The effect of l-thymidine, acyclic thymine and 8-bromoguanine on the stability of model G-quadruplex structures

Biochim Biophys Acta Gen Subj. 2017 May;1861(5 Pt B):1205-1212. doi: 10.1016/j.bbagen.2016.09.030. Epub 2016 Oct 2.

Abstract

Background: Guanine-rich oligonucleotides are capable of forming tetrahelical structures known as G-quadruplexes with interesting biological properties. We have investigated the effects of site-specific substitution in the loops and in the tetrads model G-quadruplexes using thymine glycol nucleic acid (GNA) units, l-thymidine and 8-Br-2'-deoxyguanosine.

Methods: Modified oligonucleotides were chemically synthesized and spectroscopic techniques were used to determine the relative stability of the modified G-quadruplex. The double 8-BrdG-modified quadruplexes were further characterized by Nuclear Magnetic Resonance. Binding to thrombin of selected quadruplex was analyzed by gel electrophoresis retention assay.

Results: The most interesting results were found with a 8-bromoG substitution that had the larger stabilization of the quadruplex. NMR studies indicate a tight relationship between the loops and the tetrads to accommodate 8-bromoG modifications within the TBA.

Conclusions: The substitutions of loop positions with GNA T affect the TBA stability except for single modification in T7 position. Single l-thymidine substitutions produced destabilization of TBA. Larger changes on quadruplex stability are observed with the use of 8-bromoG finding a single substitution with the highest thermal stabilization found in thrombin binding aptamers modified at the guanine residues and having good affinity for thrombin. Double 8-BrdG modification in anti positions of different tetrads produce a conformational flip from syn to anti conformation of 8-Br-dG to favor loop-tetrad interaction and preserve the overall TBA stability.

General significance: Modified guanine-rich oligonucleotides are valuable tools for the search for G-quadruplex structures with higher thermal stability and may provide compounds with interesting protein-nucleic acid binding properties. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.

Keywords: 8-bromo-2′-deoxyguanine; G-quadruplex; NMR; Thrombin binding aptamer; Thymine glycol nucleic acid; l-thymidine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Deoxyadenosines / chemistry*
  • Deoxyadenosines / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • G-Quadruplexes*
  • Guanine / analogs & derivatives*
  • Guanine / chemistry
  • Guanine / metabolism
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Oligonucleotides / chemistry*
  • Oligonucleotides / metabolism
  • Protein Binding
  • Structure-Activity Relationship
  • Thrombin / chemistry
  • Thrombin / metabolism
  • Thymidine / chemistry*
  • Thymidine / metabolism

Substances

  • 8-bromoguanine
  • Deoxyadenosines
  • Oligonucleotides
  • 8-bromo-2'-deoxyadenosine
  • Guanine
  • Thrombin
  • Thymidine