Redox Biology
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2025
·
IF 11.9
Xue Shi,Yun Zhao,Hong-Yu Gao,Wei Yang,Jun Liao,Hui-Han Wang,Xiao-Tian Wang,Wei Yan
Diffuse large B cell lymphoma (DLBCL) is a common hematologic malignancy. NFS1 cysteine desulfurase, as a rate-limiting enzyme in the iron-sulfur cluster (ISC) biogenesis, has been reported to be associated with tumor progression. However, the role of NFS1 in DLBCL remains elusive. Here, we showed an upregulation of NFS1 in DLBCL tumor tissues. Knockdown of NFS1 decreased the cell viability and enhanced LDH levels in DLBCL cells. Animal experiments further indicated that downregulation of NFS1 suppresses tumor growth in vivo. NFS1 knockdown increased the lipid reactive oxygen species (ROS) level in cells, and this promotional effect was reversed by ferroptosis inhibitors, but not influenced by other types of cell death inhibitors. This result suggested that NFS1 depletion-impaired cell viability is associated with ferroptosis. Silenced NFS1 aggravated ferroptosis inducers caused cell viability inhibition, lactate dehydrogenase (LDH), and lipid ROS levels enhancement, while the addition of ferroptosis inhibitors abated these trends. Moreover, catalytic residue mutation of NFS1 did not affect its protein expression but decreased the cell viability, which was promoted by NFS1 upregulation, indicating that the protective effect of NFS1 in DLBCL cells was related to its catalytic activity. Further results showed that frataxin (FXN), the upstream activator of NFS1, reduced the cell viability in NFS1 upregulated cells. Consistent with NFS1, FXN silencing aggravated erastin-induced cell viability inhibition and LDH level enhancement. Silencing NFS1 or FXN inhibited the level of iron ions storage-related proteins but promoted the level of transport-related proteins. In addition, silenced NFS1 or FXN displayed an inhibition effect on protein expression of DNA polymerases, but a promotion trend in the phosphorylation of DNA damage markers. In conclusion, we demonstrated that ISC-related proteins NFS1 and FXN protect DLBCL cells from ferroptosis and DNA damage, thus exhibiting an essential role in DLBCL progression.
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高影响因子
JOURNAL OF FLUORESCENCE
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2025
·
IF 3.1
Fang Fang,Cao Hongyu,Lu Jialu,Chen Nannan,Zhang Lu,Chen Yang
Carbon dots (CDs)-based ratiometric fluorescence strategies have attracted considerable attention. In this study, we developed a facile ratiometric fluorescent biosensor for DNA detection by utilizing the blue-emitting carbon dots (BCDs) as the fluorophore and acriflavine (AF), a fluorescent biological stain reagent, as both the response and recognition molecules. When AF was added, the fluorescence of BCDs decreased effectively and accompanied by a hypsochromic shift from 448 to 425 nm, whereas the fluorescence of AF at about 500 nm appeared due to the synergistic effect of Förster resonance energy transfer (FRET) and the inner filter effect (IFE) between the BCDs and AF. In the presence of DNA, the intercalative binding of AF into the DNA helix resulted in the fluorescence quenching of AF and the fluorescence restoration of BCDs at the same time. Therefore, the quantitative detection of DNA can be carried out vis evaluating the fluorescence intensity ratio of F 425 /F 500 . Under optimized conditions, the developed fluorescence method had an excellent linear range from 0 to 90 µM and a low detection limit of 0.52 µM. In addition, satisfactory results were obtained for the analysis of DNA in synthetic and real samples, with spiked recoveries ranging from 90.1 to 101.3%, demonstrating the enormous potential of the developed sensing platform for bioanalysis and biodetection. Graphical
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JOURNAL OF MOLECULAR STRUCTURE
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2025
·
IF 4.7
Yunkai Sun,Qingqing Song,Meng Cao,Chunhong Tan,Xiao-Feng Wang,Kejie Du,Yuheng Zhang,Yi Ding,Xiaoqiang Xue
Metal-organic complexes, particularly copper complexes, are emerging as promising candidates for anticancer drug due to their versatile redox states. Two copper complexes ( complex1 and complex2 ) have been designed based on the ligands for 1,10-phenanthroline (phen), 4,5-diazofluoren-9-one (DAFO) and 1,4-terephthalic acid (1,4-BDC), and the structures have been determined by X-ray single crystal analysis. The interactions of the complexes with calf thymus DNA (CT-DNA) have been investigated using UV-vis absorption and viscosity measurements. The results indicate that the complex 1 and complex 2 respectively bind to CT-DNA, and the binding mode of the former is in electrostatic binding or groove mode, while that of the latter is in insertion mode. The complex 2 had better activity to break CT-DNA than complex 1 .
