Optimising the SICLOPPS-RTHS screening methodology to identify more potent cyclic peptide inhibitors of IDOL
Optimising the SICLOPPS-RTHS screening methodology to identify more potent cyclic peptide inhibitors of IDOL
Circulating cholesterol is removed from blood plasma by cellular uptake via the low density lipoprotein receptor (LDLR). The inducible degrader of the LDLR (IDOL) is a post-translational regulator of the LDLR. IDOL homodimerization is essential for IDOL mediated degradation of the LDLR. Previous research utilised a genetic screening platform to screen for inhibitors of the IDOL homodimer PPI and identified cyclo-CFFLYT as an inhibitor of IDOL homodimerization. The affinity of the inhibitor was improved by incorporating non-natural phenylalanine analogues in place of the second phenylalanine, leading to the identification of cyclo-CF-Cha-LYT. This work aimed to investigate the structure-activity relationship of cyclo-CF-Cha-LYT and to optimise the SICLOPPS-RTHS (split-intein circular ligation of peptides and proteins - reverse twohybrid system) screening set-up to identify further inhibitors of IDOL. An alanine scan was performed by MST using Cy5 labelled YPet-IDOL, which identified cysteine and 3-cyclohexyl-Lalanine as critical residues of cyclo-CF-Cha-LYT. Chemically similar derivatives of cysteine were tested to investigate the interaction between the cysteine residue and IDOL. Only sulfurcontaining residues bound to IDOL which indicated that the residue was likely involved in a sulfurpi interaction, after eliminating disulfides and hydrogen bonding as possible interactions. CycloCF-Cha-LYT was not pursued any further due to a poor aqueous solubility, poor selectivity and a high clogP of 6.03. The SICLOPPS-RTHS screening set-up was adapted to be compatible with next-generation sequencing technologies. A screen was performed with the updated set-up and a CX5 SICLOPPS library, which identified two single-digit micromolar inhibitors of the IDOL homodimer, among other less active hits. The NGS screen was shown to be a success, as the hits obtained were more active and greater in number than those found in the traditional screen of the IDOL RTHS.
University of Southampton
Craswell, James Anthony
7b33adf1-723e-44bf-8bb6-1134e1114d1f
2023
Craswell, James Anthony
7b33adf1-723e-44bf-8bb6-1134e1114d1f
Tavassoli, Ali
d561cf8f-2669-46b5-b6e1-2016c85d63b2
Craswell, James Anthony
(2023)
Optimising the SICLOPPS-RTHS screening methodology to identify more potent cyclic peptide inhibitors of IDOL.
University of Southampton, Doctoral Thesis, 186pp.
Record type:
Thesis
(Doctoral)
Abstract
Circulating cholesterol is removed from blood plasma by cellular uptake via the low density lipoprotein receptor (LDLR). The inducible degrader of the LDLR (IDOL) is a post-translational regulator of the LDLR. IDOL homodimerization is essential for IDOL mediated degradation of the LDLR. Previous research utilised a genetic screening platform to screen for inhibitors of the IDOL homodimer PPI and identified cyclo-CFFLYT as an inhibitor of IDOL homodimerization. The affinity of the inhibitor was improved by incorporating non-natural phenylalanine analogues in place of the second phenylalanine, leading to the identification of cyclo-CF-Cha-LYT. This work aimed to investigate the structure-activity relationship of cyclo-CF-Cha-LYT and to optimise the SICLOPPS-RTHS (split-intein circular ligation of peptides and proteins - reverse twohybrid system) screening set-up to identify further inhibitors of IDOL. An alanine scan was performed by MST using Cy5 labelled YPet-IDOL, which identified cysteine and 3-cyclohexyl-Lalanine as critical residues of cyclo-CF-Cha-LYT. Chemically similar derivatives of cysteine were tested to investigate the interaction between the cysteine residue and IDOL. Only sulfurcontaining residues bound to IDOL which indicated that the residue was likely involved in a sulfurpi interaction, after eliminating disulfides and hydrogen bonding as possible interactions. CycloCF-Cha-LYT was not pursued any further due to a poor aqueous solubility, poor selectivity and a high clogP of 6.03. The SICLOPPS-RTHS screening set-up was adapted to be compatible with next-generation sequencing technologies. A screen was performed with the updated set-up and a CX5 SICLOPPS library, which identified two single-digit micromolar inhibitors of the IDOL homodimer, among other less active hits. The NGS screen was shown to be a success, as the hits obtained were more active and greater in number than those found in the traditional screen of the IDOL RTHS.
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Submitted date: 11 December 2022
Published date: 2023
Identifiers
Local EPrints ID: 472675
URI: http://eprints.soton.ac.uk/id/eprint/472675
PURE UUID: edc6315e-4e07-460a-a000-5b487378ac12
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Date deposited: 14 Dec 2022 17:30
Last modified: 17 Mar 2024 03:07
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Author:
James Anthony Craswell
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