Evidence map›Paper›PMID 36986744›Full record

ArticlePharmaceutics2023

Modification of the Linker Amino Acid in the Cell-Penetrating Peptide NickFect55 Leads to Enhanced pDNA Transfection for In Vivo Applications.

Heleri H Härk, Ly Porosk, Lucas R de Mello, Piret Arukuusk, Emerson R da Silva, Kaido Kurrikoff

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Heleri H HärkInstitute of Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.ORCID 0000-0001-6004-1814
Ly PoroskInstitute of Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.ORCID 0000-0002-4664-4560
Lucas R de MelloDepartamento de Biofisica, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.
Piret ArukuuskInstitute of Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.
Emerson R da SilvaDepartamento de Biofisica, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.ORCID 0000-0001-5876-2276
Kaido KurrikoffInstitute of Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.ORCID 0000-0002-5161-8930

Funding

University of Tartu Feasibility Fund 2014-2020.4.01.15-0013
6 · The paper itself

Abstract

Despite numerous efforts over the last three decades, nucleic acid-based therapeutics still lack delivery platforms in the clinical stage. Cell-penetrating peptides (CPPs) may offer solutions as potential delivery vectors. We have previously shown that designing a "kinked" structure in the peptide backbone resulted in a CPP with efficient in vitro transfection properties. Further optimization of the charge distribution in the C-terminal part of the peptide led to potent in vivo activity with the resultant CPP NickFect55 (NF55). Currently, the impact of the linker amino acid was further investigated in the CPP NF55, with the aim to discover potential transfection reagents for in vivo application. Taking into account the expression of the delivered reporter in the lung tissue of mice, and the cell transfection in the human lung adenocarcinoma cell line, the new peptides NF55-Dap and NF55-Dab* have a high potential for delivering nucleic acid-based therapeutics to treat lung associated diseases, such as adenocarcinoma.

Indexed as

cell-penetrating peptidesin vivo transfectionpDNA delivery

Identifiers

PMID36986744
PMCPMC10051810

What OpenQuestion holds

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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.