Ligand-Controlled Assembly of Hexamers, Dihexamers, and Linear Multihexamer Structures by the Engineered Acylated Insulin Degludec

• Published in: Biochemistry (Easton) 2013-01, Vol.52 (2), p.295-309
• Main Authors: Steensgaard, Dorte B, Schluckebier, Gerd, Strauss, Holger M, Norrman, Mathias, Thomsen, Jens K, Friderichsen, Anders V, Havelund, Svend, Jonassen, Ib
• Format: Article
• Language: English
• Subjects: Acetylation; Amino Acid Sequence; Circular Dichroism; Crystallography, X-Ray; Humans; Insulin, Long-Acting - chemistry; Insulin, Long-Acting - metabolism; Ligands; Models, Molecular; Molecular Sequence Data; Phenol - metabolism; Protein Binding; Protein Conformation; Protein Multimerization; Resorcinols - metabolism; Scattering, Small Angle; Ultracentrifugation; X-Ray Diffraction; Zinc - metabolism
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi3008609

Insulin degludec, an engineered acylated insulin, was recently reported to form a soluble depot after subcutaneous injection with a subsequent slow release of insulin and an ultralong glucose-lowering effect in excess of 40 h in humans. We describe the structure, ligand binding properties, and self-assemblies of insulin degludec using orthogonal structural methods. The protein fold adopted by insulin degludec is very similar to that of human insulin. Hexamers in the R6 state similar to those of human insulin are observed for insulin degludec in the presence of zinc and resorcinol. However, under conditions comparable to the pharmaceutical formulation comprising zinc and phenol, insulin degludec forms finite dihexamers that are composed of hexamers in the T3R3 state that interact to form an R3T3–T3R3 structure. When the phenolic ligand is depleted and the solvent condition thereby mimics that of the injection site, the quaternary structure changes from dihexamers to a supramolecular structure composed of linear arrays of hundreds of hexamers in the T6 state and an average molar mass, M 0, of 59.7 × 103 kg/mol. This novel concept of self-assemblies of insulin controlled by zinc and phenol provides the basis for the slow action profile of insulin degludec. To the best of our knowledge, this report for the first time describes a tight linkage between quaternary insulin structures of hexamers, dihexamers, and multihexamers and their allosteric state and its origin in the inherent propensity of the insulin hexamer for allosteric half-site reactivity.