Probe Technology Research Articles

Warming increases CH4 emissions from rice paddies through shifts in methanogenic and methanotrophic communities

Warming often stimulates methane (CH4) emissions from rice paddies, one of the largest anthropogenic sources of CH4 emissions. However, the responses of methanogenic and methanotrophic communities to warming, particularly within active communities, remain unclear. Therefore, based on a field warming experiment in a rice-wheat system, we investigated the effects of warming on methanogenic and methanotrophic communities, using the DNA stable-isotope probing technology. Our results indicated that warming increased CH4 emissions by 27–49% over two rice growing seasons compared to ambient conditions. Warming significantly increased the abundance of methanogens by 53%, whereas did not affect activities of methanogens and active methanogenic community. Conversely, warming did not influence the abundance of methanotrophs, but reduced activities of methanotrophs by 44%. Notably, warming led to a significant rise in the relative abundance of the active type II methanotrophic community, which exhibits lower CH4 oxidation efficiency. These findings suggest that the observed increase in CH4 emissions under warming conditions is primarily driven by the enhanced abundance of methanogens and the increased presence of less efficient active type II methanotrophs. This study underscores the critical role of active microbial communities in understanding and managing CH4 emissions from rice paddies in a warming world.

Characteristics of organic amendments induce diverse microbial metabolisms for exogenous C turnover in Mollisols

The response of microbial community to organic amendments is closely related to the amendment-derived carbon (C) turnover, which in turn influences the enhancement of soil organic C, including the quantity and quality. The objective of this study was to quantify the decomposition and retention of exogenous C derived from amendments, and to identify the microbial regulatory mechanisms of exogenous C turnover in response to the characteristics of organic amendments. The 13C-labelled glucose, straw and biochar, characterizing organic amendments with high, medium and low labilities, respectively, were used to conduct a 90-day incubation experiment, in conjunction with stable isotope probing technology and amino sugar molecular biomarkers. It was found that the cumulative mineralization of amendment-derived C increased with increasing the corresponding lability of organic amendment, and the decompositions of the added glucose, straw and biochar, expressed as a percentage of the initially added C, were 53.6 %, 37.0 %, and 0.6 %, respectively. Among all treatments, the addition of straw significantly enhanced the total dissolved organic C (DOC) concentration and its ratio to total organic C by increasing the input of exogenous DOC and reducing the decomposition of native soil DOC. The exogenous C use efficiency by microorganisms was significantly enhanced with decreasing the amendment lability, and showed a positive correlation with the total amendment-derived C. However, the microbial growth efficiency was the highest when straw was added, and was closely related to the concentration of amendment-derived DOC. Different functional groups of soil microbes exhibited distinct capacities to metabolize various organic amendments. Generally, the incorporation of amendment-derived C into microbial biomass was significantly affected by fungi and gram-positive (G+) bacteria, while the relative contributions of microbial communities incorporating amendment-derived C into necromass were decreased in the order of gram-negative (G−) bacteria > fungi > actinomycetes > G+ bacteria. From the perspective of microbial metabolism, the larger incorporations of exogenous C into microbial biomass and necromass were observed in the soil with mediumly labile amendment, which contributed to enhance the quantity and quality of organic C in soil. These results would be informative to optimize the organic amendment strategy for integrated soil fertility management.

Synthesis and mechanistic investigation of BPA fluorescent probes targeting BPA for potential application in Boron Neutron Capture Therapy (BNCT)

