Henningsenwilliamson5389

Uracil-DNA glycosylase (UDG) is essential to the maintenance of genomic integrity due to its critical role in base excision repair pathway. However, existing UDG assays suffer from laborious procedures, poor specificity, and limited sensitivity. In this research, we construct a catalytic single-molecule Föster resonance energy transfer (FRET) biosensor for in vitro and in vivo biosensing of UDG activity. Target UDG can remove uracil base from the detection probe and cause the cleavage of detection probe by apurinic/apyrimidinic endonuclease (APE1), which exposes its toehold domain and initiates catalytic assembly of two fluorescently labeled hairpin probes via toehold-meditated strand displacement reaction (SDA) to generate abundant DNA duplexes with amplified FRET signal. In this assay, target UDG signal is amplified via enzyme-free catalytic reaction and the whole reaction may be completed in one step, which greatly simplifies the assay procedure, reduces the assay time, and facilitates the cellular imaging. This biosensor enables specific and sensitive measurement of UDG down to 0.00029 U/mL, and it is suitable for analyzing kinetic parameters, screening inhibitors, and even imaging endogenous UDG in live cells. Importantly, this biosensor can visually quantify various DNA repair enzymes by rationally altering DNA substrates.In this study, a signal-on type PEC immunosensor was constructed to detect neuron-specific enolase (NSE) via Z-scheme WO3/NiCo2O4 p-n heterojunction with cactus-like structure used as photoactive materials and MnxCd1-xS⊃Au NPs (MCS⊃Au NPs) as signal labels. Firstly, Z-scheme WO3/NiCo2O4 heterojunction could accelerate the separation efficiency of carriers and well-matched photoactive materials may promote charge migration, which resulted in WO3/NiCo2O4 generating strong and stable current. ZCL278 supplier In addition, Z-scheme WO3/NiCo2O4 heterojunction directly grown on the surface of FTO via hydrothermal method facilitated the preparation of PEC immunosensor with outstanding stability. Secondly, an efficient signal amplification strategy was proposed by MnxCd1-xS⊃Au NPs incubating with signal antibody (Ab2). On the one hand, the well-matched energy levels of MnxCd1-xS with WO3/NiCo2O4 boosted the photo-generated electrons transferred to the electrode; on the other hand, the LSPR effect of Au may convert thermion to photocurrent to achieve signal amplification. Based on the above strategies, a PEC immunosensor with outstanding reproducibility and stability was obtained for sensitive detection of NSE. Under the optimum experimental conditions, current response range of the constructed signal amplification PEC sensor to NSE was 0.1 pg/mL ∼50 ng/mL and the detection limit was 0.07 pg/mL (S/N = 3). After the application tests in the detection of actual samples, the feasibility of the prepared PEC immunosensor with excellent selectivity, high sensitivity and satisfactory reproducibility was verified and the satisfactory results were obtained.Despite its high potential, PD-L1 expressed by tumors has not been successfully utilized as a biomarker for estimating treatment responses to immunotherapy. Circulating tumor cells (CTCs) and tumor-derived exosomes that express PD-L1 can potentially be used as biomarkers; however, currently available assays lack clinically significant sensitivity and specificity. Here, a novel peptide-based capture surface is developed to effectively isolate PD-L1-expressing CTCs and exosomes from human blood. For the effective targeting of PD-L1, this study integrates peptide engineering strategies to enhance the binding strength and specificity of a β-hairpin peptide derived from PD-1 (pPD-1). Specifically, this study examines the effect of poly(ethylene glycol) spacers, the secondary peptide structure, and modification of peptide sequences (e.g., removal of biologically redundant amino acid residues) on capture efficiency. The optimized pPD-1 configuration captures PD-L1-expressing tumor cells and tumor-derived exosomes with 1.5-fold (p = 0.016) and 1.2-fold (p = 0.037) higher efficiencies, respectively, than their whole antibody counterpart (aPD-L1). This enhanced efficiency is translated into more clinically significant detection of CTCs (1.9-fold increase; p = 0.035) and exosomes (1.5-fold increase; p = 0.047) from patients' baseline samples, demonstrating stronger correlation with patients' treatment responses. Additionally, we confirmed that the clinical accuracy of our system can be further improved by co-analyzing the two biomarkers (bimodal CTC/exosome analysis). These data demonstrate that pPD-1-based capture is a promising approach for capturing PD-L1-expressing CTCs and exosomes, which can be used as a reliable biomarker for cancer immunotherapy.Visual lateral flow immunoassays (LFA) have been recognized as the attractive point-of-care testing (POCT) for bioanalysis; however, they have been constrained by insufficient sensitivity and limited reliability. Herein, combining the catalytic sites of Cu nanoparticles with an inherent photothermal polydopamine (PDA) scaffold via a one-step process, a compact Cu-anchored PDA (PCu) was engineered as the efficient signal element for the multimodal LFA (mLFA). The robust PCu with peroxidase-mimics and photothermal properties, could simultaneously provide triple signal readouts for colorimetric, amplified colorimetric and photothermal detection toward Aspergillus flavus (A. flavus). Attractively, the multiple guaranteed detection of PCu-based mLFA enabled the accurate and sensitive detection of A. flavus mycelium biomass, down to 0.45 and 0.22 ng mL-1, which was 19- and 40-fold improvements compared to traditional colorimetry. Besides, mLFA was successfully applied to actual samples with satisfactory recoveries from 89.9 to 109%, indicating the highly reliable analytical performance. This work paved a prospective way for the construction of efficient peroxidase-mimics and superior photothermal multifunctional nanomaterials, providing a potential versatile visual POCT platform for analytical events.The emerging field of cultured meat faces several technical hurdles, including the scale-up production of quality muscle and adipose progenitor cells, and the differentiation and bioengineering of these cellular materials into large, meat-like tissue. Here, we present edible, 3D porous gelatin micro-carriers (PoGelat-MCs), as efficient cell expansion scaffolds, as well as modular tissue-engineering building blocks for lab-grown meat. PoGelat-MC culture in spinner flasks, not only facilitated the scalable expansion of porcine skeletal muscle satellite cells and murine myoblasts, but also triggered their spontaneous myogenesis, in the absence of myogenic reagents. Using 3D-printed mold and transglutaminase, we bio-assembled pork muscle micro-tissues into centimeter-scale meatballs, which exhibited similar mechanical property and higher protein content compared to conventional ground pork meatballs. PoGelat-MCs also supported the expansion and differentiation of 3T3L1 murine pre-adipocytes into mature adipose micro-tissues, which could be used as modular assembly unit for engineered fat-containing meat products. Together, our results highlight PoGelat-MCs, in combination with dynamic bioreactors, as a scalable culture system to produce large quantity of highly-viable muscle and fat micro-tissues, which could be further bio-assembled into ground meat analogues.Memory disorders are a common consequence of cerebrovascular accident (CVA). However, uncertainties remain about the exact anatomical correlates of memory impairment and the material-specific lateralization of memory function in the brain. We used lesion-symptom mapping (LSM) in patients with first-time CVA to identify which brain structures are pivotal for verbal and nonverbal memory and to re-examine whether verbal and nonverbal memory functions are lateralized processes in the brain. The cognitive performance of a relatively large cohort of 114 patients in five classic episodic memory tests was analysed with factor analysis. Two factors were extracted that distinguished the verbal and nonverbal components of these memory tests, and their scores were subsequently tested for anatomical correlates by combining univariate and multivariate LSM. LSM analysis revealed for the verbal factor exclusively left-hemispheric insular, subcortical and adjacent white matter regions and for the nonverbal factor exclusively right-hemispheric temporal, occipital, insular, subcortical and adjacent white matter structures. These results corroborate the long-standing hypothesis of a material-specific lateralization of memory function in the brain and confirm a robust association between right temporal lobe lesions and nonverbal memory dysfunction. The right-hemispheric correlates for the nonverbal aspects of episodic memory include not only classic memory structures in the medial temporal lobe but also a more distributed network that includes cortical and subcortical structures also known for implicit memory processes.

