Cross‐Binding of Adenosine by Aptamers Selected Using Theophylline

Abstract: We recently reported that some adenosine binding aptamers can also bind caffeine and theophylline with around 20‐fold lower affinities. This discovery led to the current work to examine the cross‐binding of adenosine to theophylline aptamers. For the DNA aptamer for theophylline, cross‐binding to adenosine was observed, and the affinity was 18 to 38‐fold lower for adenosine based on assays using isothermal titration calorimetry and ThT fluorescence spectroscopy. The binding complexes were characterized using NMR spectroscopy, and both adenosine and theophylline showed an overall similar binding structure to the DNA theophylline aptamer, although small differences were also observed. In contrast, the RNA aptamer did not show binding to adenosine, although both aptamers have very similar relative selectivity for various methylxanthines including caffeine. After a negative selection, a few new aptamers with completely different primary sequences for theophylline were obtained and they did not show binding to adenosine. Thus, there are many ways for aptamers to bind theophylline and some can have cross‐binding to adenosine. In biology, theophylline, caffeine, and adenosine can bind to the same protein receptors to regulate sleep, and their binding to the same DNA motifs may suggest an early role of nucleic acids in similar regulatory functions.

Object Details

• Location: Deutsche Nationalbibliothek Frankfurt am Main
• Extent: Online-Ressource
• Language: Englisch

References and Relationships

• Bibliographic citation: Cross‐Binding of Adenosine by Aptamers Selected Using Theophylline ; day:12 ; month:10 ; year:2023 ; extent:9 ; ChemBioChem ; (12.10.2023) (gesamt 9)

Contributors, Places and Time

• Creator: Huang, Po‐Jung Jimmy ; Evans, Natasha M. ; Lu, Chang ; Li, Albert Zehan ; Dieckmann, Thorsten ; Liu, Juewen

Further information

• DOI: 10.1002/cbic.202300566
• URN: urn:nbn:de:101:1-2023101215315207427986
• Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Last update: 14.08.2025, 10:58 AM CEST