Evidence map›Paper›PMID 38363821›Full record

ArticleJournal of the American Chemical Society2024

Intracellular Delivery of Functional Proteins with DNA-Protein Nanogels-Lipids Complex.

Marina Mariconti, Laurie Dechamboux, Marion Heckmann, Julien Gros, Mathieu Morel, Virginie Escriou, Damien Baigl, Céline Hoffmann, Sergii Rudiuk

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. 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

9 authors.

Marina MaricontiPASTEUR, UMR8640, Department of Chemistry, PSL University, Sorbonne Université, CNRS, Ecole Normale Supérieure, Paris 75005 France.
Laurie DechambouxUniversité Paris Cité, CNRS, INSERM, UTCBS, Paris 75006, France.
Marion HeckmannUniversité Paris Cité, CNRS, INSERM, UTCBS, Paris 75006, France.
Julien GrosPASTEUR, UMR8640, Department of Chemistry, PSL University, Sorbonne Université, CNRS, Ecole Normale Supérieure, Paris 75005 France.
Mathieu MorelPASTEUR, UMR8640, Department of Chemistry, PSL University, Sorbonne Université, CNRS, Ecole Normale Supérieure, Paris 75005 France.ORCID 0000-0002-6284-1708
Virginie EscriouUniversité Paris Cité, CNRS, INSERM, UTCBS, Paris 75006, France.ORCID 0000-0001-5686-9301
Damien BaiglPASTEUR, UMR8640, Department of Chemistry, PSL University, Sorbonne Université, CNRS, Ecole Normale Supérieure, Paris 75005 France.ORCID 0000-0003-1772-3080
Céline HoffmannUniversité Paris Cité, CNRS, INSERM, UTCBS, Paris 75006, France.
Sergii RudiukPASTEUR, UMR8640, Department of Chemistry, PSL University, Sorbonne Université, CNRS, Ecole Normale Supérieure, Paris 75005 France.ORCID 0000-0003-1728-1163

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using functional proteins for therapeutic purposes due to their high selectivity and/or catalytic properties can enable the control of various cellular processes; however, the transport of active proteins inside living cells remains a major challenge. In contrast, intracellular delivery of nucleic acids has become a routine method for a number of applications in gene therapy, genome editing, or immunization. Here we report a functionalizable platform constituting of DNA-protein nanogel carriers cross-linked through streptavidin-biotin or streptactin-biotin interactions and demonstrate its applicability for intracellular delivery of active proteins. We show that the nanogels can be loaded with proteins bearing either biotin, streptavidin, or strep-tag, and the resulting functionalized nanogels can be delivered into living cells after complexation with cationic lipid vectors. We use this approach for delivery of alkaline phosphatase enzyme, which is shown to keep its catalytic activity after internalization by mouse melanoma B16 cells, as demonstrated by the DDAO-phosphate assay. The resulting functionalized nanogels have dimensions on the order of 100 nm, contain around 100 enzyme molecules, and are shown to be transfectable at low lipid concentrations (charge ratio

Indexed as

BiotinPolyethylene GlycolsAnimalsDNADrug CarriersLipidsMiceNanogelsProteinsStreptavidinBiotinDNADrug CarriersLipidsNanogelsPolyethylene GlycolsProteinsStreptavidin

Identifiers

PMID38363821
PMCPMC10910493

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.