Graphene-based microparticles materials are broadly utilized in all sorts of fields owing to their outstanding properties. Despite great progress, the present graphene microparticles still face challenges in the aspects of size uniformity, motion flexibility, and tailorable surface chemistry, which limit their application in some specific fields, such as versatile adsorption. Hence, the development of novel graphene microparticles with the aforementioned characteristics is urgently required.

We presented a simple microfluidic electrospray strategy to generate magnetic Janus reduced graphene oxide/carbon (rGO/C) composite microspheres with a variety of unique features. Specifically, the microfluidic electrospray method endowed the obtaiend microspheres with sufficient size uniformity as well as magnetic responsive motion ability. Additionally, magnetic-mediated surface assembly of phase transition lysozyme (PTL) nanofilm on the microspheres rendered the deposited area hydrophilic while non-deposited area hmicrospheres could serve as adsorbents in a simulative hemoperfusion setup, which further demonstrated the clinical application potential of the magnetic Janus rGO/C microspheres. Thus, we anticipate that the obtained magnetic Janus rGO/C composite microspheres could show multifunctional properties toward water treatment and blood molecule cleaning.

To disperse high concentration of C

fullerene in water, we propose to use an emulsification-evaporation process in the presence of an amphiphilic polymer whose chemical structure has been chosen for inducing specific interaction with fullerene The viscosity enhancement provided by self-assembly of the amphiphilic polymers in water should result in high stability of the suspensions. The organic solvent has also to been chosen so as to maximize the initial fullerene concentration.

The concentrations of polymer and fullerene, the solvent type and the volume fraction of the organic phase have been varied. Their influence on the concentration of the fullerene dispersions and on the size and shape of the resulting nanoparticles have been investigated by UV-Visible spectroscopy, light scattering and cryo-transmission electron microscopy experiments.

The resulting nanoparticles consist of aggregates of C

fullerene stabilized by the cationic polymer with morphologies/sizes tunable through fullerene and polymer concentration.