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Controlling macromolecular conformation for the nanoscale transmission of information

Le Bailly, Bryden

[Thesis]. Manchester, UK: The University of Manchester; 2015.

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Abstract

Helical oligomers made up of the achiral amino acid Aib (2-aminoisobutyric acid) have great potential in relaying stereochemical information over nanometre distances by control of their macromolecular conformation. In a synthetic signalling pathway, the helical domain acts as a transducer, mediating the information flow between an input and an output. This thesis describes the advancement of these helical systems into functioning, dynamic transduction pathways capable of nanoscale information processing by a variety of different means.Through studying the effect of C-terminal chiral amino acids, alanine was found to give maximal control over the helical screw-sense. It was also discovered that the hydrogen bonding preference of the terminal group (ester, amide etc.) determined the screw-sense direction. By modifying the terminus, this directional preference was inverted using light or pH as secondary stimuli.Non-covalent interactions with solvent were found to be important in controlling the flow of information through the helical domain. In less polar solvents (THF, chloroform) a single screw sense can prevail for up to 200 monomers, leading to very low signal loss.A zinc binding site was developed to allow a chiral ligand to act as the input in the signalling process. Both amino and phosphoric acids led to remarkable levels of screw-sense induction. Using the reversible ligand binding interaction a pH switch was set up to moderate the binding of these two ligands, creating a ternary information switch. Significant progress was also made towards a light switch using a spiropyran as a competing ligand.Finally, a novel light-responsive switch capable of releasing a signalling molecule in solution was conceived and developed.

Bibliographic metadata

Type of resource:
Content type:
Form of thesis:
Type of submission:
Degree type:
Doctor of Philosophy
Degree programme:
PhD Chemistry (42 month)
Publication date:
Location:
Manchester, UK
Total pages:
278
Abstract:
Helical oligomers made up of the achiral amino acid Aib (2-aminoisobutyric acid) have great potential in relaying stereochemical information over nanometre distances by control of their macromolecular conformation. In a synthetic signalling pathway, the helical domain acts as a transducer, mediating the information flow between an input and an output. This thesis describes the advancement of these helical systems into functioning, dynamic transduction pathways capable of nanoscale information processing by a variety of different means.Through studying the effect of C-terminal chiral amino acids, alanine was found to give maximal control over the helical screw-sense. It was also discovered that the hydrogen bonding preference of the terminal group (ester, amide etc.) determined the screw-sense direction. By modifying the terminus, this directional preference was inverted using light or pH as secondary stimuli.Non-covalent interactions with solvent were found to be important in controlling the flow of information through the helical domain. In less polar solvents (THF, chloroform) a single screw sense can prevail for up to 200 monomers, leading to very low signal loss.A zinc binding site was developed to allow a chiral ligand to act as the input in the signalling process. Both amino and phosphoric acids led to remarkable levels of screw-sense induction. Using the reversible ligand binding interaction a pH switch was set up to moderate the binding of these two ligands, creating a ternary information switch. Significant progress was also made towards a light switch using a spiropyran as a competing ligand.Finally, a novel light-responsive switch capable of releasing a signalling molecule in solution was conceived and developed.
Thesis main supervisor(s):
Language:
en

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:266282
Created by:
Le Bailly, Bryden
Created:
10th June, 2015, 15:47:28
Last modified by:
Le Bailly, Bryden
Last modified:
9th September, 2016, 13:01:17

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