Evidence map›Paper›PMID 38630829›Full record

ArticleScience advances2024

Dual-responsive nanocarriers for efficient cytosolic protein delivery and CRISPR-Cas9 gene therapy of inflammatory skin disorders.

Echuan Tan, Tao Wan, Qi Pan, Jianan Duan, Song Zhang, Ruijue Wang, Peng Gao, Jia Lv, Hui Wang, Dali Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
20.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 45 citations in OpenAlex.

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  20. Toward Artificial Peptide Nanocapsules.Nano-micro letters · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Echuan TanShanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, China.ORCID 0000-0001-5545-2272
Tao WanLiangzhu Laboratory, Zhejiang University Medical Center, Hangzhou 311121, China.ORCID 0000-0002-8299-8921
Qi PanCollege of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0000-0002-1852-1387
Jianan DuanSouth China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China.
Song ZhangSouth China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China.ORCID 0000-0003-4842-9159
Ruijue WangSouth China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China.
Peng GaoSouth China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China.ORCID 0000-0002-3839-3167
Jia LvShanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, China.
Hui WangSouth China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China.
Dali LiShanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, China.ORCID 0000-0002-0046-8493
Yuan PingLiangzhu Laboratory, Zhejiang University Medical Center, Hangzhou 311121, China.ORCID 0000-0003-2571-7721
Yiyun ChengShanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, China.ORCID 0000-0001-6019-5645
South China University of Technology · CNEast China Normal University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing protein drugs that can target intracellular sites remains a challenge due to their inadequate membrane permeability. Efficient carriers for cytosolic protein delivery are required for protein-based drugs, cancer vaccines, and CRISPR-Cas9 gene therapies. Here, we report a screening process to identify highly efficient materials for cytosolic protein delivery from a library of dual-functionalized polymers bearing both boronate and lipoic acid moieties. Both ligands were found to be crucial for protein binding, endosomal escape, and intracellular protein release. Polymers with higher grafting ratios exhibit remarkable efficacies in cytosolic protein delivery including enzymes, monoclonal antibodies, and Cas9 ribonucleoprotein while preserving their activity. Optimal polymer successfully delivered Cas9 ribonucleoprotein targeting

Indexed as

CRISPR-Cas SystemsGene EditingAnimalsGenetic TherapyGene Transfer TechniquesMiceNLR Family, Pyrin Domain-Containing 3 ProteinPolymersRibonucleoproteinsNLR Family, Pyrin Domain-Containing 3 ProteinPolymersRibonucleoproteins

Identifiers

PMID38630829
PMCPMC11023524
OpenAlexW4394872662

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.