Single-molecule live-cell RNA imaging with CRISPR–Csm DOI Creative Commons
Chenglong Xia, David Colognori, X. Jiang

и другие.

Nature Biotechnology, Год журнала: 2025, Номер unknown

Опубликована: Фев. 18, 2025

Abstract Understanding the diverse dynamic behaviors of individual RNA molecules in single cells requires visualizing them at high resolution real time. However, single-molecule live-cell imaging unmodified endogenous has not yet been achieved a generalizable manner. Here, we present fluorescence situ hybridization (smLiveFISH), robust approach that combines programmable RNA-guided, RNA-targeting CRISPR–Csm complex with multiplexed guide RNAs for direct and efficient visualization range cell types, including primary cells. Using smLiveFISH, track native NOTCH2 MAP1B transcripts living identify two distinct localization mechanisms cotranslational translocation mRNA endoplasmic reticulum directional transport toward periphery. This method potential to unlock principles governing spatiotemporal organization health disease.

Язык: Английский

Light‐Guided Genetic Scissors Based on Phosphorene Quantum Dot DOI
Zhi Chen, Hao Huang,

Jiefeng Deng

и другие.

Laser & Photonics Review, Год журнала: 2024, Номер 18(11)

Опубликована: Июль 10, 2024

Abstract Genetic engineering faces persistent challenges in achieving precise Deoxyribonucleic acid (DNA) cleavage, especially with the limitations associated current enzyme‐based methods, exemplified by issues CRISPR technologies. This study introduces a groundbreaking approach: utilizing reactive oxygen species (ROS) generated Multiphoton Absorption (MPA)‐excited Black Phosphorus Quantum Dots (BPQDs) under femto‐second laser irradiation. innovative method not only allows excitation lower energy but also enhances overall efficiency. The integration of complementary RNA sequences facilitates high‐efficiency, site‐selective DNA cleavage system, named “TADPOLE” (Targeted Precision Oriented Laser Excision). Beyond its precision targeting arbitrary using quantum dots, TADPOLE harnesses unique multiphoton absorption property BPQDs, enabling lower‐energy light sources suitable for vivo applications future. Moreover, approach integrates guiding and ultrafast technology to provide control over local ROS generation minimal heat production. guarantees site‐specific while mitigating risk damage non‐targeted sequences. In summary, this catalyzes advancements enzyme‐free technologies, transformative implications genetic engineering, biotechnology, medicine. holistic precision, versatility, endurance presented open new avenues targeted gene therapies related fields.

Язык: Английский

Процитировано

34

Rapid DNA unwinding accelerates genome editing by engineered CRISPR-Cas9 DOI Creative Commons
Amy R. Eggers, Kai Chen, Katarzyna M. Soczek

и другие.

Cell, Год журнала: 2024, Номер 187(13), С. 3249 - 3261.e14

Опубликована: Май 22, 2024

Thermostable clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas9) enzymes could improve genome-editing efficiency delivery due to extended protein lifetimes. However, initial experimentation demonstrated Geobacillus stearothermophilus Cas9 (GeoCas9) be virtually inactive when used in cultured human cells. Laboratory-evolved variants of GeoCas9 overcome this natural limitation by acquiring mutations the wedge (WED) domain that produce >100-fold-higher levels. Cryoelectron microscopy (cryo-EM) structures wild-type improved (iGeoCas9) reveal contacts between WED iGeoCas9 DNA substrates. Biochemical analysis shows accelerates unwinding capture substrates under magnesium-restricted conditions typical mammalian but not bacterial These findings enabled rational engineering other orthologs enhance levels, pointing a general strategy for editing enzyme improvement. Together, these results uncover new role demonstrate how accelerated target dramatically improves Cas9-induced activity.

Язык: Английский

Процитировано

30

Size exclusion chromatography of biopharmaceutical products: From current practices for proteins to emerging trends for viral vectors, nucleic acids and lipid nanoparticles DOI Creative Commons

Valentina D’Atri,

Mateusz Imiołek,

Colette F. Quinn

и другие.

