4.8 Article

Catalytic Nanoassemblies Formed by Short Peptides Promote Highly Enantioselective Transfer Hydrogenation

Journal

ACS NANO
Volume 13, Issue 8, Pages 9292-9297

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b03880

Keywords

peptide; catalysis; self-assembly; micelle; vesicle; ATH; enantioselective

Funding

  1. NIH [GM119634]
  2. CRDF [OISE-18-63891-0]
  3. Ralph E. Powe Junior Enhancement Award
  4. Nappi Family Award
  5. Alexander von Humboldt Foundation

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Self-assembly enables formation of incredibly diverse supramolecular structures with practically important functions from simple and inexpensive building blocks. Here, we show how a semirational, bottom-up approach to create emerging properties can be extended to a design of highly enantioselective catalytic nanoassemblies. The designed peptides comprising as few as two amino acid residues spontaneously self-assemble in the presence of metal ions to form supramolecular, vesicle-like nanoassemblies that promote transfer hydrogenation of ketones in an aqueous phase with excellent conversion rates and enantioselectivities (>90% ee).

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