Evidence map›Paper›PMID 40342143›Full record

ArticleBiotechnology and bioengineering2025

Cell-Penetrating Peptide-Based Triple Nanocomplex Enables Efficient Nuclear Gene Delivery in Chlamydomonas reinhardtii.

Eun Jeong Sim, Quynh-Giao Tran, Yu Rim Lee, Trang Thi Le, Hyang Ran Yoon, Dong-Yun Choi, Dae-Hyun Cho, Jin-Ho Yun, Hong Il Choi, Hee-Sik Kim and 1 more

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

11 authors.

Eun Jeong SimCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Quynh-Giao TranCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Yu Rim LeeCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Trang Thi LeCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Hyang Ran YoonImmunotherapy Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Dong-Yun ChoiCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Dae-Hyun ChoCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Jin-Ho YunCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Hong Il ChoiCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Hee-Sik KimCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
Yong Jae LeeCell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0001-9917-8199

Funding

This study was supported by Basic Science Research Program, National Research Foundation of Korea (Grants RS-2024-00351663 (HSK), 2021R1C1C1003425 (YJL), RS-2024-00353284 (HIC)), and also supported by the KRIBB Research Initiative Program, Korea Research Institute of Bioscience and Biotechnology (Grant KGM5252423 (HSK)).
6 · The paper itself

Abstract

Microalgae are a promising solution for mitigating climate change due to their ability to capture greenhouse gases and produce renewable materials. However, their effective application is often hindered by barriers that necessitate advances in genetic engineering to improve photosynthesis and productivity. One major obstacle is the microalgal cell wall, which complicates the delivery of genetic material into these organisms. To address these challenges, we developed a novel triple nanocomplex system integrating cell-penetrating peptides (CPPs), nuclear localization signal (NLS) peptides, and plasmid DNA. This system allows simple preparation while achieving efficient nuclear translocation of plasmid DNA. We evaluated two CPPs, pVEC-ORI and pVEC-R6A, for their efficacy in facilitating intracellular transfer of DNA into wild-type Chlamydomonas reinhardtii cells. Notably, pVEC-R6A demonstrated a 6.88-fold increase in efficiency compared to pVEC-ORI, despite the presence of thick cell walls. The optimal CPP:DNA ratio for stable nanocomplex formation was determined to be 5:1 for pVEC-ORI and 10:1 for pVEC-R6A. By incorporating the simian virus 40 (SV40) NLS into CPP/DNA nanocomplexes, we successfully directed the localization of plasmid DNA into the nucleus. Our findings indicate that this simple and efficient DNA delivery system has significant potential as a tool to advance microalgal synthetic biology.

Indexed as

Cell NucleusCell-Penetrating PeptidesChlamydomonas reinhardtiiGene Transfer TechniquesNuclear Localization SignalsPlasmidsCell-Penetrating PeptidesNuclear Localization Signalscell‐penetrating peptidegene deliverymicroalgaenanocomplexnuclear localization signalpVECSV40

Identifiers

PMID40342143
PMCPMC12235220

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.