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Updated: Jun 27, 2025

Microfluidic Mixers for Studying Protein Folding
Published on: April 10, 2012
Domain Swapping in Abiotic Foldamers
Shuhe Wang1, Barbara Wicher2, Céline Douat1
1Department of Pharmacy, Ludwig-Maximilians-Universität in Munich, Butenandtstr. 5-13, 81377, München, Germany.
Abstract:
Foldamer sequences that adopt tertiary helix-turn-helix folds mediated by helix-helix hydrogen bonding in organic solvents have been previously reported. In an attempt to create genuine abiotic quaternary structures, i.e. assemblies of tertiary structures, new sequences were prepared that possess additional hydrogen bond donors at positions that may promote an association between the tertiary folds. However, a solid state structure and extensive solution state investigations by Nuclear Magnetic Resonance (NMR) and Circular Dichroism (CD) show that, instead of forming a quaternary structure, the tertiary folds assemble into stable domain-swapped dimer motifs. Domain swapping entails a complete reorganization of the arrays of hydrogen bonds and changes in relative helix orientation and handedness that can all be rationalized.
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