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. Author manuscript; available in PMC: 2012 Sep 28.
Published in final edited form as: J Am Chem Soc. 2011 Sep 7;133(38):14975–14977. doi: 10.1021/ja206742m

Figure 1.

Figure 1

(A) Assembly mechanisms for enantiomeric peptides leading to the formation of a fibrillar network that defines hydrogelation. Enantiomers can either self-sort to form fibrils that are homogeneous with respect to enantiomer (solid colored fibrils) or enantiomers can co-assemble to form a network of fibrils that are heterogeneous with respect to enantiomer (multi-colored fibrils). (B) Sequences of enantiomers MAX1, DMAX1 and the non-isomeric Control Peptide. D-amino acid residues are italicized.