4.5 Article

Attachment of cyclodextrin acids to PEGA resin and study of binding with fluorescence microscopy

Journal

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 43, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2021.128060

Keywords

Molecular recognition; Purification; Supramolecar interaction; Solid phase

Funding

  1. Danish Hydrocarbon Research and Technology Centre (DHRTC)

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Three different cyclodextrin acids were attached to amino PEGA resin as amides and studied for their host-guest binding with ANS. The binding characteristics and dissociation constants were determined, showing selective inhibition by specific guest molecules for certain cyclodextrin acids.
Three different cyclodextrin acids, 6A,6D-di-O-(prop-2-carboxy-1,3-dienyl)-alpha-cyclodextrin (1), 6-deoxy-beta-cyclodextrin-6-carboxylic acid (2), 6-deoxy-beta-cyclodextrin-6-ethylenecarboxylic acid (3), were prepared and attached to amino PEGA resin as amides using coupling conditions with COMU and NEM. Host-guest binding to the resins was studied by fluorescence microscopy using 8-anilinoaphtalene-1-sulfonic acid (ANS) as guest, and was found to follow the equation IF = IFmax*[ANS]/([ANS] + Kd) where F, Fmax and Kd are the fluorescence, maximum fluorescence and Kd the dissociation constant for the ANS-cyclodextrin complex, respectively. Kd was 4.4, 2.4 and 4.9 x 10-4 M for the three resins. Competitive inhibition of ANS binding was performed with 1-adamantanylamine and octyl beta-D-glucoside with the latter being selective for the alpha-cyclodextrin as expected.

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