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Detalle de: A novel amyloid designable scaffold and potential inhibitor inspired by GAIIG of amyloid beta and the HIV‐1 V3 loop

Title A novel amyloid designable scaffold and potential inhibitor inspired by GAIIG of amyloid beta and the HIV‐1 V3 loop
Abstract

The GAIIG sequence, common to the amyloid beta peptide (residues 29–33) and to the HIV ‐1 gp120 (residues 24–28 in a typical V3 loop), self‐assembles into amyloid fibrils, as suggested by theory and the experiments presented here. The longer YATGAIIGNII sequence from the V3 loop also self‐assembles into amyloid fibrils, of which the first three and the last two residues are outside the amyloid GAIIG core. We postulate that this sequence, with suitably selected modifications at the flexible positions, can serve as a designable scaffold for novel amyloid‐based materials. Moreover, we report the single crystal X‐ray structure of the beta‐breaker peptide GAIPIG at 1.05 Å resolution. The structural information provided in this study could serve as the basis for structure‐based design of potential inhibitors of amyloid formation.

Apa Reference Kokotidou, C., Jonnalagadda, S. V. R., Orr, A. A., Seoane‐Blanco, M., Apostolidou, C. P., van Raaij, M. J., Kotzabasaki, M., Chatzoudis, A., Jakubowski, J. M., Mossou, E., Forsyth, V. T., Mitchell, E. P., Bowler, M. W., Llamas‐Saiz, A. L., Tamamis, P., & Mitraki, A. (2018). A novel amyloid designable scaffold and potential inhibitor inspired by <scp>GAIIG</scp> of amyloid beta and the <scp>HIV</scp>‐1 V3 loop. FEBS Letters, 592(11), 1777–1788. Portico. 10.1002/1873-3468.13096
Doi 10.1002/1873-3468.13096
Publication Date Jun 2018
Publication Type Article
Researcher Mark van Raaij
Ontology Genome Assembly, Drug Discovery and design
Research Groups Structural Biology of Virus Proteins
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