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Intracellular Protein Delivery: Approaches, Challenges, and Clinical Applications.

作者信息

Chan Alexander, Tsourkas Andrew

机构信息

Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

BME Front. 2024 Jan 25;5:0035. doi: 10.34133/bmef.0035. eCollection 2024.


DOI:10.34133/bmef.0035
PMID:38282957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10809898/
Abstract

Protein biologics are powerful therapeutic agents with diverse inhibitory and enzymatic functions. However, their clinical use has been limited to extracellular applications due to their inability to cross plasma membranes. Overcoming this physiological barrier would unlock the potential of protein drugs for the treatment of many intractable diseases. In this review, we highlight progress made toward achieving cytosolic delivery of recombinant proteins. We start by first considering intracellular protein delivery as a drug modality compared to existing Food and Drug Administration-approved drug modalities. Then, we summarize strategies that have been reported to achieve protein internalization. These techniques can be broadly classified into 3 categories: physical methods, direct protein engineering, and nanocarrier-mediated delivery. Finally, we highlight existing challenges for cytosolic protein delivery and offer an outlook for future advances.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/fe043863b2d5/bmef.0035.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/8ea52426a82a/bmef.0035.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/0897149bb861/bmef.0035.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/ed50071bc3fd/bmef.0035.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/b3635efb27a0/bmef.0035.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/25e97b1e361b/bmef.0035.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/e8b2b0f0fcb2/bmef.0035.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/fe043863b2d5/bmef.0035.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/8ea52426a82a/bmef.0035.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/0897149bb861/bmef.0035.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/ed50071bc3fd/bmef.0035.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/b3635efb27a0/bmef.0035.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/25e97b1e361b/bmef.0035.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/e8b2b0f0fcb2/bmef.0035.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1d/10809898/fe043863b2d5/bmef.0035.fig.007.jpg

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Intracellular Protein Delivery: Approaches, Challenges, and Clinical Applications.

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本文引用的文献

[1]
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[2]
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Biomedicines. 2023-7-24

[3]
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[4]
Genome editing in the mouse brain with minimally immunogenic Cas9 RNPs.

Mol Ther. 2023-8-2

[5]
DARPins bind their cytosolic targets after having been translocated through the protective antigen pore of anthrax toxin.

Sci Rep. 2023-5-17

[6]
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Nat Biomed Eng. 2023-5

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Immunooncol Technol. 2023-3-9

[8]
Kinase-Modulated Bioluminescent Indicators Enable Noninvasive Imaging of Drug Activity in the Brain.

ACS Cent Sci. 2023-3-20

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Lipid Nanoparticle Delivery of Small Proteins for Potent RAS Inhibition.

ACS Appl Mater Interfaces. 2023-5-10

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Nat Biotechnol. 2024-2

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