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ANALYTICAL CHEMISTRY
·
2024
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IF 6.7
Xinyue Jia,Jiayang He,Mengdie Li,Jingjing Ye,Yuqing Zhang,Chunli Yang,Ruo Yuan,Wenju Xu
Exploring the ability of four-stranded DNA nanorings (fsDNRs) to host multiple nanosilver clusters (NAgCs) for cooperatively amplifiable fluorescence biosensing to a specific initiator (tI*) is fascinating. By designing three DNA single strands and three analogous stem-loop hairpins, we developed a functional fsDNR through sequential cross-opening and overlapped hybridization. Note that a substrate strand (SS) was programmed with six modules: two severed splits (sT and sT′) of NAgCs template, two sequestered segments by a middle unpaired spacer, and a partition for tI*-recognizable displacement, while sT and sT′ were also tethered in two ends of three hairpins. At first, a triple dsDNA complex with stimulus-responsiveness was formed to guide the specific binding to tI*, while the exposed toehold of the SS activated the forward cascade hybridization of three hairpins, until the ring closure in the tailored self-assembly pathway for forming the fsDNR. The resulting four duplexes forced each pair of sT/sT′ to be merged as the parent template in four nicks, guiding the preferential synthesis of four clusters in the shared fsDNR, thereby cooperatively amplifying the green fluorescence signal for sensitive assay of tI*. Meanwhile, the topological conformation of fsDNR can be stabilized by the as-formed cluster adducts to rivet the pair of two splits in the nicks. Benefitting from the self-enhanced effect of multiple emitters, this label-free fluorescent sensing strategy features simplicity, rapidity, and high on–off contrast, without involving complicated nucleic acid amplifiers.
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Bioactive Materials
·
2025
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IF 20.3
Yuyun Ye,Yan Liu,Shengchao Ma,Xipeng Li,Wei Wang,Xu Chen,Judun Zheng,Zhijin Fan,Yideng Jiang,Yuhui Liao
Infectious wound healing remains a significant medical challenge due to chronic inflammation and bacterial colonization. Effective antimicrobial and anti-inflammatory therapies are essential to facilitate wound recovery. Herein, we introduce a highly biocompatible, ROS-responsive DNA hydrogel (LGAH), modified with aggregation-induced emission luminogens (AIEgen) and incorporating ginseng-derived exosomes (G-Exos) and nitric oxide (NO) donor-L-arginine (L-Arg) to promote healing of infected wounds. The hydrogel degrades in response to elevated ROS levels, releasing therapeutic agents. Upon laser irradiation, AIEgen generates 1 O 2 , which activates L-Arg to produce NO, leading to a synergistic antimicrobial effect. NO is particularly effective at inhibiting bacterial growth and promoting angiogenesis, supporting wound healing. G-Exos modulate immune responses, reduce inflammation, and promote the transition from the inflammatory to the proliferative phase. They also enhance cell proliferation, migration, and collagen production, which are key to tissue regeneration. In vivo experiments demonstrated that LGAH significantly accelerates S. aureus -infected wound healing by modulating the wound microenvironment and promoting tissue regeneration. Transcriptomic analysis revealed that LGAH down-regulates gene expression in inflammation and immune response signaling pathways while up-regulating genes related to energy metabolism. Biosafety evaluations at cellular and animal levels have demonstrated that LGAH possesses excellent biocompatibility and biodegradability, making it ideal for tissue repair and regeneration. This multifunctional DNA hydrogel system offers a safe and promising strategy for the clinical treatment of infected wounds.
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高影响因子
ADVANCED FUNCTIONAL MATERIALS
·
2024
·
IF 18.5
Tiantian Xue,Hongyan Wei,Fenfang Li,Yixin Zhang,Yuanyuan Jin,Yanteng Xu,Hon Fai Chan,Yingying Xu,Yin-Xiong Li,Mingqiang Li,Yu Tao
Acute liver failure (ALF) involves extensive necrosis of liver cells and severe impairment of liver function. Hepatocyte transplantation holds promise for treating ALF by swiftly supporting liver functions and promoting liver regeneration. However, the scarcity of suitable cell sources requires strategies to obtain enough functional hepatocyte-like cells (HLCs) and optimize their in vivo transplantation efficiency. A DNA hexahedral nanostructure (DHN) is developed loaded with microRNA-122 to efficiently induce hepatic differentiation of human adipose-derived mesenchymal stem cells into HLCs. These HLCs can serve as alternative hepatocyte sources, as confirmed by expression of liver-specific genes and proteins, and the restoration of liver functions. To enhance in vivo survival efficiency of HLCs, a versatile scaffold is also created by 3D printing the calcium-cross-linked mixture bioink composed of sodium alginate, gelatin, and silk fibroin with excellent ROS scavenging capabilities. The scaffold is infused with chitosan-DHN hydrogel containing HLCs for tissue engineering orthotopic transplantation in CCl 4 -induced ALF mice. The transplanted composite scaffold-HLCs successfully repair tissue necrosis in the liver injury area of mice and regulate expressions of genes and proteins associated with inflammation, oxidative stress, and hepatocyte function. Collectively, this study offers a novel approach and strategy for identifying alternative hepatocyte sources and treating ALF.
