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Aleksandar Jeremic Department of Biological Sciences The George Washington University

Molecular Mechanism of Insulin and Amylin Release in the b -cell and Etiology of Type II Diabetes Mellitus. Aleksandar Jeremic Department of Biological Sciences The George Washington University Phone: (202) 994-7899 Email: jerema@gwu.edu http://www.gwu.edu/%7Eclade/faculty/jeremic /.

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Aleksandar Jeremic Department of Biological Sciences The George Washington University

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  1. Molecular Mechanism of Insulin and Amylin Release in the b-cell and Etiology of Type II Diabetes Mellitus Aleksandar Jeremic Department of Biological Sciences The George Washington University Phone: (202) 994-7899 Email: jerema@gwu.edu http://www.gwu.edu/%7Eclade/faculty/jeremic/

  2. 2D / 3D AFM image of amylin fibril growth insulin amylin Overall Goal: To dissect the “nanomechaniscs” of the insulin and amylin release in the b-cell and etiology of TTDM

  3. Research Aims Aim 1.Unraveling machinery regulating insulin and amylin release in b-cells: A. Role of intracellular water channels and heterotrimeric G-proteins B. Role of GTP-ase dynamin and actin Aim 2.Molecular mechanism of amylin –derived islet amyloidosis: A. Role of chaperones B. Role of metal (Zn)-peptide complexes

  4. Aim 1. Nanoscale Imaging of Hormone Secretion and Membrane Dynamics in the b-cell Approach: -Combined AFM and Confocal imaging Phogrin NPY Secretory vesicle NPY-RFP (cargo) Phogrin-GFP (membrane)

  5. Role of intracellular water channels and heterotrimeric G-proteins in regulation of insulin release Role of dynamin and actin in the fusion pore dynamics and vesicle recycling in the b-cell Approach: -AFM, Confocal, ELISA - RNA interference - Inhibitors (cytoch. D) Approach: -AFM, Confocal Microscopy, ELISA -Blockers (Hg; Ab) -AQPs (RNA interference)

  6. Aim 2. Molecular mechanism of islet amyloidosis 18 23 25 29 hAmylin: KCNTATCATQRLANFLVHSSNNFGAILSSTNVGSNTY rAmylin: KCNTATCATQRLANFLVRSSNNLGPVLPPTNVGSNTY insulin b-cell amylin (MIN-6) amyloid fibrils Approach: -Dynamics of amyloid fibril assembly (time-lapse AFM) -Dysfunction of insulin release (TIRF and ELISA) -Cell integrity (Ca2+ imaging, Caspases activation) -Peptide conformation transitions (CD and Raman Spectroscopy) -Protein-Lipid interactions (AFM-Force Imaging; microcalorimetry)

  7. Role of chaperones in amylin processing and fibrilogenesis Role of metal-peptide complexes in islet amyloid fibril formation Zn 7B2 Chaperone insulin amylin PC2 pre-pro-amylin amylin • Approach: • - RNA interference • Over expression of its dominant • negative form • Approach: • - AFM, CD, ITC • Single aa substitution: • 1. His18 (Zn-peptide complex) • 2. Phe23 (aromatic interactions) • 3. Pro25-29 (secondary structure)

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