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
{"title":"对葡萄糖敏感的胰岛素,可减轻低血糖症状","authors":"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","doi":"10.1038/s41586-024-08042-3","DOIUrl":null,"url":null,"abstract":"The risk of inducing hypoglycaemia (low blood glucose) constitutes the main challenge associated with insulin therapy for diabetes1,2. 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 hypoglycaemia3. 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 macrocycle4 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. 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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 macrocycle4 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. 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Glucose-sensitive insulin with attenuation of hypoglycaemia
The risk of inducing hypoglycaemia (low blood glucose) constitutes the main challenge associated with insulin therapy for diabetes1,2. 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 hypoglycaemia3. 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 macrocycle4 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. NNC2215 is an insulin conjugate that can reversibly adjust its bioactivity in response to a diabetes-relevant glucose range in vivo.
期刊介绍:
Nature is a prestigious international journal that publishes peer-reviewed research in various scientific and technological fields. The selection of articles is based on criteria such as originality, importance, interdisciplinary relevance, timeliness, accessibility, elegance, and surprising conclusions. In addition to showcasing significant scientific advances, Nature delivers rapid, authoritative, insightful news, and interpretation of current and upcoming trends impacting science, scientists, and the broader public. The journal serves a dual purpose: firstly, to promptly share noteworthy scientific advances and foster discussions among scientists, and secondly, to ensure the swift dissemination of scientific results globally, emphasizing their significance for knowledge, culture, and daily life.