Fish-hunting cone snail venoms are a rich source of minimized ligands of the vertebrate insulin receptor

被引:49
作者
Ahorukomeye, Peter [1 ]
Disotuar, Maria M. [2 ]
Gajewiak, Joanna [1 ]
Karanth, Santhosh [3 ,4 ,5 ]
Watkins, Maren [1 ]
Robinson, Samuel D. [1 ]
Salcedo, Paula Florez [2 ]
Smith, Nicholas A. [6 ]
Smith, Brian J. [6 ]
Schlegel, Amnon [2 ,3 ,4 ,5 ]
Forbes, Briony E. [7 ]
Olivera, Baldomero [1 ]
Chou, Danny Hung-Chieh [2 ]
Safavi-Hemami, Helena [1 ,2 ]
机构
[1] Univ Utah, Sch Med, Dept Biol, Salt Lake City, UT 84132 USA
[2] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84132 USA
[3] Univ Utah, Mol Med Program, Salt Lake City, UT USA
[4] Univ Utah, Sch Med, Div Endocrinol Metab & Diabet, Dept Internal Med, Salt Lake City, UT USA
[5] Univ Utah, Coll Hlth, Dept Nutr & Integrat Physiol, Salt Lake City, UT USA
[6] La Trobe Univ, La Trobe Inst Mol Sci, Melbourne, Vic, Australia
[7] Flinders Univ S Australia, Dept Med Biochem, Bedford Pk, SA, Australia
来源
ELIFE | 2019年 / 8卷
关键词
BINDING; SUPERFAMILY; PEPTIDES; GENERATION; GEOGRAPHUS; EVOLUTION; BEHAVIOR; PLATFORM; BRAIN;
D O I
10.7554/eLife.41574
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:27
相关论文
共 52 条
[1]   Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers [J].
Abraham, Mark James ;
Murtola, Teemu ;
Schulz, Roland ;
Páll, Szilárd ;
Smith, Jeremy C. ;
Hess, Berk ;
Lindah, Erik .
SoftwareX, 2015, 1-2 :19-25
[2]   STRUCTURE OF RHOMBOHEDRAL 2 ZINC INSULIN CRYSTALS [J].
ADAMS, MJ ;
BLUNDELL, TL ;
DODSON, EJ ;
DODSON, GG ;
VIJAYAN, M ;
BAKER, EN ;
HARDING, MM ;
HODGKIN, DC ;
RIMMER, B ;
SHEAT, S .
NATURE, 1969, 224 (5218) :491-&
[3]   Evolution of the vertebrate insulin receptor substrate (Irs) gene family [J].
Al-Salam, Ahmad ;
Irwin, David M. .
BMC EVOLUTIONARY BIOLOGY, 2017, 17
[4]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[5]  
[Anonymous], CURR PROTOC BIOINFOR
[6]   Crystal structure of desheptapeptide(B24-B30)insulin at 1.6 angstrom resolution: Implications for receptor binding [J].
Bao, SJ ;
Xie, DL ;
Zhang, JP ;
Chang, WR ;
Liang, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :2975-2980
[7]   Optimization of the Additive CHARMM All-Atom Protein Force Field Targeting Improved Sampling of the Backbone φ, ψ and Side-Chain χ1 and χ2 Dihedral Angles [J].
Best, Robert B. ;
Zhu, Xiao ;
Shim, Jihyun ;
Lopes, Pedro E. M. ;
Mittal, Jeetain ;
Feig, Michael ;
MacKerell, Alexander D., Jr. .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2012, 8 (09) :3257-3273
[8]  
Blumenthal S, 2010, PERSPECT BIOL MED, V53, P491, DOI 10.1353/pbm.2010.0001
[9]  
Conlon JM, 2000, AM ZOOL, V40, P200
[10]  
CRUZ LJ, 1978, NAUTILUS, V92, P150