Binding Methylarginines and Methyllysines as Free Amino Acids: A Comparative Study of Multiple Host Classes. (24th November 2021)

• Record Type: Journal Article
• Authors: Warmerdam, Zoey; Kamba, Bianca E.; Le, My‐Hue; Schrader, Thomas; Isaacs, Lyle; Bayer, Peter; Hof, Fraser
• Is Part Of: Chembiochem. Volume 23:Number 2(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-11-24
• Subjects: host-guest chemistry -- indicator displacement assays -- macrocycles -- methylated amino acids; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pharmaceutical chemistry -- Periodicals; 572
• DOI: 10.1002/cbic.202100502
• Languages: English
• ISSNs: 1439-4227

Abstract

Abstract: Methylated free amino acids are an important class of targets for host‐guest chemistry that have recognition properties distinct from those of methylated peptides and proteins. We present comparative binding studies for three different host classes that are each studied with multiple methylated arginines and lysines to determine fundamental structure‐function relationships. The hosts studied are all anionic and include three calixarenes, two acyclic cucurbiturils, and two other cleft‐like hosts, a clip and a tweezer. We determined the binding association constants for a panel of methylated amino acids using indicator displacement assays. The acyclic cucurbiturils display stronger binding to the methylated amino acids, and some unique patterns of selectivity. The two other cleft‐like hosts follow two different trends, shallow host (clip) following similar trends to the calixarenes, and the other more closed host (tweezer) binding certain less‐methylated amino acids stronger than their methylated counterparts. Molecular modelling sheds some light on the different preferences of the various hosts. The results identify hosts with new selectivities and with affinities in a range that could be useful for biomedical applications. The overall selectivity patterns are explained by a common framework that considers the geometry, depth of binding pockets, and functional group participation across all host classes. Abstract : Comparative binding studies for three different host classes (calixarenes, acyclic cucurbiturils and other cleft‐like hosts) are presented. Each was studied with multiple methylated arginines and lysines to determine fundamental structure‐function relationships. Molecular modelling was used to gain insight on the preferences of the different hosts.