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高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2024
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IF 4.3
Dong Zhang,Ping Yan,Hong Yu,Jing Sun,Shuyun Zhu,Xian-En Zhao
Development of accurate, convenient and portable methods for monitoring 4-aminophenol (4-AP) is extremely important because of its strong toxicity. Here, a ratiometric fluorescence sensor based on Ag + -enhanced luminescence of Tb-DNA complexes has been presented for the detection of 4-AP. The luminescence of Tb-DNA complexes is enhanced about 30 times by Ag + , which can trigger energy transfer from DNA to Tb 3+ more efficiently. In the presence of 4-AP, Ag + can be reduced into Ag 0 owing to its strong reducibility, inducing the decrease of Tb-DNA complexes at 545 nm remarkably. Besides, 4-AP exhibits intrinsic fluorescence at 375 nm under the same conditions. Therefore, ratiometric detection of 4-AP can be achieved using F 375 /F 545 as readout with a detection limit of 0.4 μM. Real water samples have been tsted to evaluate this method in practical application and satisfactory results have been obtained. Furthermore, the addition of 4-AP into Tb-DNA-Ag + system induces a visible color variation from green to bluish violet, enabling visual detection of 4-AP under the assistance of a smartphone.
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高影响因子
TALANTA
·
2024
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IF 5.6
Meixiang Xue,Shuangxi Cai,Ye Deng,Fang Luo,Jianhui Huang,Zhenyu Lin
T-2 toxin, a hazardous mycotoxin often present in cereals and products based on cereals, poses a substantial risk to humans and animals due to its high toxicity. The development of uncomplicated, quick and highly sensitive methods for detecting T-2 toxin is imperative. In this work, a portable sensing system was constructed using water column height as a readout device in combination with a controlled release system, which allows for an accurate quantitative analysis of T-2 toxin without the need for expensive instrumentation or skilled technicians. Hyaluronic acid (HA) hydrogel was constructed by double cross-linked DNA/aptamer hybrids with polyethyleneimine (PEI) and embedded with platinum nanoparticles (Pt NPs). The aptamer specifically bound to T-2 toxin in its presence, resulting in the disruption of the hydrogel and subsequent release of the Pt NPs. These Pt NPs were later mixed with a solution of H 2 O 2 in a confined reaction flask, leading to the decomposition of H 2 O 2 into O 2 . A glass capillary tube containing a column of red water had been inserted into the cap of the reaction flask, and the low solubility of O 2 led to an increase in pressure within the reaction unit, causing the red water column to rise. There is a good linear correlation between the height of the capillary liquid level and the T-2 toxin concentration in the range of 20 ng/mL to 6 μg/mL. The system has been successfully used to detect T-2 toxin in samples of barley tea and corn.
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高影响因子
Journal of Food Measurement and Characterization
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2024
·
IF 2.9
Meng Wenya,Xue Yuhan,Zhang Jing,Wang Ye,Hou Hu,Li Jing,Dong Ping
Fish sperm extracts have been shown to have various activities, but it has not been effectively developed and utilized at present due to the lack of effective methods for preparing edible grade products. This study proposed a method for preparing edible fish sperm DNA from Alaska pollock (PSD) and evaluated the hepatoprotective effect of the extracted DNA. Firstly, the preparation conditions of fish sperm DNA were optimized by response surface methodology. Under the ideal conditions that the ratio of solid to liquid was 3:1, the pH of extractant was 7.5, the purified solvent was saturated sodium carbonate solution and absolute ethanol was twice the volume of purified solvent, the yield of PSD was (13.657 ± 0.577) µg/mg. To evaluate the liver protective effects of the extracted DNA, the digestion products by three digestion enzymes (pepsin, DNase I and DNase II) compared using an alcohol-induced HepG2 cell model. The DNase I hydrolysis product was more effective in preventing cell alcohol damage, as shown by reducing the content of lipid peroxides. Transcriptomics and metabolomics data revealed that the DNase I hydrolysis product activated the Nrf2/HO-1 pathway through the PI3K/Akt signaling pathway and regulated abnormal lipid synthesis through the steroidogenic pathway. This study will provide an important basis for the evaluation and analysis of the hepatoprotective effect of fish sperm DNA in vivo. Overall, our findings will promote the comprehensive utilization of fish sperm and other aquatic wastes, and provide scientific guidance for the development of functional nucleic acid foods.
