Title
Hydrophobic catalysis and a potential biological role of DNA unstacking induced by environment effects
Date Issued
27 August 2019
Access level
open access
Resource Type
journal article
Author(s)
Feng B.
Sosa R.P.
Mårtensson A.K.F.
Jiang K.
Tong A.
Dorfman K.D.
Takahashi M.
Lincoln P.
Westerlund F.
Nordén B.
University of California
Publisher(s)
National Academy of Sciences
Abstract
Hydrophobic base stacking is a major contributor to DNA double-helix stability. We report the discovery of specific unstacking effects in certain semihydrophobic environments. Water-miscible ethylene glycol ethers are found to modify structure, dynamics, and reactivity of DNA by mechanisms possibly related to a biologically relevant hydrophobic catalysis. Spectroscopic data and optical tweezers experiments show that base-stacking energies are reduced while base-pair hydrogen bonds are strengthened. We propose that a modulated chemical potential of water can promote “longitudinal breathing” and the formation of unstacked holes while base unpairing is suppressed. Flow linear dichroism in 20% diglyme indicates a 20 to 30% decrease in persistence length of DNA, supported by an increased flexibility in single-molecule nanochannel experiments in poly(ethylene glycol). A limited (3 to 6%) hyperchromicity but unaffected circular dichroism is consistent with transient unstacking events while maintaining an overall average B-DNA conformation. Further information about unstacking dynamics is obtained from the binding kinetics of large thread-intercalating ruthenium complexes, indicating that the hydrophobic effect provides a 10 to 100 times increased DNA unstacking frequency and an “open hole” population on the order of 10−2 compared to 10−4 in normal aqueous solution. Spontaneous DNA strand exchange catalyzed by poly(ethylene glycol) makes us propose that hydrophobic residues in the L2 loop of recombination enzymes RecA and Rad51 may assist gene recombination via modulation of water activity near the DNA helix by hydrophobic interactions, in the manner described here. We speculate that such hydrophobic interactions may have catalytic roles also in other biological contexts, such as in polymerases.
Start page
17169
End page
17174
Volume
116
Issue
35
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular Biología celular, Microbiología Ingeniería química
Scopus EID
2-s2.0-85071396992
PubMed ID
Source
Proceedings of the National Academy of Sciences of the United States of America
ISSN of the container
00278424
Sponsor(s)
ACKNOWLEDGMENTS. This work was supported by Swedish Research Council Grant 2015-04020 (to B.N.); Swedish Research Council Grant 2015–5062 and Olle Engqvist Foundation Grant 2016/84 (to F.W.); NIH Grant R01-HG006851 (to K.D.D.); and NIH Grant R01GM032543 and US Department of Energy Office of Basic Energy Sciences Nanomachine Program Contract DE-AC02-05CH11231 (to C.J.B.). We thank Irfan Shaukat for early work (2010).
Sources of information: Directorio de Producción Científica Scopus