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Evolution of branched peptides as novel biomaterials.

作者信息

Little Matthew J, Mason Jody M, Mehrban Nazia

机构信息

University of Bath, Claverton Down, Bath, BA2 7AY, UK.

出版信息

J Mater Chem B. 2025 Feb 12;13(7):2226-2241. doi: 10.1039/d4tb01897d.


DOI:10.1039/d4tb01897d
PMID:39835399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11747965/
Abstract

Branched peptide-based materials draw inspiration from dendritic structures to emulate the complex architecture of native tissues, aiming to enhance the performance of biomaterials in medical applications. These innovative materials benefit from several key features: they exhibit slower degradation rates, greater stiffness, and the ability to self-assemble. These properties are crucial for maintaining the structural integrity and functionality of the materials over time. By integrating bioactive peptides and natural polymers within their branched frameworks, these materials offer modularity and tunability and can accommodate a range of mechanical properties, degradation rates, and biological functions making them suitable for biomedical applications, including drug delivery systems, wound healing scaffolds, and tissue engineering constructs. In drug delivery, these materials can be engineered to release therapeutic agents in a controlled manner, enhancing the efficacy and safety of treatments. In wound healing, they provide a supportive environment which promotes rapid and efficient tissue repair. The combination of biomimetic design and functional adaptability makes branched peptide-based materials a promising candidate for the development of next-generation biomaterials, paving the way for significant advancements in healthcare.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/277c2d30f4e3/d4tb01897d-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/9171cc397088/d4tb01897d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/6f5c3ca5e78f/d4tb01897d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/334b7c114a3a/d4tb01897d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/c38a47f9a6d4/d4tb01897d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/05f693eb3f3c/d4tb01897d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/cd86a7877f4e/d4tb01897d-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/4257b10b8fc2/d4tb01897d-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/acb04c6afb6e/d4tb01897d-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/277c2d30f4e3/d4tb01897d-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/9171cc397088/d4tb01897d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/6f5c3ca5e78f/d4tb01897d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/334b7c114a3a/d4tb01897d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/c38a47f9a6d4/d4tb01897d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/05f693eb3f3c/d4tb01897d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/cd86a7877f4e/d4tb01897d-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/4257b10b8fc2/d4tb01897d-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/acb04c6afb6e/d4tb01897d-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e077/11747965/277c2d30f4e3/d4tb01897d-f9.jpg

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Evolution of branched peptides as novel biomaterials.

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本文引用的文献

[1]
Kinetic and Mechanistic Studies of Native Chemical Ligation with Phenyl α-Selenoester Peptides.

JACS Au. 2024-10-30

[2]
Tumor organoids for primary liver cancers: A systematic review of current applications in diagnostics, disease modeling, and drug screening.

JHEP Rep. 2024-7-1

[3]
Branched oncolytic peptides target HSPGs, inhibit metastasis, and trigger the release of molecular determinants of immunogenic cell death in pancreatic cancer.

Front Mol Biosci. 2024-10-2

[4]
Antibacterial and Anti-Inflammatory Activity of Branched Peptides Derived from Natural Host Defense Sequences.

J Med Chem. 2024-9-26

[5]
Kidney organoids: steps towards better organization and function.

Biochem Soc Trans. 2024-8-28

[6]
Safety-Catch Linkers for Solid-Phase Peptide Synthesis.

Molecules. 2024-3-22

[7]
Review: 3D cell models for organ-on-a-chip applications.

Anal Chim Acta. 2024-5-1

[8]
Peptide Dendrimer-Based Antibacterial Agents: Synthesis and Applications.

ACS Infect Dis. 2024-4-12

[9]
Glycan-Modified Peptides for Dual Inhibition of Human Immunodeficiency Virus Entry into Dendritic Cells and T Cells.

J Med Chem. 2024-3-14

[10]
Designing Multifunctional Biomaterials via Protein Self-Assembly.

Angew Chem Int Ed Engl. 2024-4-2

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