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PNAS Nexus
·
2025
·Vol. 4
·期 5
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IF 3.8
Sun Kai,Shi Zeyu,Dai Lingzhi,Si Youbin,Ma Junchao,Lin Hui,Yu Han-Qing
Endocrine-disrupting chemicals (EDCs), such as 17β-estradiol (E2) and bisphenol A (BPA), can induce DNA damage, leading to genomic instability and cell death. Laccase, an enzyme secreted by diverse organisms, plays a critical role in mitigating the cytotoxicity of these contaminants. Despite its importance, the dynamic evolution and interaction mechanisms of EDCs and DNA in laccase catalysis remain poorly understood. This study investigates the interactions between EDCs and DNA during laccase-induced polymerization transfer at a molecular level. As the DNA concentration was increased from 0 to 7.575 nM, the pseudo-first-order kinetic constants for E2 and BPA decreased by 2.03 and 2.10 times, respectively. DNA-bound EDCs disrupted the catalytic activity and stability of laccase, thereby delaying the polymerization transfer rate of EDCs. E2 and BPA bound to DNA base pairs via groove and intercalative modes, respectively. Laccase-induced polymerization reduced damage to the DNA helix and base stacking caused by EDC binding. Moreover, the resulting DNA–EDC-precipitated polymers, formed through continuous laccase polymerization, exhibited denser and more complex structures compared with spherical EDC-precipitated polymers, confirming DNA encapsulation and/or binding. This work underscores the intramolecular mechanisms of EDC interaction with DNA in vitro during the laccase-induced polymerization, offering efficient ways to mitigate the genotoxicity of EDCs.Endocrine-disrupting chemicals (EDCs) are often described as “a ticking time bomb threatening human survival” (1). Globally, the widespread presence of both natural and synthetic EDCs, such as 17β-estradiol (E2) and bisphenol A (BPA), has raised significant concerns about their detrimental effects on wildlife and human health (2, 3). Due to their persistent and bioaccumulative nature, EDCs represent a latent crisis for both environmental and human health. Moreover, these chemicals undergo transformations in the environment to form secondary pollutants, which are often more toxic than their precursors (4). These compounds, entering organisms directly or indirectly, have been linked to reproductive disorders, deformities in sexual organs, sex reversal, and feminization in wildlife species (5). Recent studies also correlate the exposure to EDCs with increasing rates of large-bowel, breast, cervical, and ovarian cancers in women and declining sperm count and motility in men (6, 7).The hazardous effects of EDCs are attributed to their interactions with DNA, disrupting DNA repair, replication, and transcription processes, and thereby causing enhanced DNA damage and cell death (8, 9). Understanding the dynamic processes and intermolecular interactions of EDCs with DNA is crucial for elucidating their mechanisms of genotoxicity.DNA, the carrier and transmitter of hereditary information in nearly all living systems, plays a central role in vital biogenetic processes, such as gene expression, transcription, mutation, and carcinogenesis (10). Composed of pentose sugar, phosphoric acid, and nitrogenous bases, DNA's genetic information is encoded by specific sequences of these bases. The stability of the DNA helix is significantly maintained by the stacking and hydrogen-bonding interactions between nucleobases (11). Thus, the interaction of EDCs with DNA could directly impact its structure and function, leading to DNA damage in exposed cells and altering its existing functions (1). Organic pollutants of biological importance are known to interact with DNA through noncovalent interactions, including electrostatic interactions, groove binding, and intercalative binding (12–14).Laccase (EC 1.10.3.2, oxygen oxidoreductase), a member of the multicopper oxidase superfamily, is naturally secreted by a variety of organisms such as bacteria, fungi, plants, and insects. It has garnered attention for its high activity, low energy requirements, and nontoxicity in degrading harmful phenolic substances (15, 16). Laccase catalyzes the oxidation of EDCs, facilitating the formation of phenoxy radicals, which subsequently polymerize into dimers, trimers, tetramers, oligomers, and polymers (17, 18). Despite its potential, the detailed understanding of the dynamic evolution and molecular mechanisms of interaction between EDCs and DNA during laccase-induced polymerization remains scant.This work aims to elucidate, at the molecular level, the dynamic processes and interaction mechanisms between EDCs and DNA during the laccase-induced polymerization transfer. We explored the reaction kinetics of EDCs under varying DNA concentrations using a pseudo-first-order kinetic model and utilized high-resolution mass spectrometry (HRMS) to identify key oxidation products. Advanced spectroscopic techniques, such as UV-Vis spectroscopy, attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), and circular dichroism (CD) spectroscopy, were employed