Journal of Chromatography A, Год журнала: 2024, Номер 1722, С. 464862 - 464862

Опубликована: Апрель 1, 2024

The 21st century has been particularly productive for the biopharmaceutical industry, with introduction of several classes innovative therapeutics, such as monoclonal antibodies and related compounds, gene therapy products, RNA-based modalities. All these new molecules are susceptible to aggregation fragmentation, which necessitates a size variant analysis their comprehensive characterization. Size exclusion chromatography (SEC) is one reference techniques that can be applied. analytical mAbs now well established some them emerging newer In this context, objective review article is: i) provide short historical background on SEC, ii) suggest clear guidelines selection packing material mobile phase successful method development in modern SEC; iii) highlight recent advances use narrow-bore micro-bore columns, ultra-wide pore low-adsorption column hardware. Some important innovations, recycling coupling SEC mass spectrometry, alternative detectors charge detection spectrometry photometry also described. addition, discusses multidimensional setups shows most at preparative scale. third part article, possibility characterization modalities reviewed. final summary opportunities limitations different products.

Язык: Английский

Процитировано

29

Unraveling host regulation of gut microbiota through the epigenome–microbiome axis DOI Creative Commons
Michael Le Pepke, Søren B. Hansen, Morten T. Limborg

и другие.

Trends in Microbiology, Год журнала: 2024, Номер 32(12), С. 1229 - 1240

Опубликована: Июнь 5, 2024

Recent studies of dynamic interactions between epigenetic modifications a host organism and the composition or activity its associated gut microbiota suggest an opportunity for to shape microbiome through alterations that lead changes in gene expression noncoding RNA activity. We use insights from microbiota-induced review potential epigenetically regulate microbiome, which bidirectional 'epigenome–microbiome axis' emerges. This axis embeds environmentally induced variation, may influence adaptive evolution host–microbe interactions. furthermore present our perspective on how epigenome–microbiome can be understood investigated within holo-omic framework with applications applied health food sciences.

Язык: Английский

Процитировано

24

A roadmap for affordable genetic medicines DOI
Melinda Kliegman, Manar Zaghlula,

Susan L. Abrahamson

и другие.

Nature, Год журнала: 2024, Номер 634(8033), С. 307 - 314

Опубликована: Июль 17, 2024

Язык: Английский

Процитировано

23

CRISPR/Cas12a-based biosensors for environmental monitoring and diagnostics DOI Creative Commons
Atif Khurshid Wani, Nahid Akhtar, Tahir ul Gani Mir

и другие.

Environmental Technology & Innovation, Год журнала: 2024, Номер 34, С. 103625 - 103625

Опубликована: Апрель 4, 2024

Contaminants, such as nucleic acids or toxic small molecules, threaten both human health and ecosystems when they infiltrate the environment. The precise highly sensitive identification of contaminants holds paramount importance across diverse domains, including safeguarding food integrity, facilitating clinical diagnostics, monitoring environmental conditions. Traditional methodologies, encompassing spectroscopy, chromatography, sequencing, metagenomics, have conventionally served pivotal roles in detection processes. Nevertheless, these methods encountered recurring challenges related to sensitivity, specificity, portability. This review focuses on groundbreaking CRISPR/Cas12-based biosensors. These biosensors leverage incredible precision programmability CRISPR/Cas system recognize specific targets. Here, we comprehensively assess fundamental mechanisms that enable detection, ranging from guide RNA design collateral cleavage. versatility CRISPR/Cas12 becomes evident through their applications. applications encompass medical safety, monitoring. transition conventional ultimately represents a significant milestone contaminant detection. By incorporating molecular biology, nanotechnology, bioinformatics, potential reshape landscape water CRIPSR-Cas diagnostics is transformative technology paves way for safer healthier future environment life.