Boronic acid analogs are crucial in modern organic chemistry and drug development, serving as versatile reagents and intermediates with significant therapeutic applications. This area has gained increased interest with the recent development of the drug 4-boron-L-phenylalanine (L-BPA) for boron neutron capture therapy (BNCT). Fluorescent probe technology offers an essential pathway for imaging drugs in vitro and in vivo, providing high sensitivity with great spatial and temporal resolution for both disease diagnosis and drug development. In this paper, we designed and investigated three fluorescent probes—W-1-NN, W-2-NS and W-3-NO—for sensing 4-boron-L-phenylalanine (L-BPA). Among these, only W-1-NN reacts with L-BPA, resulting in a spectral blue-shift change. This probe can “ratiometrically” and specifically detect L-BPA among various metals, with a limit of detection (LOD) of 7.11 μM. Mechanistic studies revealed that the addition of L-BPA disrupts the inherent ESIPT mechanism of W-1-NN in protonic solutions, resulting in the appearance of a new peak at 372 nm. Additionally, theoretical computational studies have also demonstrated that the complexation of W-1-NN with L-BPA triggers a change in the resonance structure, resulting in a larger energy gap and causing a blue shift in the spectrum. Furthermore, W-1-NN has been successfully applied to the detection of L-BPA in human urine. Therefore, the template probe with N/O as the target and the introduction of N atoms can specifically detect L-BPA. This template probe lays the foundation for the detection of L-BPA, and provides great possibilities for the future realization of the template probe to be connected with different fluorophores to make it emit at long wavelengths to reach the target of the near-infrared.

Azimuthal and radial variations in sap flow and its effects on the estimation of transpiration for Picea mongolica.

In this study, we applied thermal dissipation probe technology to examine sap flow in various directions (east, south, west, and north) and at different depths (0-2, 2-4, 4-6 cm) within the stem of natural Picea mongolica trees in the eastern of Otindag Sandy Land to provide a scientific basis for accurately quantifying water consumption of P. mongolica forests through transpiration and to enhance the understanding of water relations. The results showed that the diurnal variation of sap flow in different directions displayed a unimodal curve, with the sap flow sequence being south>east>west>north. The sap flow at different sapwood depths exhibited an obvious unimodal curve, with a significant decrease as sapwood depth increased. Compared with that calculated from the mean sap flux density in four directions (23.57 kg·d-1), water consumption calculated using the mean value in south-east, east-west, south-west, north-east, north-south, and north-west was overestimated by 10.2%, 5.5%, 14.5%, and underestimated by 12.3%, 8.2%, 9.8%, respectively. The water consumption calculated using the values from the east, south, and west was overestimated by 6.1%, 14.4%, and 15.4%, respectively, and underestimated by 30.7% in the north. In addition, compared with the water consumption calculated from the mean value in three sapwood depths (48.51 kg·d-1), that calculated using sap flux density at sapwood depths of 0-2, 2-4, and 4-6 cm were overestimated by 18.8%, underestimated by 1.7%, and underestimated by 62.9%, respectively. These results indicated that sap flow of P. mongolica had significant azimuthal and radial variations, which considerably influence the estimation of tree water consumption. Installing probes at 0-2 cm simultaneously in both the north and east of the trunk could effectively reduce the estimation error of whole-tree water consumption by 4.2%. This approach enabled the accurate quantification of water consumption of individual P. mongolica trees in sandy areas, thereby improving the precision of transpiration water consumption estimates scaling up from individual level to stand level.

Application of Intelligent Response Fluorescent Probe in Breast Cancer.

As one of the leading cancers threatening women's lives and health, breast cancer is challenging to treat and often irreversible in advanced cases, highlighting the critical importance of early detection and intervention. In recent years, fluorescent probe technology, a revolutionary in vivo imaging tool, has gained attention in medical research for its ability to improve tumor visualization significantly. This review focuses on recent advances in intelligent, responsive fluorescent probes, particularly in the field of breast cancer, which are divided into five categories, near-infrared responsive, fluorescein-labeled, pH-responsive, redox-dependent, and enzyme-triggered fluorescent probes, each of which has a different value for application based on its unique biological response mechanism. In addition, this review also covers the strategy of combining fluorescent probes with various anti-tumor drugs, aiming to reveal the possibility of synergistic effects between the two in breast cancer treatment and provide a solid theoretical platform for the clinical translation of fluorescent probe technology, which is expected to promote the expansion of cancer treatment technology.