to reveal the dynamic interactions of DNA with EDCs during polymerization. Atomic force microscopy (AFM) was used to unmask the dynamic variations in DNA morphology on interaction with EDCs and their oligomers from the molecular perspective. Further, the precipitated polymers were characterized using scanning electron microscopy (SEM) equipped with an energy-dispersive X-ray spectrometer (EDS), FTIR, and 13C-nuclear magnetic resonance spectroscopy (13C-NMR). Molecular dynamics simulation (MDS) was conducted to verify the intermolecular interactions between DNA and the oligomers of EDCs. The cytotoxicity of DNA–EDC solutions treated by laccase-induced polymerization was evaluated over time. By uncovering the dynamic evolution and intermolecular interactions of EDCs and DNA in vitro during the laccase-induced polymerization, this study offers insights into molecular strategies for mitigating the genotoxicity of EDCs.Increasing DNA concentrations significantly impeded the laccase-induced single-electron oxidation transfer of EDCs. Figure S1 illustrates that the oxidation rates of E2 and BPA decreased from 97.25 to 80.37% and 71.64 to 54.18%, respectively, after a 3-h reaction, as the DNA concentration was increased from 0 to 7.575 nM. The laccase-mediated oxidation of EDCs adhered to a pseudo-first-order kinetics model within 1 h, with k1 values for E2 and BPA decreasing by factors of 2.03 and 2.10, respectively, as the DNA concentration was increased (R2 = 0.96–0.99). This suggests that laccase activity was inversely related to the DNA concentration during the enzyme-catalyzed oxidation of EDCs (Fig. S2). Linear regression analysis further elucidated the dependency of the k1 value on low DNA concentration (0–0.7575 nM), revealing a linear relationship (R2 ≥ 0.98) and calculated pseudo-second-order rate coefficients (k2) for E2 and BPA of 1.52 and 0.33 nM−1·h−1, respectively (Fig. 1a and b).High levels of phenoxy radicals, produced by the laccase-induced oxidation of EDCs, facilitated the polymerization transfer. HRMS identified the polymerization products, revealing their molecular architectures through computational analysis (Table S1 and Fig. 1c). Notably, three major E2 oligomers—dimer (m/z = 541.3310), trimer (m/z = 811.4930), and tetramer (m/z = 1,081.6555)—suggested the pattern of n × M − 2(n − 1) for EDC polymerization products, where n is the number of polymerized EDC monomers and M is the molecular mass of the monomer. Additionally, a peak at m/z = 269.1548 indicated the formation of estrone (E1) by deprotonation, accounting for <2.4% of the initial E2 after 1 h of reaction. This pattern was consistent with the laccase-induced polymerization of BPA, suggesting that polymerization transfer is the predominant pathway in EDC oxidation by laccase, regardless of the presence of DNA.UV-Vis absorption spectroscopy confirmed the interaction modes between DNA and EDCs. The UV-Vis absorption spectra of DNA displayed two peaks at 234 and 260 nm (Fig. S3). The addition of E2 resulted in a hyperchromic effect at 260 nm, indicating damage to the DNA helix through a nonintercalative interaction mode. The degree of E2 polymerization transfer correlated negatively with the intensities of the characteristic DNA peaks (Fig. 2a). In contrast, the interaction with BPA showed a hypochromic effect, suggesting an intercalative binding that involves strong π–π aromatic stacking interactions between BPA and the phosphate backbone of the DNA helix (19). The degree of BPA polymerization transfer correlated positively with DNA peak intensities (Fig. 2b). Clearly, laccase-induced polymerization effectively reduced the concentration of EDCs and mitigated their interaction with DNA.The molecular fingerprint of DNA is located in the spectral region of 1,800–700 cm−1 due to nitrogenous bases, phosphate, and deoxyribose stretching vibrations. Binding of EDCs to DNA bases was investigated by analyzing spectral changes at 1,691, 1,648, 1,605, and 1,485 cm−1 that were attributed to guanine, thymine, adenine, and cytosine base vibrations, respectively. FTIR spectra explored the binding sites of DNA and EDCs, with characteristic DNA peaks indicating interactions at thymine and adenine bases, which appeared to be primary binding sites for EDCs (Fig. 2c and d). CD spectroscopy further revealed conformational changes in DNA induced by EDCs, highlighting the distinct interaction modes of E2 and BPA with DNA. The upward shift in the positive peak suggested enhanced base stacking due to groove binding by E2, while the downward shift in the negative peak for BPA indicated intercalative binding (Fig. 2e and f).AFM does not require any additional sample pretreatment to observe samples in liquids, making it exceptionally suitable for DNA imaging and therefore plays an important role in probing the intermolecular interactions of EDCs and DNA during the laccase-induced polymerization. AFM offered direct evidence of DNA binding with EDCs at the molecular level (Fig. 3). No obvious change in the contour length of DNA was observed in the presence of E2, confirming that E2 bound to DNA by groove mode (Fig. 3a). However, the interaction of intercalating BPA with DNA could lead to an increase in the contour length of DNA by bridging two or more DNA molecules (Fig. 3e). Further, the enhanced degree of EDC polymerization boosted DNA encapsulation and/or binding, forming larger spherical particles (Fig. 3b–d and f–h).SEM analysis showed that compared with the spherical E2-precipitated polymers, DNA–E2-precipitated polymers displayed a denser and thicker morphology, indicative of tighter and more complex structural integration (Fig. 4a and b). EDS confirmed a lower carbon-to-oxygen ratio in the DNA–E2-precipitated polymers compared with those without DNA, suggesting more extensive oxygen bonding. A similar phenomenon was also found in the BPA and DNA–BPA-precipitated polymers (Fig. 4e and f). As demonstrated in Fig. 4c and g, the EDC-precipitated polymers displayed the functional characteristics of the aromatic skeleton, phenolic –OH, and ether linkage. By comparison, the intensities and positions of the above functional groups in the DNA–EDC-precipitated polymers changed unmistakably. 13C-NMR spectra of the precipitated polymers revealed a predominance of aromatic and phenolic carbon, indicating that DNA was potentially encapsulated and/or bound to the EDC-precipitated polymers during the laccase-induced polymerization and thus facilitated more complex carbon backbone formations (Fig. 4d and h).The dynamics of polymerization and the molecular interactions were extensively analyzed to elucidate the complex behavior of EDCs in the presence of DNA during laccase catalysis. These insights provide a deeper understanding of the intramolecular mechanisms through which laccase-mediated processes may mitigate the genotoxicity of EDCs, highlighting the potential applications of laccase polymerization for the decontamination and detoxification of EDCs at the molecular level.To support the above experimental results, we further explored the stability and position changes of EDCs and their oligomers binding to DNA by computer-aided MDS. Root-mean-square deviation (rmsd) serves as a measure of the stability and interaction between DNA and substrates. Higher rmsd values suggest more unstable interactions. In this study, the interactions of DNA with EDCs and their oligomers (dimer, trimer, and tetramer) were examined over a 100-ns MDS period. As illustrated in Fig. 5a–e, rmsd values for DNA-bound E2 and its oligomers ranged from 0 to 7.0 Å. The average rmsd for DNA-bound E2 was 1.05 Å, indicating more stable interactions compared with DNA-bound E2 dimer (2.68 Å), trimer (1.73 Å), and tetramer (2.10 Å). Hydrogen bonds, crucial for the affinity and selectivity of the DNA-substrate complex, diminished in number from the monomer to the oligomers, underscoring the enhanced stability of DNA-bound E2. Conversely, for BPA, the mean rmsd values increased with oligomerization; DNA-bound BPA monomer exhibited an rmsd of 3.06 Å, greater than its oligomers—dimer (1.74 Å), trimer (2.45 Å), and tetramer (2.44 Å; Fig. 5f–j), correlating with an increase in hydrogen bonds with higher molecular weights, indicating greater stability in DNA-bound BPA oligomers.As mentioned above, hydroxyl substitution facilitated the binding of EDCs and their oligomers to DNA, but the intermolecular binding was relatively unstable (rmsd > 1). Figure 6 shows the position changes of EDCs and their dimers, trimers, and tetramers relative to DNA at different simulation times. As the MDS time was increased, EDCs and their oligomers gradually deviated from the initial binding sites of DNA. Furthermore, these results also disclosed abnormal DNA structures, which were consistent with the CD spectroscopy. Overall, the MDS results confirm that EDCs and their oligomers unstably bound to their corresponding binding sites during the simulation process.The dynamic interactions and mechanisms of DNA with EDCs during the laccase-induced polymerization remain poorly understood. Laccase facilitates the one-electron oxidation of EDCs, predominantly leading to polymerization products, while DNA hampers this transfer by interacting with functional groups of DNA molecules, such as base pairs and phosphate skeletons. This interaction forms complexes of DNA-bound EDCs, which obstruct laccase's catalytic activity and stability, thereby slowing the polymerization rate of EDCs. In contrast, the polymerization products of EDCs, also bound to DNA via hydrogen bonds, form denser and thicker structures compared with those without DNA, suggesting potential encapsulation and/or binding within the DNA–EDC polymers. Understanding these dynamic processes and interactions provides insights into mitigating the genotoxicity and cancer risks associated with EDCs.The EDC polymers precipitated through laccase-induced polymerization play a crucial role in reducing the cytotoxic effects of EDCs (20). The phytotoxicity assessments of DNA–EDC solutions treated through laccase-induced polymerization, illustrated in Fig. S4, demonstrate significant reductions in EDC-induced inhibitory effects on seed germination and root elongation. For instance, the