Executive Summary
have emerged as versatile platforms for delivering therapeutic agents by X Jiang·2025·Cited by 4—Tiger nut protein fibrils (TNPFs) were prepared through three pathways: self-assembly (TNPF), Homogeneous nuclei (HN)-induced (HN-TNPF),
Peptide nanofibrils (PNFs), particularly those explored under the umbrella of HPNF, represent a fascinating class of self-assembling biomaterials with a growing impact across various scientific disciplines. These structures, formed from peptides and amino acids, exhibit remarkable versatility, stemming from their ability to self-assemble into ordered fibrillar architectures. Their prevalence in nature, where they play crucial roles in both physiological and pathological processes, highlights their inherent biocompatibility and functional potential. This article delves into the intricate world of peptide nanofibrils, exploring their formation, properties, and cutting-edge applications, with a particular focus on their role as enhancers in gene transfer technologies.
The self-assembly of supramolecular nanofibrils is a fundamental process driving the formation of PNFs. This spontaneous organization occurs through non-covalent interactions, primarily hydrogen bonding between the amide groups (C=O and NH) of neighboring peptides, leading to the formation of a stable, extended H-bonded network. This intricate process allows for the creation of highly ordered structures with tunable characteristics. The resulting nanofibrils possess a unique morphology that dictates their functional properties. For instance, the structural morphology of peptide nanofibrils has been shown to influence viral transduction efficiencies.
One of the most significant applications emerging for peptide nanofibrils is their use as transduction enhancers, particularly in gene therapy. Research has demonstrated that peptide nanofibrils (PNFs) can significantly boost retroviral gene transfer. These self-assembling nanostructures act by binding to negatively charged virions, thereby facilitating their interaction with target cells and enhancing the efficiency of gene delivery. This mechanism is crucial for improving the efficacy of gene therapy vectors, making them more potent and reliable. Studies have highlighted that PNFs can increase retroviral gene transfer even more efficiently than other enhancers like SEVI, while also being easy to produce and handle, and appearing safe in preclinical assessments.
The development of optimized peptide nanofibrils is a key area of research. For example, D4 PNFs have been identified as an economical and straightforward nanotechnological tool for refining ex vivo gene transfer, particularly in the production of CAR-T cells. The ability to tailor the peptide sequence and structure allows for the creation of PNFs with specific functionalities, such as enhancing viral vector delivery in ex vivo gene therapy applications. Furthermore, peptide nanofibrils have emerged as versatile platforms for delivering therapeutic agents due to their inherent biocompatibility and tunable characteristics. This opens doors for their application in drug delivery systems, where they can encapsulate and deliver therapeutic molecules to specific sites within the body.
Beyond gene therapy, the applications of peptide nanofibrils extend to other areas. For instance, certain peptides are known to possess antimicrobial properties by forming nanofibrils that can entrap pathogens and disrupt cellular membranes. This has led to investigations into their potential as antimicrobial agents. Additionally, hPNFs created via a facile self-assembly route are being explored for various biomedical applications, showcasing the broad potential of these engineered biomaterials. The ease of their production and their inherent biocompatibility make them attractive candidates for a wide range of innovative technologies.
In summary, peptide nanofibrils (HPNF) represent a rapidly evolving field with immense potential. Their ability to self-assemble into highly ordered structures, coupled with their biocompatibility and tunable properties, positions them as critical components in advanced biotechnological applications, from enhancing gene therapy to developing novel antimicrobial agents. The ongoing research into their formation, characterization, and functionalization promises to unlock even more groundbreaking uses for these remarkable nanofibrils.
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