Evidence map›Paper›PMID 41020188›Full record

ArticleEngineering in life sciences2025

Enhanced Cellular Uptake of Compact Cas Proteins: A Comparative Study of Cas12f and Cas9 in Human Cells.

Karim E Shalaby, Issam Hmila, S M Nasir Uddin, Nasser H Zawia, Omar M A El-Agnaf, Mustapha Aouida

Abstract read
In one paragraph

Article in Engineering in life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Karim E ShalabyLaboratory of Pluripotent Stem Cell Disease Modeling, Translational Medicine Department Research Branch, Sidra Medicine Doha Qatar.
Issam HmilaNeurological Disorder Research Center, Qatar Biomedical Research Institute (QBRI) Hamad Bin Khalifa University (HBKU), Qatar Foundation Doha Qatar.
S M Nasir UddinBiological and Biomedical Sciences Division College of Health & Life Sciences Hamad Bin Khalifa University Doha Qatar.
Nasser H ZawiaNeurological Disorder Research Center, Qatar Biomedical Research Institute (QBRI) Hamad Bin Khalifa University (HBKU), Qatar Foundation Doha Qatar.
Omar M A El-AgnafNeurological Disorder Research Center, Qatar Biomedical Research Institute (QBRI) Hamad Bin Khalifa University (HBKU), Qatar Foundation Doha Qatar.
Mustapha AouidaBiological and Biomedical Sciences Division College of Health & Life Sciences Hamad Bin Khalifa University Doha Qatar.ORCID https://orcid.org/0000-0001-7945-5320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical translation of CRISPR genome-editing therapies is often hindered by inefficient delivery of the CRISPR-Cas RNA-protein complex into target cells. The most widely used CRISPR-Cas9 system poses a significant challenge for efficient delivery into cells due to its large size (∼1.4 kDa). Recently reported compact Cas proteins, such as Cas12f (552 Da), Cas12k (639 Da), and Cas12m (596 Da) represent attractive alternatives as cargoes for delivery. In this brief research report, we employ efficient delivery vectors to evaluate the efficiency of cellular uptake of a compact Cas protein (Cas12f) compared to the widely used larger Cas9 in human cells. Our findings demonstrate that compact Cas proteins may facilitate more efficient cellular penetration and delivery, making them a promising alternative for the development of CRISPR-based therapies. Practical Application: Our study demonstrates that compact Cas proteins significantly enhance cellular uptake compared to larger Cas proteins. This improved uptake efficiency suggests that compact Cas proteins could be more effective for clinical application, where size constraints and delivery efficiency are critical challenges. Combined with the optimization and refinement of the editing efficiencies of compact Cas systems, our study provokes further exploration of compact Cas proteins in various therapeutic contexts to advance the development of more efficient CRISPR-based therapies.

Indexed as

Cas12fCas9CRISPRdeliveryribonucleoprotein (RNP)

Identifiers

PMID41020188
PMCPMC12464724

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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.