Surface plasmon resonance effect cooperated with Z-scheme heterostructure for enhancing photocatalytic nitrogen reduction to ammonia

The photocatalytic efficiency can be improved by constructing a Z-scheme heterojunction, but hindered by the only half utilization efficiency of photogenerated carriers. Thus, a novel material, UiO-66-NH2@TAPB-BTCA-COP-Ag (U6N@COP-Ag), with surface plasmon resonance (SPR) effect synergistic Z-scheme heterostructure has been prepared by depositing Ag nanoparticles (Ag NPs) on TAPB-BTCA-COP (COP)-coated UiO-66-NH2. The deposited Ag NPs expand the range of light absorption and introduce more photogenerated electrons in the composite. The SPR effect of noble metal compensates for the limited utilization of the Z-scheme heterojunction photogenerated carriers and the increased density of semiconductor carriers at the reducing end, which is more conducive to the redox reaction of the catalyst. Without sacrificial agents, U6N@COP-Ag shows great photocatalytic nitrogen reduction conversion efficiency with the rate of NH4+ in ammonia water at 167.63μmol g-1h−1, which is 6.6 and 2.8 times that of the original UiO-66-NH2 and COP, respectively. In-situ XPS and Kelvin probe technology verify that UiO-66-NH2 and Ag nanoparticles provide more photogenerated electrons to COP. The cleavage and conversion of N2 to NH4+ on U6N@COP-Ag was confirmed by the enhancement of NH bonds and NH4+ characteristic absorption peaks in the in-situ diffuse reflectance infrared Fourier transform spectroscopy (in-situ DRIFTS). This work presents a great method to improve the Z-scheme heterojunction photogenerated carrier utilization and the density of semiconductor carriers at the reducing end by the noble metal SPR effect, which is more conducive to enhance the redox reaction of the catalyst.

A Novel Probe Technology for Detecting Native Albumin Activity as a Biomarker in Patients with Hepatitis B-related Cirrhosis and Hepatocellular Carcinoma and Its Clinical Applications

A Novel Probe Technology for Detecting Native Albumin Activity as a Biomarker in Patients with Hepatitis B-related Cirrhosis and Hepatocellular Carcinoma and Its Clinical Applications

The Application of Hydrogen Sulfide Fluorescent Probe in Food Preservation, Detection and Evaluation.

This work primarily reviewed the response mechanism of fluorescent probes for H2S detection in foodstuffs in recent years, as well as the methodologies employed for detecting foodstuffs. Firstly, the significance of studying H2S gas as an important signaling molecule is introduced. Subsequently, a review of the response mechanism of the scientific community on how to detect H2S in foodstuffs samples by fluorescent probe technology is carried out. Secondly, the methods commonly used for detecting foodstuffs samples are discussed, including the test strip method and the spiking recovery methods. Nevertheless, despite the significant advancements in this field, there remain some research gaps. Finally, the article identifies the remaining issues that require further attention in current research and proposes avenues for future investigation. More importantly, this work identifies the current limitations of research in this field and proposes future applications of fluorescent probes for H2S in assessing food freshness and determining food spoilage. Therefore, this review will provide robust technical support for the protection of consumer health and the advancement of the sustainable development of the food industry and also put forward some new ideas and suggestions for future research.

Clinical fluorescence-guide surgery: Tracking leucine aminopeptidase for assisting head and neck squamous cell carcinoma surgery via a near-infrared fluorescent probe

The complete excision of tumors is critical for surgical treatment and the most used for intraoperative margin control method is frozen section analysis (FSA). However, due to its subjective and time-intensive property, there is still a lack of a rapid and effective means to clearly delineate the boundaries between normal and tumor tissues. In this work, we first demonstrated that leucine aminopeptidase (LAP) is highly expressed in clinical head and neck squamous cell carcinoma (HNSCC) and could be used as a biomarker of HNSCC. Based on this, we reported a LAP-activated fluorescent probe, SiR-LAP, and showed its effectiveness in identifying HNSCC. Importantly, we also demonstrated that the fluorescence imaging results of the probe in human tumor tissues are highly consistent with pathological staining results, highlighting its potential as an adjunct to surgical resection. In addition, intraoperative pathology section detection by fluorescent probe technology took half the time required for H&E staining. This research is poised to advance the application of fluorescent probes in tumor diagnosis and surgical excision assistance.

