Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Jul 11:10:1589-95.
doi: 10.3762/bjoc.10.164. eCollection 2014.

Influence of perylenediimide-pyrene supramolecular interactions on the stability of DNA-based hybrids: Importance of electrostatic complementarity

Affiliations

Influence of perylenediimide-pyrene supramolecular interactions on the stability of DNA-based hybrids: Importance of electrostatic complementarity

Christian B Winiger et al. Beilstein J Org Chem. .

Abstract

Aromatic π-π stacking interactions are ubiquitous in nature, medicinal chemistry and materials sciences. They play a crucial role in the stacking of nucleobases, thus stabilising the DNA double helix. The following paper describes a series of chimeric DNA-polycyclic aromatic hydrocarbon (PAH) hybrids. The PAH building blocks are electron-rich pyrene and electron-poor perylenediimide (PDI), and were incorporated into complementary DNA strands. The hybrids contain different numbers of pyrene-PDI interactions that were found to directly influence duplex stability. As the pyrene-PDI ratio approaches 1:1, the stability of the duplexes increases with an average value of 7.5 °C per pyrene-PDI supramolecular interaction indicating the importance of electrostatic complementarity for aromatic π-π stacking interactions.

Keywords: DNA; hybridization; nucleic acids; perylenediimide; pyrene.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(A) Structures of 1,8-dialkynylpyrene (Y) and PDI (E); (B) illustration of the electrostatic potential surface of 1,8-diprop-1-ynylpyrene (left) and N,N’-dimethyl-PDI (right); (C) illustration of duplex formation with chimeric oligomers; (D) hybrids 1*2 to 1*6. The number of pyrene–PDI interactions increases from left to right.
Figure 2
Figure 2
A plot of melting temperature (Tm) versus the number of pyrene–PDI interactions for duplexes 1*2 to 1*6 (from left to right) presented in Table 1. The Tm was recorded at 260 nm; R2 = 0.987. The red triangle represents the Tm of the control hybrid 7*6.
Figure 3
Figure 3
UV–vis absorption spectra (scaled) of duplexes 1*2 (blue) and 1*6 (red) at 20 °C. Conditions: see Table 1.
Figure 4
Figure 4
UV–vis absorption spectra (scaled) of duplexes 1*2 to 1*6 at 20 °C. Conditions: see Table 1.
Figure 5
Figure 5
Temperature-dependent UV–vis absorption spectrum of 1*2. Conditions: see Table 1.
Figure 6
Figure 6
Fluorescence spectra of oligomer 1 (black), duplex 1*2 (blue) and duplex 1*6 (red) at 20 °C. Excitation: 370 nm. Conditions: see Table 1.
Figure 7
Figure 7
PAGE experiment. All oligomers were used in a total amount of 150 pmol in 10 mM sodium phosphate buffer, 100 mM NaCl and 10% loading buffer, 20% polyacrylamide gel with a 10% loading gel, 1 h 40 min, 4 °C, 170 V, 6 mA, 2 W. Left lane: DNA ladder.

Similar articles

Cited by

References

    1. Hunter C A, Sanders J K M. J Am Chem Soc. 1990;112:5525–5534. doi: 10.1021/ja00170a016. - DOI
    1. Hunter C A, Lawson K R, Perkins J, Urch C J. J Chem Soc, Perkin Trans 2. 2001:651–669. doi: 10.1039/b008495f. - DOI
    1. Salonen L M, Ellermann M, Diederich F. Angew Chem, Int Ed. 2011;50:4808–4842. doi: 10.1002/anie.201007560. - DOI - PubMed
    1. Grimme S. Angew Chem, Int Ed. 2008;47:3430–3434. doi: 10.1002/anie.200705157. - DOI - PubMed
    1. Martinez C R, Iverson B L. Chem Sci. 2012;3:2191–2201. doi: 10.1039/c2sc20045g. - DOI

LinkOut - more resources