Journal
BIOMACROMOLECULES
Volume 13, Issue 11, Pages 3562-3571Publisher
AMER CHEMICAL SOC
DOI: 10.1021/bm301007r
Keywords
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Funding
- National Institutes of Health [R21 HL102806]
- National Science Foundation Teragrid [MCB100057]
- National Science Foundation
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We hive investigated the self-assembly of fluorenylmethoxycarbonyl-conjugated dialanine (Fmoc-AA) molecules using combined computational and experimental approaches. Fmoc-AA gels Were Characterized using transmission electron microscopy (TM), circular dichroism (CD), Fourier transform infrared. (FTIR), and wide-angle X-ray scattering (WAXS). Computationally, we simulated the assembly of Fmoc-AA using molecular dynamics. techniques All simulations converged to a condensed fibril structure in which the Fmoc groups Stack mostly within in the center of the fibril. However, the Fmoc groups are partially exposed to water, creating an amphiphilic surface which may be responsible for the aggregation of fibrils into nanoscale fibers observed in TEM. From the fibril Models, radial distribution calculations agree with d-spacings observed in WAXS for the fibril diameter and pi-stacking interactions. Our analyses. Show that dialanine, despite its short length, adopts a mainly extended polyproline II conformation. In contrast to previous hypotheses, these results indicate that beta-sheet-like hydrogen bonding is not prevalent Rather, stacking of Fmoc groups, inter residue hydrogen bonding and hydrogen bonding with water play the important roles in stabilizing the fibril structure of supramolecular assemblies of short conjugated peptides.
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