Abatement of algal extracellular organic matter by vacuum ultraviolet: Effect of dissolved oxygen and role of in-situ formed reactive oxygen species

Algal extracellular organic matter (EOM) in water produced during the outbreak of algal blooms is difficult to be effectively removed by conventional water treatment processes. Compared with ultraviolet (UV), vacuum ultraviolet (VUV) can additionally radiate 185 nm photons, and VUV can split water to produce reactive oxygen species (ROS) in-situ. Herein, abatement and characteristic variation of EOM under VUV irradiation and the mechanism were investigated. Results indicated that EOM abatement by VUV irradiation were significantly higher than that by UV irradiation. The mineralization rate constant of EOM under VUV was 2.25 times of that under UV. Besides, under VUV irradiation, the abatement efficiency of EOM was promoted with the increased dissolved oxygen (DO), and EOM with a lower initial concentration had a higher abatement efficiency. Intensities of characteristic fluorescence peaks of EOM decreased obviously after VUV irradiation, and removal rates of specific fluorescent organic components were ≥ 74.4%. Under VUV irradiation, organic matter in EOM with higher molecular weight was transformed into that with lower molecular weight. Moreover, hydroxyl radical (•OH) generated in-situ by VUV dissociating water with different DO was directly identified by fluorescence molecular probe technology, and the higher DO caused the higher production of •OH. Furthermore, the mechanism of EOM abatement by VUV was proposed. DO and the produced ROS enhanced the abatement efficiency of EOM, and they played important roles in EOM abatement. This study disclosed abatement characteristics of EOM under VUV irradiation and provided great value for expanding the utilization of VUV in water treatment.

Selective aggregation of hematite from quartz using charged polyacrylamides: In-situ sizing

Recovering fine valuable material has been a significant challenge in minerals processing. This primarily stems from insufficient collision opportunities between fine particles and bubbles, specifically when utilising traditional recovery methods such as froth flotation. This research endeavours to address this challenge by exploring the use of various commercially available, high molecular weight polymers- specifically polyacrylamide (PAM)- to selectively aggregate hematite from quartz. Investigation of the conditions in which selective aggregation of hematite over quartz occurs, with the goal to achieve aggregate sizes of between 20 and 150 μm, were undertaken. Targeting this size range ensure that conditions are optimised for future use in conventional mechanical flotation cells as an efficient mineral recovery method. The study investigates the selectivity of charged PAM towards hematite and quartz at pH 10, using adsorption studies. Anionic PAM demonstrates a preference for hematite, with a range of charge density studies, highlighting stronger adsorption capacity with lower charge density polymers. Using BlazeMetrics probe technology for in-situ sizing and imaging, it was observed that conditioning 50–300 g APAM per t of hematite resulted in aggregates in the range of 30–230 μm after 5 min. Interestingly, the charge density of APAM does not markedly affect the size of the hematite aggregates, although altering the charge density of the polymer impacts the selectivity towards quartz. Additionally, cationic PAM results in the simultaneous aggregation of both hematite and quartz, not demonstrating selectivity. To mitigate heterocoagulation between minerals, a common dispersant, sodium hexametaphosphate (SHMP), was employed, which notably prevents quartz aggregation. Separation of aggregated hematite from quartz by sedimentation was only slightly effective with the majority of quartz settling with the hematite. Adding up to 1000 g of dispersant per t of hematite reduced the amount of quartz in the sediment bed by 23 %. The dispersant increased the magnitude of the negative zeta potential of the two minerals, particularly hematite, lowering heterocoagulation and improving effectiveness of hematite flocculation.

