Engineering disease analyte response in peptide self-assembly.

J Mater Chem B

Department of Chemical & Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556, USA.

Published: October 2024

AI Article Synopsis

  • * Self-assembled peptides are highlighted as an effective platform for creating nanoscale materials that can adapt to various disease-related signals like pH changes and glucose levels.
  • * The review discusses how engineering peptide sequences and adding non-peptidic elements can enable these nanocarriers to respond to specific small molecules associated with diseases.

Article Abstract

A need to enhance the precision and specificity of therapeutic nanocarriers inspires the development of advanced nanomaterials capable of sensing and responding to disease-related cues. Self-assembled peptides offer a promising nanocarrier platform with versatile use to create precisely defined nanoscale materials. Disease-relevant cues can range from large biomolecules, such as enzymes, to ubiquitous small molecules with varying concentrations in healthy diseased states. Notably, pH changes (, H concentration), redox species (, HO), and glucose levels are significant spatial and/or temporal indicators of therapeutic need. Self-assembled peptides respond to these cues by altering their solubility, modulating electrostatic interactions, or facilitating chemical transformations through dynamic or labile bonds. This review explores the design and construction of therapeutic nanocarriers using self-assembled peptides, focusing on how peptide sequence engineering along with the inclusion of non-peptidic components can link the assembly state of these nanocarriers to the presence of disease-relevant small molecules.

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Source
http://dx.doi.org/10.1039/d4tb01860eDOI Listing

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