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Journal ArticleDOI

Cell-penetrating peptides for the delivery of nucleic acids

Taavi Lehto, +2 more
- 20 Jun 2012 - 
- Vol. 9, Iss: 7, pp 823-836
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TLDR
This review will discuss recent advances of CPP-mediated delivery of nucleic acid-based cargo, concentrating on the delivery of plasmid DNA, splice-correcting ONs, and small-interfering RNAs.
Abstract
Introduction: Different gene therapy approaches have gained extensive interest lately and, after many initial hurdles, several promising approaches have reached to the clinics. Successful implementation of gene therapy is heavily relying on finding efficient measures to deliver genetic material to cells. Recently, non-viral delivery of nucleic acids and their analogs has gained significant interest. Among non-viral vectors, cell-penetrating peptides (CPPs) have been extensively used for the delivery of nucleic acids both in vitro and in vivo. Areas covered: In this review we will discuss recent advances of CPP-mediated delivery of nucleic acid-based cargo, concentrating on the delivery of plasmid DNA, splice-correcting ONs, and small-interfering RNAs. Expert opinion: CPPs have proved their potential as carriers for nucleic acids. However, similarly to other non-viral vectors, CPPs require further development, as efficient systemic delivery is still seldom achieved. To achieve this, CPPs should be modified...

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Journal ArticleDOI

Peptide-mediated delivery: an overview of pathways for efficient internalization

TL;DR: Recent advances in augmenting delivery efficacy and facilitation of endosomal escape of cargo are presented, and the cell-penetrating peptide-mediated delivery of two of the most popular classes of cargo molecules, oligonucleotides and proteins, is analyzed.
Journal ArticleDOI

Tissue-Specific Delivery of CRISPR Therapeutics: Strategies and Mechanisms of Non-Viral Vectors.

TL;DR: The most recent efforts towards novel non-viral delivery systems are discussed, focusing on strategies and mechanisms of peptide-based delivery systems, that can specifically deliver CRISPR components to different cell types for therapeutic and research purposes.
Journal ArticleDOI

Peptide-based vectors: recent developments.

TL;DR: This review focuses on peptide-based vectors for therapeutic molecules and on nucleic acid delivery, and reports in this review some of the latest strategies for peptides-mediated delivery of nucleic acids.
Journal ArticleDOI

MLCPP 2.0: An Updated Cell-penetrating Peptides and Their Uptake Efficiency Predictor.

TL;DR: Li et al. as mentioned in this paper proposed an interpretable stacking model that identifies CPPs and their strength of uptake efficiency, which achieved outstanding performance on the independent test set, significantly outperforming the existing state-of-the-art predictors.
References
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Journal ArticleDOI

Nanoparticle therapeutics: an emerging treatment modality for cancer

TL;DR: The features of nanoparticle therapeutics that distinguish them from previous anticancer therapies are highlighted, and how these features provide the potential for therapeutic effects that are not achievable with other modalities are described.
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Knocking down barriers: advances in siRNA delivery

TL;DR: An update on the progress of RNAi therapeutics is provided and novel synthetic materials for the encapsulation and intracellular delivery of nucleic acids are highlighted.
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A truncated HIV-1 Tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus

TL;DR: The main determinants required for Tat translocation within this sequence are delineated by synthesizing several peptides covering the Tat domain from residues 37 to 60 and the domain extending from amino acid 37 to 47, which corresponds to the α-helix structure, is not required for cellular uptake and for nuclear translocation.
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Design and development of polymers for gene delivery

TL;DR: With the growing understanding of polymer gene-delivery mechanisms and continued efforts of creative polymer chemists, it is likely that polymer-based gene-Delivery systems will become an important tool for human gene therapy.
Journal ArticleDOI

The third helix of the Antennapedia homeodomain translocates through biological membranes

TL;DR: It is reported here that a polypeptide of 16 amino acids in length corresponding to the third helix of the homeodomain deleted of its N-terminal glutamate is still capable of translocating through the membrane, suggesting an energy-independent mechanism of translocation not involving classical endocytosis.
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