently larger size of the GalR-O1 complex at the center of DNA, compared to that of the GalR-OE complex, supports the previous conclusion that the Gal repressor induces a larger degree of bending in O1 DNA than in OE DNA. DNA fragments bearing OE and O1 when complexed with the Gal repressor show convex Ferguson plots at polyacrylamide concentrations below that of gelation and in the presence of 0.5 % agarose, while the plots of the corresponding free 155 bp DNA fragments are linear in that range. The curvature presumably reflects the size increase concomitant with complex formation, since DNA larger than 155 bp also exhibits that curvature on polyacrylamide stabilized by nonrestrictive agarose gels.

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Collaboration types
International collaboration
Citation topics
1 Clinical & Life Sciences
1.42 Bacteriology
1.42.131 Bacterial Gene Regulation
Web Of Science research areas
Biochemical Research Methods
Chemistry, Analytical
ESI research areas
Chemistry
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