Aldehyde and CyClick Cyclization Impacts on Peptide Cellular Permeability Público
Pineda, Eddy (Spring 2023)
Abstract
Peptides and other hydrophobic molecules are considered viable candidates for drug discovery and biotherapeutic development due to their high affinity and specificity, but they suffer from poor cell penetration and stability. One potential solution to these issues has been the cyclization of peptides, but they also suffer from poor cellular permeability. A cyclization method known as CyClick has been developed in recent years that seek to overcome these issues. This method results in forming a 4-imidazolidinone moiety which introduces a ring to the peptide. A peptide’s ability to permeate the cell is due to varying structural motifs or conformations such as cyclization or the presence of certain functional groups. This study seeks to determine the effect of 4-imidazolidinone and aldehydes on peptide cell permeability. A series of cyclic peptides, peptide aldehydes, and CyClick peptides were synthesized and tagged with a chloroalkane tag to examine permeability. Using a recently developed chloroalkane penetration assay (CAPA), the permeability of these peptides was examined in cell models. The presence of both 4-imidazolidinone and aldehydes increased the permeability of peptides compared to cyclic and linear peptides not containing these structures. Further studies are being done to examine the impact of multiple aldehydes and their presence on cyclic peptides on cellular permeability. If these structures increase cellular permeability at a comparable rate to other permeability methods, then peptides aldehydes and CyClick-made aldehydes can be explored for future use in therapeutics and drug development.
Table of Contents
Table of Contents
Chapter 1: Introduction
Peptides as Drug Candidates
CyClick Chemistry and Purpose
Chapter 2: Materials and Methods
Synthesis of Linear Peptides
Synthesis of Fmoc-Alanine-Aldehyde
Synthesis of Aldehyde Resin
Synthesis of Aldehyde Linear Peptides
Synthesis of Macrocyclic Peptides
Synthesis of CyClick Peptides
Synthesis of Aldehyde Macrocyclic Peptides
Synthesis of Chloroalkane Tag
Deprotection of O-Allyl Glutamic Acid Containing Peptides
Coupling of Chloroalkane Tag and Peptide
Chloroalkane Penetration Assay
Chapter 3: Results and Discussion
Chapter 4: Conclusions and Future Directions
References
Supplemental Information
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