Язык: Английский

Процитировано

22

The pAblo·pCasso self-curing vector toolset for unconstrained cytidine and adenine base-editing in Gram-negative bacteria DOI Creative Commons
Ekaterina Kozaeva,

Zacharias S. Nielsen,

Manuel Nieto‐Domínguez

и другие.

Nucleic Acids Research, Год журнала: 2024, Номер 52(4), С. e19 - e19

Опубликована: Янв. 5, 2024

Abstract A synthetic biology toolkit, exploiting clustered regularly interspaced short palindromic repeats (CRISPR) and modified CRISPR-associated protein (Cas) base-editors, was developed for genome engineering in Gram-negative bacteria. Both a cytidine base-editor (CBE) an adenine (ABE) have been optimized precise single-nucleotide modification of plasmid targets. CBE comprises deaminase conjugated to Cas9 nickase from Streptococcus pyogenes (SpnCas9), resulting C→T (or G→A) substitutions. Conversely, ABE consists fused SpnCas9 A→G T→C) editing. Several nucleotide substitutions were achieved using these plasmid-borne base-editing systems novel protospacer adjacent motif (PAM)-relaxed (SpRY) variant. Base-editing validated Pseudomonas putida other bacteria by inserting premature STOP codons into target genes, thereby inactivating both fluorescent proteins metabolic (antibiotic-resistance) functions. The functional knockouts obtained via reverted the wild-type genotype ABE. Additionally, series induction-responsive vectors facilitate curing platform single cultivation step, simplifying complex strain programs without relying on homologous recombination yielding plasmid-free, bacterial cells.

Язык: Английский

Процитировано

21

Engineering self-deliverable ribonucleoproteins for genome editing in the brain DOI Creative Commons
Kai Chen, Elizabeth C. Stahl, Min Hyung Kang

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Фев. 26, 2024

The delivery of CRISPR ribonucleoproteins (RNPs) for genome editing in vitro and vivo has important advantages over other methods, including reduced off-target immunogenic effects. However, effective RNPs remains challenging certain cell types due to low efficiency toxicity. To address these issues, we engineer self-deliverable that can promote efficient cellular uptake carry out robust without the need helper materials or biomolecules. Screening cell-penetrating peptides (CPPs) fused CRISPR-Cas9 protein identifies potent constructs capable neural progenitor cells. Further engineering fusion proteins establishes a C-terminal Cas9 with three copies A22p, peptide derived from human semaphorin-3a, exhibits substantially improved efficacy compared constructs. We find generate edits clinically relevant genes when injected directly into mouse striatum. Overall, provide facile platform vivo.

Язык: Английский

Процитировано

21

Precise fine-turning of GhTFL1 by base editing tools defines ideal cotton plant architecture DOI Creative Commons
Guanying Wang, Fuqiu Wang, Zhongping Xu

и другие.

Genome biology, Год журнала: 2024, Номер 25(1)

Опубликована: Фев. 26, 2024

CRISPR/Cas-derived base editor enables precise editing of target sites and has been widely used for basic research crop genetic improvement. However, the efficiency editors at different targets varies greatly.

Язык: Английский

Процитировано

21

Revisiting growth–defence trade‐offs and breeding strategies in crops DOI Creative Commons
Mingjun Gao,

Zeyun Hao,

Yuese Ning

и другие.

Plant Biotechnology Journal, Год журнала: 2024, Номер 22(5), С. 1198 - 1205

Опубликована: Фев. 27, 2024

Plants have evolved a multi-layered immune system to fight off pathogens. However, activation is costly and often associated with growth development penalty. In crops, yield the main breeding target usually affected by high disease resistance. Therefore, proper balance between defence critical for achieving efficient crop improvement. This review highlights recent advances in attempts designed alleviate trade-offs resistance crops mediated (R) genes, susceptibility (S) genes pleiotropic genes. We also provide an update on strategies optimizing growth-defence breed future desirable yield.

Язык: Английский

Процитировано

21