作者
Thomas Høeg-Jensen,Rita Slaaby,Thomas Kruse,Christian L. Brand,Jeppe Sturis,Christian Fledelius,P.A. Nielsen,Erica Nishimura,Alice R. Madsen,Lennart Lykke,Kim Halskov,Simona Koščová,Vladaslav Kotek,Anthony P. Davis,Robert A. Tromans,Michael Tomsett,Guillem Peñuelas-Haro,Daniel J. Leonard,Michael J. Orchard,Andy Chapman,Gaetano Invernizzi,Eva Johansson,Daniele Granata,Bo T. Hansen,Thomas Garm Pedersen,Jonas Kildegaard,Karen M. Pedersen,Hanne H. F. Refsgaard,Lene Alirangis,Johannes Josef Fels,A.V. Neutzsky-Wulff,Per Sauerberg
摘要
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 blood glucose values within normal range, but matching insulin doses to fluctuating glucose levels is difficult since 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 thus 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 glucose over the physiological range 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 of NNC2215 increased 12-fold when glucose concentration was increased from 0 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.