Generic Reporter Sets for Colorimetric Multiplex dPCR Demonstrated with 6-Plex SNP Quantification Panels.

Digital PCR (dPCR) is a powerful method for highly sensitive and precise quantification of nucleic acids. However, designing and optimizing new multiplex dPCR assays using target sequence specific probes remains cumbersome, since fluorescent signals must be optimized for every new target panel. As a solution, we established a generic fluorogenic 6-plex reporter set, based on mediator probe technology, that decouples target detection from signal generation. This generic reporter set is compatible with different target panels and thus provides already optimized fluorescence signals from the start of new assay development. Generic reporters showed high population separability in a colorimetric 6-plex mediator probe dPCR, due to their tailored fluorophore and quencher selection. These reporters were further tested using different KRAS, NRAS and BRAF single-nucleotide polymorphisms (SNP), which are frequent point mutation targets in liquid biopsy. We specifically quantified SNP targets in our multiplex approach down to 0.4 copies per microliter (cp/µL) reaction mix, equaling 10 copies per reaction, on a wild-type background of 400 cp/µL for each, equaling 0.1% variant allele frequencies. We also demonstrated the design of an alternative generic reporter set from scratch in order to give detailed step-by-step guidance on how to systematically establish and optimize novel generic reporter sets. Those generic reporter sets can be customized for various digital PCR platforms or target panels with different degrees of multiplexing.

Aberration correction in 3D transthoracic echocardiography

Three-dimensional cardiac imaging has been available in the clinic for more than two decades. Continuous improvement in image quality has occurred in this period due to the development of probe technology and beamforming techniques. The purpose of this article is to quantitatively and qualitatively analyze the effect of a commercially available aberration correction algorithm on clinically acquired 3D transthoracic echocardiography (3D TTE) images. Clinical triplane and 3D volume cineloops of at least one cardiac cycle of pre-beamformed channel data were captured from 50 patients using a GE HealthCare Vivid E95 system with the 4Vc-D matrix array probe. This resulted in a total of 3200 vol and 3136 triplane frames. The data were post-processed with and without aberration correction. Quantitatively, assessed by an image quality parameter based on coherence, all recordings were improved by aberration correction compared to those without aberration correction. Triplane data obtained a larger improvement in image quality than volume data. Qualitatively, as demonstrated by case examples, aberration-corrected images appear sharper, have a brighter tissue signal compared to the cavity, and provide better delineation of cardiac structures. 3D rendering of valves can also be significantly improved. In general, aberration correction provides a systematic improvement in clinical cardiac triplane and 3D volume images.

A DNA-peptide probe coupled mass spectrometry-based method for the detection of LncRNA in hepatocyte and serum samples

Liver cancer, a prominent contributor to cancer-related deaths, necessitates timely identification for successful intervention. In recent years, long non-coding RNAs (lncRNAs) have gained attention as potential biomarkers for liver cancer, and accurate quantification of lncRNA is essential for early diagnosis of liver cancer. However, existing methods for lncRNA detection rely on amplification and labeling techniques, resulting in semi-quantitative or qualitative outcomes. DNA-peptide technology offers a promising alternative. It has successfully translated nucleic acid quantification into peptide quantification, particularly in the context of miRNA analysis. However, the intricate structure of long-chain lncRNAs presents a challenge not encountered with miRNAs, making the design and acquisition of specific DNA-peptide probes for direct quantification more difficult. In this study, a strategy for lncRNA quantification was developed using a DNA-peptide probe coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based quasi-targeted proteomics. The inherent structural complexity of long-chain lncRNAs was overcome by designing DNA-peptide probes based on their unique sequence segments, enabling direct quantification without the need for amplification. Highly upregulated in liver cancer (HULC) was identified as a target lncRNA through bioinformatics analysis using GEO2R online software. Subsequently, the target lncRNA (i.e., HULC), which had been biotinylated and bound to streptavidin agarose beforehand, was hybridized with the probe. Following trypsin digestion, the reporter peptide was released and quantified using LC-MS/MS. Finally, this method was applied to analyze HULC levels in liver cancer cell lines and serum samples, enabling quantitative assessment and early diagnosis. The results demonstrated that liver cancer diagnostics could be enhanced through the integration of mass spectrometry and DNA-peptide probe technology for lncRNA quantification.

