Islet amyloid-induced cell death and bilayer integrity loss share a molecular origin targetable with oligopyridylamide-based α-helical mimetics

Sunil Kumar, Diana E. Schlamadinger, Mark A. Brown, Joanna M. Dunn, Brandon Mercado, James A. Hebda, Ishu Saraogi, Elizabeth Rhoades, Andrew Hamilton, Andrew D. Miranker

Research output: Contribution to journalArticle

Abstract

Summary Islet amyloid polypeptide (IAPP) is a hormone cosecreted with insulin. IAPP proceeds through a series of conformational changes from random coil to β-sheet via transient α-helical intermediates. An unknown subset of these events are associated with seemingly disparate gains of function, including catalysis of self-assembly, membrane penetration, loss of membrane integrity, mitochondrial localization, and finally, cytotoxicity, a central component of diabetic pathology. A series of small molecule, α-helical mimetics, oligopyridylamides, was previously shown to target the membrane-bound α-helical oligomeric intermediates of IAPP. In this study, we develop an improved, microwave-assisted synthesis of oligopyridylamides. A series of designed tripyridylamides demonstrate that lipid-catalyzed self-assembly of IAPP can be deliberately targeted. In addition, these molecules affect IAPP-induced leakage of synthetic liposomes and cellular toxicity in insulin-secreting cells. The tripyridylamides inhibit these processes with identical rank orders of effectiveness. This indicates a common molecular basis for the disparate set of observed effects of IAPP.

Original languageEnglish (US)
Article number3006
Pages (from-to)369-378
Number of pages10
JournalChemistry and Biology
Volume22
Issue number3
DOIs
StatePublished - Mar 19 2015

Fingerprint

Islet Amyloid Polypeptide
Cell death
Amyloid
Cell Death
Membranes
Self assembly
Insulin
Molecules
Insulin-Secreting Cells
Mitochondrial Membranes
Pathology
Cytotoxicity
Microwaves
Catalysis
Liposomes
Toxicity
Hormones
Lipids

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Molecular Biology
  • Clinical Biochemistry
  • Molecular Medicine
  • Pharmacology

Cite this

Kumar, S., Schlamadinger, D. E., Brown, M. A., Dunn, J. M., Mercado, B., Hebda, J. A., ... Miranker, A. D. (2015). Islet amyloid-induced cell death and bilayer integrity loss share a molecular origin targetable with oligopyridylamide-based α-helical mimetics. Chemistry and Biology, 22(3), 369-378. [3006]. https://doi.org/10.1016/j.chembiol.2015.01.006

Islet amyloid-induced cell death and bilayer integrity loss share a molecular origin targetable with oligopyridylamide-based α-helical mimetics. / Kumar, Sunil; Schlamadinger, Diana E.; Brown, Mark A.; Dunn, Joanna M.; Mercado, Brandon; Hebda, James A.; Saraogi, Ishu; Rhoades, Elizabeth; Hamilton, Andrew; Miranker, Andrew D.

In: Chemistry and Biology, Vol. 22, No. 3, 3006, 19.03.2015, p. 369-378.

Research output: Contribution to journalArticle

Kumar, S, Schlamadinger, DE, Brown, MA, Dunn, JM, Mercado, B, Hebda, JA, Saraogi, I, Rhoades, E, Hamilton, A & Miranker, AD 2015, 'Islet amyloid-induced cell death and bilayer integrity loss share a molecular origin targetable with oligopyridylamide-based α-helical mimetics', Chemistry and Biology, vol. 22, no. 3, 3006, pp. 369-378. https://doi.org/10.1016/j.chembiol.2015.01.006
Kumar, Sunil ; Schlamadinger, Diana E. ; Brown, Mark A. ; Dunn, Joanna M. ; Mercado, Brandon ; Hebda, James A. ; Saraogi, Ishu ; Rhoades, Elizabeth ; Hamilton, Andrew ; Miranker, Andrew D. / Islet amyloid-induced cell death and bilayer integrity loss share a molecular origin targetable with oligopyridylamide-based α-helical mimetics. In: Chemistry and Biology. 2015 ; Vol. 22, No. 3. pp. 369-378.
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