» Articles » PMID: 37572220

Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy

Overview
Journal Nanomicro Lett
Publisher Springer
Date 2023 Aug 12
PMID 37572220
Authors
Affiliations
Soon will be listed here.
Abstract

Gene therapy offers potentially transformative strategies for major human diseases. However, one of the key challenges in gene therapy is developing an effective strategy that could deliver genes into the specific tissue. Here, we report a novel virus-like nanoparticle, the bioorthgonal engineered virus-like recombinant biosome (reBiosome), for efficient gene therapies of cancer and inflammatory diseases. The mutant virus-like biosome (mBiosome) is first prepared by site-specific codon mutation for displaying 4-azido-L-phenylalanine on vesicular stomatitis virus glycoprotein of eBiosome at a rational site, and the reBiosome is then prepared by clicking weak acid-responsive hydrophilic polymer onto the mBiosome via bioorthogonal chemistry. The results show that the reBiosome exhibits reduced virus-like immunogenicity, prolonged blood circulation time and enhanced gene delivery efficiency to weakly acidic foci (like tumor and arthritic tissue). Furthermore, reBiosome demonstrates robust therapeutic efficacy in breast cancer and arthritis by delivering gene editing and silencing systems, respectively. In conclusion, this study develops a universal, safe and efficient platform for gene therapies for cancer and inflammatory diseases.

Citing Articles

Research advancements in nanoparticles and cell-based drug delivery systems for the targeted killing of cancer cells.

Abdessalem M, Adham S Oncol Res. 2024; 33(1):27-44.

PMID: 39735681 PMC: 11671623. DOI: 10.32604/or.2024.056955.


CAR T Cell Nanosymbionts: Revealing the Boundless Potential of a New Dyad.

Baena J, Perez L, Toro-Pedroza A, Kitawaki T, Loukanov A Int J Mol Sci. 2024; 25(23).

PMID: 39684867 PMC: 11642191. DOI: 10.3390/ijms252313157.


Current advance of nanotechnology in diagnosis and treatment for malignant tumors.

Wang B, Hu S, Teng Y, Chen J, Wang H, Xu Y Signal Transduct Target Ther. 2024; 9(1):200.

PMID: 39128942 PMC: 11323968. DOI: 10.1038/s41392-024-01889-y.


Self-Penetrating Oligonucleotide Derivatives: Features of Self-Assembly and Interactions with Serum and Intracellular Proteins.

Bauer I, Ilina E, Zharkov T, Grigorieva E, Chinak O, Kupryushkin M Pharmaceutics. 2023; 15(12).

PMID: 38140119 PMC: 10747088. DOI: 10.3390/pharmaceutics15122779.


Anti-Acidification and Immune Regulation by Nano-Ceria-Loaded Mg-Al Layered Double Hydroxide for Rheumatoid Arthritis Therapy.

Fu H, Guo Y, Fang W, Wang J, Hu P, Shi J Adv Sci (Weinh). 2023; 11(6):e2307094.

PMID: 38064119 PMC: 10853726. DOI: 10.1002/advs.202307094.

References
1.
Schnell J, Chou J . Structure and mechanism of the M2 proton channel of influenza A virus. Nature. 2008; 451(7178):591-5. PMC: 3108054. DOI: 10.1038/nature06531. View

2.
Mejia-Mendez J, Vazquez-Duhalt R, Hernandez L, Sanchez-Arreola E, Bach H . Virus-like Particles: Fundamentals and Biomedical Applications. Int J Mol Sci. 2022; 23(15). PMC: 9369363. DOI: 10.3390/ijms23158579. View

3.
Moser B, Clark-Lewis I, Zwahlen R, Baggiolini M . Neutrophil-activating properties of the melanoma growth-stimulatory activity. J Exp Med. 1990; 171(5):1797-802. PMC: 2187876. DOI: 10.1084/jem.171.5.1797. View

4.
CARR M, Roth S, Luther E, ROSE S, Springer T . Monocyte chemoattractant protein 1 acts as a T-lymphocyte chemoattractant. Proc Natl Acad Sci U S A. 1994; 91(9):3652-6. PMC: 43639. DOI: 10.1073/pnas.91.9.3652. View

5.
Stuart D, Gouet P . Viral envelope glycoproteins swing into action. Structure. 1995; 3(7):645-8. DOI: 10.1016/s0969-2126(01)00199-x. View