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1.
J Nanobiotechnology ; 22(1): 284, 2024 May 24.
Artigo em Inglês | MEDLINE | ID: mdl-38790037

RESUMO

CRISPR-based gene therapy offers precise targeting and specific editing of disease-related gene sequences, potentially yielding long-lasting treatment effects. However, efficient delivery remains a significant challenge for its widespread application. In this study, we design a novel short peptide-conjugated bioreducible polymer named TSPscp as a safe and effective delivery vector for the CRISPR system. Our results show that TSPscp markedly boosts transcriptional activation and genome editing activities of multiple CRISPR systems as confirmed by decomposition-seq and Deep-seq, which is resulted from its capability in facilitating delivery of plasmid DNA by promoting cellular uptake and lysosomal escape. Additionally, TSPscp further enhances genome editing of CRISPR by delivery of minicircle DNA, a condensed form of regular plasmid DNA. More importantly, TSPscp significantly improves delivery and genome editing of CRISPR system in vivo. In summary, our study highlights TSPscp as a promising delivery tool for CRISPR applications in vivo.


Assuntos
Sistemas CRISPR-Cas , Peptídeos Penetradores de Células , Edição de Genes , Plasmídeos , Edição de Genes/métodos , Humanos , Animais , Plasmídeos/genética , Peptídeos Penetradores de Células/química , Polímeros/química , Camundongos , Células HEK293 , Terapia Genética/métodos
2.
Nucleic Acids Res ; 50(D1): D928-D933, 2022 01 07.
Artigo em Inglês | MEDLINE | ID: mdl-34723320

RESUMO

As a means to aid in the investigation of viral infection mechanisms and identification of more effective antivirus targets, the availability of a source which continually collects and updates information on the virus and host ncRNA-associated interaction resources is essential. Here, we update the ViRBase database to version 3.0 (http://www.virbase.org/ or http://www.rna-society.org/virbase/). This update represents a major revision: (i) the total number of interaction entries is now greater than 820,000, an approximately 70-fold increment, involving 116 virus and 36 host organisms, (ii) it supplements and provides more details on RNA annotations (including RNA editing, RNA localization and RNA modification), ncRNA SNP and ncRNA-drug related information and (iii) it provides two additional tools for predicting binding sites (IntaRNA and PRIdictor), a visual plug-in to display interactions and a website which is optimized for more practical and user-friendly operation. Overall, ViRBase v3.0 provides a more comprehensive resource for virus and host ncRNA-associated interactions enabling researchers a more effective means for investigation of viral infections.


Assuntos
Bases de Dados Genéticas , Genoma Viral , Interações Hospedeiro-Patógeno/genética , RNA não Traduzido/genética , Software , Vírus/genética , Sítios de Ligação , Cromatina/química , Cromatina/metabolismo , Humanos , Internet , Anotação de Sequência Molecular , Polimorfismo de Nucleotídeo Único , Edição de RNA , RNA não Traduzido/classificação , RNA não Traduzido/metabolismo , Transdução de Sinais , Viroses/genética , Viroses/metabolismo , Viroses/patologia , Viroses/virologia , Vírus/classificação , Vírus/metabolismo , Vírus/patogenicidade
3.
Bioinformatics ; 2021 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-33471060

RESUMO

MOTIVATION: Ligand-receptor (L-R) interactions mediate cell adhesion, recognition and communication and play essential roles in physiological and pathological signaling. With the rapid development of single-cell RNA sequencing (scRNA-seq) technologies, systematically decoding the intercellular communication network involving L-R interactions has become a focus of research. Therefore, construction of a comprehensive, high-confidence and well-organized resource to retrieve L-R interactions in order to study the functional effects of cell-cell communications would be of great value. RESULTS: In this study, we developed Cellinker, a manually curated resource of literature-supported L-R interactions that play roles in cell-cell communication. We aimed to provide a useful platform for studies on cell-cell communication mediated by L-R interactions. The current version of Cellinker documents over 3,700 human and 3,200 mouse L-R protein-protein interactions (PPIs) and embeds a practical and convenient webserver with which researchers can decode intercellular communications based on scRNA-seq data. And over 400 endogenous small molecule (sMOL) related L-R interactions were collected as well. Moreover, to help with research on coronavirus (CoV) infection, Cellinker collects information on 16 L-R PPIs involved in CoV-human interactions (including 12 L-R PPIs involved in SARS-CoV-2 infection). In summary, Cellinker provides a user-friendly interface for querying, browsing and visualizing L-R interactions as well as a practical and convenient web tool for inferring intercellular communications based on scRNA-seq data. We believe this platform could promote intercellular communication research and accelerate the development of related algorithms for scRNA-seq studies. AVAILABILITY: Cellinker is available at http://www.rna-society.org/cellinker/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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