Thomas Hoeg-Jensen, Thomas Kruse, Christian L. Brand, Jeppe Sturis, Christian Fledelius, Peter K. Nielsen, Erica Nishimura, Alice R. Madsen, Lennart Lykke, Kim S. Halskov, Simona Koščová, Vladislav Kotek, Anthony P. Davis, Robert A. Tromans, Michael Tomsett, Guillem Peñuelas-Haro, Daniel J. Leonard, Michael G. Orchard, Andy Chapman, Gaetano Invernizzi, Eva Johansson, Daniele Granata, Bo F. Hansen, Thomas A. Pedersen, Jonas Kildegaard, Karen-Margrethe Pedersen, Hanne H. F. Refsgaard, Lene Alifrangis, Johannes J. Fels, Anita V. Neutzsky-Wulff, Per Sauerberg & Rita Slaaby
Abstract
The risk of inducing hypoglycaemia (low blood glucose) constitutes the main challenge associated with insulin therapy for diabetes. Insulin doses must be adjusted to ensure that blood glucose values are within the normal range, but matching insulin doses to fluctuating glucose levels is difficult because even a slightly higher insulin dose than needed can lead to a hypoglycaemic incidence, which can be anything from uncomfortable to life-threatening. It has therefore been a long-standing goal to engineer a glucose-sensitive insulin that can auto-adjust its bioactivity in a reversible manner according to ambient glucose levels to ultimately achieve better glycaemic control while lowering the risk of hypoglycaemia. Here we report the design and properties of NNC2215, an insulin conjugate with bioactivity that is reversibly responsive to a glucose range relevant for diabetes, as demonstrated in vitro and in vivo. NNC2215 was engineered by conjugating a glucose-binding macrocycle and a glucoside to insulin, thereby introducing a switch that can open and close in response to glucose and thereby equilibrate insulin between active and less-active conformations. The insulin receptor affinity for NNC2215 increased 3.2-fold when the glucose concentration was increased from 3 to 20 mM. In animal studies, the glucose-sensitive bioactivity of NNC2215 was demonstrated to lead to protection against hypoglycaemia while partially covering glucose excursions.