Fish-hunting cone snail venoms are a rich source of minimized ligands of the vertebrate insulin receptor
Peter Ahorukomeye,
Maria M Disotuar,
Joanna Gajewiak,
Santhosh Karanth,
Maren Watkins,
Samuel D Robinson,
Paula Flórez Salcedo,
Nicholas A Smith,
Brian J Smith,
Amnon Schlegel,
Briony E Forbes,
Baldomero Olivera,
Danny Hung-Chieh Chou,
Helena Safavi-Hemami
Affiliations
Peter Ahorukomeye
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States
Maria M Disotuar
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States
Joanna Gajewiak
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States
Santhosh Karanth
Molecular Medicine Program, University of Utah, Salt Lake City, United States; Department of Internal Medicine, Division of Endocrinology, Metabolism and Diabetes, University of Utah School of Medicine, Salt Lake City, United States; Department of Nutrition and Integrative Physiology, College of Health, University of Utah, Salt Lake City, United States
Maren Watkins
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States
Samuel D Robinson
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States
Paula Flórez Salcedo
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States
Nicholas A Smith
La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Australia
Brian J Smith
La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Australia
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States; Molecular Medicine Program, University of Utah, Salt Lake City, United States; Department of Internal Medicine, Division of Endocrinology, Metabolism and Diabetes, University of Utah School of Medicine, Salt Lake City, United States; Department of Nutrition and Integrative Physiology, College of Health, University of Utah, Salt Lake City, United States
Briony E Forbes
Department of Medical Biochemistry, Flinders University, Bedford Park, Australia
Baldomero Olivera
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States
Danny Hung-Chieh Chou
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States
Department of Biology, University of Utah School of Medicine, Salt Lake City, United States; Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States
The fish-hunting marine cone snail Conus geographus uses a specialized venom insulin to induce hypoglycemic shock in its prey. We recently showed that this venom insulin, Con-Ins G1, has unique characteristics relevant to the design of new insulin therapeutics. Here, we show that fish-hunting cone snails provide a rich source of minimized ligands of the vertebrate insulin receptor. Insulins from C. geographus, Conus tulipa and Conus kinoshitai exhibit diverse sequences, yet all bind to and activate the human insulin receptor. Molecular dynamics reveal unique modes of action that are distinct from any other insulins known in nature. When tested in zebrafish and mice, venom insulins significantly lower blood glucose in the streptozotocin-induced model of diabetes. Our findings suggest that cone snails have evolved diverse strategies to activate the vertebrate insulin receptor and provide unique insight into the design of novel drugs for the treatment of diabetes.