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Mol Pharm ; 18(9): 3272-3280, 2021 09 06.
Article in English | MEDLINE | ID: mdl-34351780

ABSTRACT

Two different insulin analogues, insulin degludec and lithocholyl insulin, were studied by small-angle X-ray scattering with respect to their self-assembly and interactions in solution at different concentrations of insulin and salt, NaCl. Very different behavior was observed for the two. Insulin degludec, linked to a hexadecanedioic acid, consistently formed di-hexamers, without any further oligomeric growth upon screening of electrostatic repulsions, indicating a stable di-hexamer unit without further oligomerization, as expected in the presence of phenol. The other insulin analogue, linked to the sterol lithocholic acid, formed n-hexamers with n ranging from 1 to 15, increasing with NaCl concentration and insulin concentration, indicating attractive forces in competition with the electrostatic repulsion and solution entropy. At the highest concentration of insulin and NaCl, a liquid crystal phase was observed, which has not previously been identified, featuring a quadratic structure organized into layers, which might hold interesting properties for pharmaceutical applications.


Subject(s)
Insulin, Long-Acting/metabolism , Insulin/analogs & derivatives , Amino Acid Sequence , Chemistry, Pharmaceutical , Insulin/chemistry , Insulin/metabolism , Insulin, Long-Acting/chemistry , Models, Molecular , Protein Multimerization , Salinity , Scattering, Small Angle , X-Ray Diffraction
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