germination index (GI) of wheat seeds treated with E2 increased from 12.85% (severe inhibition) to 87.48% (no inhibition) over a 9-h laccase polymerization period. The addition of DNA maintained a GI of 57.69%, even after 9 h. Furthermore, the cytotoxicity of polymerization products diminished over time, showcasing the potential of laccase-induced polymerization in alleviating the genotoxic effects of EDCs. Significantly, microbial enzymes may degrade DNA, resulting in the release of DNA-bound EDCs. Future studies are required to explore the stability of DNA-bound EDCs and their oligomers, as well as the long-term effects of the complexes in the environment. Furthermore, the in vivo interactions of DNA with EDCs should also be explored to uncover the self-detoxification mechanisms of laccase-producing organisms at a genomic level.In summary, this work provides comprehensive insights into the complex interactions between EDCs and DNA in the context of laccase-mediated reactions. The findings reveal that DNA significantly alters the kinetics and mechanisms of EDC polymerization, potentially offering a novel approach to mitigate the environmental impact and genotoxicity of these harmful compounds. By elucidating the specific binding interactions and the resulting structural changes in DNA and EDC polymers, this research contributes to a deeper understanding of the intramolecular mechanisms of EDC interaction with DNA in vitro during the laccase-induced polymerization and opens new avenues for the development of more effective decontamination and detoxification strategies in vivo.E2 (C18H24O2, ≥98%), BPA (C15H16O2, ≥99%), double-stranded salmon testes DNA (%G-C content: 41.2%; molecular mass: 1.3 × 106 Da; DNA fragment lengths: ∼2,000 bp), and Trametes versicolor laccase (light brown, ≥0.5 U·mg−1) were sourced from Sigma-Aldrich Co., China. Methanol (CH3OH, suitable for high-performance liquid chromatography [HPLC], ≥99.9%) and acetonitrile (CH3CN, suitable for HPLC, ≥99.9%) were procured from Thermo Fisher Scientific Inc., USA. Tris-HCl buffer solution (10 mM, pH 7), citrate-phosphate buffer solution (CPBS, 10 mM), and Murashige and Skoog (MS) medium were obtained from Aladdin Chemistry Co., China. Stock solutions of E2 and BPA were prepared in methanol at 1 mM. Laccase stock solution (100 U·mL−1) and DNA stock solution (dissolving 75.75 nmol of DNA in 100 mL Tris-HCl buffer) were prepared in Milli-Q water. UV absorption at 260 nm with a molar extinction coefficient (ε260) of 6,600 L·mol−1·cm−1 was used to determine the DNA concentration in the solution. The DNA purity, indicated by an absorbance ratio at 260 and 280 nm (A260/A280) of >1.83, confirmed high purity. Wheat seeds (Triticum aestivum L.) were supplied by the Anhui Academy of Agriculture Sciences, China. All solutions were prepared using Milli-Q water (18.25 MΩ·cm) and stored at 4 °C prior to use.The reaction kinetics of EDCs catalyzed by laccase in the presence of DNA were conducted in 20 mL of CPBS at 25 ± 0.5 °C and pH 5 under dark conditions. A concentration of 0.5 U·mL−1 laccase was added to solutions containing 5 μM of either E2 or BPA and varying concentrations of DNA (0–7.575 nM). Periodically, 0.5 mL samples were extracted from the reaction mixture, quenched immediately with an equivalent volume of methanol, and filtered through a 0.22-μm membrane for analysis. Experiments were replicated in triplicate, and the oxidation kinetics of EDCs were modeled by pseudo-first-order kinetics:where k1 is the pseudo-first-order rate constant and [EDCs] is the residual concentration of free EDCs in the reaction system at a given time.Details on the determination of laccase activity are provided in the Supporting Information.Quantitative and qualitative analyses, including HPLC and HRMS, are described in the Supporting Information.The interaction mode between DNA and EDCs during enzymatic catalysis was examined using a UV-Vis spectrophotometer (UV-2550, Shimadzu Co., Japan) equipped with 1 cm quartz cuvettes. Samples were analyzed at preset intervals (0, 5, 10, 15, 30, 45, 60, 90, 120, 150, and 180 min) for UV absorption spectrum (220–300 nm) in 1-nm increments at 25 ± 0.5 °C. ATR-FTIR spectroscopy (NEXUS-870, Thermo Nicolet Co., USA) and CD spectroscopy (Chirascan, APL, UK) were also employed to further explore the binding mechanism between DNA and EDCs.The morphological changes of DNA binding to EDCs and their oligomers were directly observed by AFM. DNA (7.575 nM) and EDCs (5 μM) were incubated at 25 ± 0.5 ° C and pH 5.0 to ensure that EDCs were adequately bound to DNA. Next, the enzymatic reaction was initiated by adding 0.5 U·mL−1 laccase to the mixture. By adjusting the pH of the mixture to 1.5, the enzymatic reaction was periodically terminated. To prepare the sample for AFM, 50 μL of the mixed solution was pipetted onto freshly cracked mica sheets, gently washed with ultrapure water and air-dried, and then imaged by AFM (Dimension Icon, Bruker Co., USA). AFM images were recorded at a resolution of 500 × 500 pixels and a scanning line speed of 0.600–0.998 Hz.Precipitated polymers collected from the