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Updated: Jun 12, 2026

Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability
Published on: April 2, 2015
Attractive interactions between side chains of histidine-histidine and histidine-arginine-based cationic dipeptides
Jan Heyda1, Philip E Mason, Pavel Jungwirth
1Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 16610 Prague 6, Czech Republic.
Abstract:
Molecular dynamics simulations of histidine-based dipeptides in water show that a protonated histidine side chain group has a propensity for forming like-charged contact pairs with another protonated histidine or with arginine. This effect is of similar strength to that in previously observed arginine-arginine pairing. Even stronger contact pairs are formed in singly protonated or deprotonated dihistidine, where stacking of aromatic rings is not weakened by Coulomb repulsion between the side chains. Similar pairing behavior is also observed in a mixed solution of imidazole and imidazolium chloride.
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