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d-Amino Acids and d-Foldamers : New helical constructs for catalysis

Lead Research Organisation: King's College London
Department Name: Chemistry

Abstract

The synthesis of 3 main delta-amino acid target molecules, and their related analogous, leading to the generation of a library of diverse monomers. From this, simple a,d- peptide sequences will then be synthesised, with a view to eventually synthesising rationally designed, novel aldolase peptide sequences.

A variety of conventional organic synthetic techniques are to be used in the synthesis of the amino acid target molecules, with organocatalysis being a common theme.
Solution phase synthesis used in order to synthesis the desired peptide sequences.
Use of NMR, CD and X-ray crystallography to gain structural information for the peptides.

Publications

10 25 50

Studentship Projects

Project Reference Relationship Related To Start End Student Name
EP/N509498/1 30/09/2016 29/09/2021
1951102 Studentship EP/N509498/1 30/09/2017 14/06/2022 Ryan Stendall
EP/R513064/1 30/09/2018 29/09/2023
1951102 Studentship EP/R513064/1 30/09/2017 14/06/2022 Ryan Stendall
 
Description The synthesis of novel amino acids and their incorporation into small peptides, diversifying the pool of monomers that could be used to create new enzyme-mimicking structures.
Exploitation Route Using these novel amino acid building blocks, new catalysts and enzyme-like molecules could be created, allowing for the more efficient and versatile synthesis of small molecules in industry (pharma, specialist chemicals, etc).

Potential for medicinal applications, ie. antibacterial peptides.
Sectors Chemicals

Manufacturing

including Industrial Biotechology

Pharmaceuticals and Medical Biotechnology