laccase-induced polymerization transfer of EDCs were freeze-dried, ground, and sieved. Their microstructures, functional groups, and chemical compositions were characterized using SEM (Regulus 8100, Hitachi, Japan) equipped with an EDS (Bruker Co., Germany), FTIR, and 13C-NMR (Avance III, Bruker Co., Germany).MDS was performed to model the interaction of DNA with EDCs and their oligomers (dimer, trimer, and tetramer). The 3D structure of B-DNA dodecamer d(CGCGAATTCGCG)2 was sourced from the Protein Data Bank (PDB ID: 2B0 K). The structures of EDCs and their oligomers were built using ChemBioDraw Ultra 14.0, optimized with ChemBio3D Ultra 14.0, with nonpolar hydrogen atoms merged and Kollman charges added using MGLTools 1.5.6. Simulations were conducted using GROMACS 2016.4 with the AMBER99SB force field. Rmsd was calculated to assess the stability of each complex:where Natm is the number of atoms, rA is the position of atom A, and rAref is the reference position of atom A.The phytotoxicity of DNA and EDC solutions treated by laccase-induced polymerization was evaluated using a GI. Wheat seeds were monitored over a 3-day cultivation period in MS medium under controlled conditions. The GI was calculated using the formula:where NCRS and NMW are the number of seeds germinated in the reaction solution and Milli-Q water, respectively, and RCRS and RMW are the root lengths in the reaction solution and Milli-Q water, respectively.Supplementary material is available at PNAS Nexus online.This work was financially supported by the National Natural Science Foundation of China (42277019 and 51821006) and the Natural Science Foundation-Excellent Youth Fund Project of Anhui Province, China (2308085Y28).K.S., Z.S., and J.M. were involved in data curation and formal analysis. L.D. was involved in formal analysis. Y.S. was involved in software, validation, and writing—review and editing. H.L. was involved in software and validation. H.-Q.Y. was involved in conceptualization, resources, supervision, funding acquisition, writing—original draft, project administration, and writing—review and editing.All data are included in the article and Supporting Information.
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CHEMISTRY-A EUROPEAN JOURNAL
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2025
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IF 3.7
Fa Wang,Zhiyang Wang,Shuqi Huang,Jinrong Yang,Yu Chen,Hui Chao
Graphical A convenient strategy by synergistic delivering DNA and DNA photocleavage agents to tumor cells was developed for effective photodynamic immunotherapy under hypoxia. Plasmid DNAs intercalated with Ru(II) complexes were encapsulated in liposomes to create nano-photosensitizers. Upon light exposure, the ruthenium complex photo-cleavages DNA. The DNA fragments specifically stimulate the cGAS-STING pathway and induce immunogenic death. This study presents a convenient strategy for photodynamic immunotherapy against cisplatin-resistant tumor cells under hypoxia.
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
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2025
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IF 3.8
Lai Shanshan,Guo Jiahong,Li Xin,Yu Xiaoxiao,Lai Guosong
Fluorescence biosensors hold significant importance for testing antibiotic residues which seriously endanger public health. However, how to adopt appropriate strategies to address the false result disadvantage involved in traditional single-channel biosensors is still a great challenge. Meanwhile, too much attention focused on designing signal amplification strategies of biosensors unavoidably decreases their detection efficiency. Herein, we combined the designed dual DNA recycling amplification strategy with CRISPR/Cas12a-mediated dual-channel signal output mode to successfully develop a novel ratiometric fluorescence biosensor for testing kanamycin (Kana) residues in complex sample matrices. The first recycling was formed from an exonuclease-assisted aptamer recognition reaction, which also triggered another cascade DNA recycling to amplify the release of the Cas12a activator. With the non-discrimination cleavage of Cas12a to cause reverse fluorescence changes of copper nanoclusters and an AMAC-labeled signal DNA, the ratiometric signal transduction strategy was constructed. Under optimal conditions, this biosensor could be applied for ultrasensitive testing of Kana antibiotics in a five-order of magnitude wide linear range with a low detection limit of 17.2 fg mL −1 . Benefiting from the self-correction function of the ratiometric signal transduction mode, it showed promising practicality in lake water and milk samples with the relative error less than 4.9% to the standard ELISA results. Besides CRISPR/Cas12a-based fluorescence output efficiency improvement, this biosensor also excluded the complicated manipulations and expensive instruments required in traditional methods. Therefore, it provides a good choice for expanding the application of fluorescence biosensing technology for practical analysis application. Graphical
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