Enzyme-Programmed Self-Assembly of Nanoparticles.

Nanoparticles are a hot topic in the field of nanomaterial research due to their excellent physical and chemical properties. In recent years, DNA-directed nanoparticle self-assembly technology has been widely applied to the development of numerous complex nanoparticle superstructures. Due to the inherent stability and surface electric repulsion of nanoparticles, it is difficult to make nanoparticle superstructures respond to molecular signals in the external environment. In fact, enzyme-programmed molecular systems are developed to allow diverse functions, including logical operations, signal amplification, and dynamic assembly control. Therefore, combining enzyme-controlled DNA systems may endow nanoparticle assembly systems with more flexibility in program design, allowing them to respond to a variety of external signals. In this review, we summarize the basic principles of enzyme-controlled DNA/nanoparticle self-assembly and introduce its applications in heavy metal detection, gene expression, proteins inside living cells, cancer cell therapy, and drug delivery. With the continuous development of new nanoparticle materials and the increasing functionality of enzyme DNA circuits, enzyme-directed DNA/nanoparticle self-assembled probe technology is expected to see significant future development.

Synthesis and characterization of Co(II) porphyrin complex supported on chitosan/graphene oxide nanocomposite for efficient green oxidation and removal of Acid Orange 7 dye

Catalytic degradation of Acid Orange 7 (AO7) by hydrogen peroxide in an aqueous solution has been investigated using cobalt(II) complex of 5, 10, 15, 20 Tetrakis [4-(hydroxy)phenyl] porphyrin [Co(II) TPHPP] covalently supported chitosan/Graphene Oxide nanocomposite [Co(II) TPHPP]-Cs/GO, as highly efficient and recoverable heterogeneous catalyst. The structures and properties of [Co(II) TPHPP]-Cs/GO nanocomposite were characterized by techniques such as UV–Vis, FT-IR, SEM, EDX, TEM, and XRD. The oxidation reaction was followed by recording the UV–Vis spectra of the reaction mixture with time at λmax = 485 nm. [Co(II) TPHPP]-Cs/GO nanocomposite demonstrated high catalytic activity and could decompose 94% of AO7 within 60 min. The factors that may influence the oxidation of Acid Orange 7, such as the effect of reaction temperature, pH, concentration of catalyst, Acid Orange 7, and hydrogen peroxide, have been studied. The results of total organic carbon analysis (TOC) showed 50% of dye mineralization under mild reaction conditions of AO7 (1.42 × 10−4M) with H2O2 (8 × 10−2M) in the presence of [Co(II) TPHPP]-Cs/GO nanocomposite (15 × 10−3 g/ml) and pH = 9 at 40 °C. The reuse and stability of the nanocomposite were examined and remarkably, even after six cycles of reuse, there was no significant degradation or deactivation of the recycled catalyst. Residual organic compounds in the reaction mixture were identified by using GC–MS analyses. The radical scavenging measurements and photoluminescence probing technology of disodium salt of terephthalic acid indicated the formation of the hydroxyl radical as the reactive oxygen species in the [Co(II) TPHPP]-Cs/GO nanocomposite/H2O2 system. A mechanism for the oxidation reaction has been discussed.

Esophageal impedance planimetry during per-oral endoscopic myotomy guides myotomy extent

IntroductionPeroral endoscopic myotomy (POEM) is the standard treatment for achalasia. Functional luminal imaging probe (FLIP) technology enables objective measurement of lower esophageal sphincter (LES) geometry, with literature linking specific values to improved post-POEM outcomes. Our study assesses FLIP’s intraoperative use in evaluating myotomy extent in real-time.MethodsRetrospective data from all patients undergoing POEM with intraoperative FLIP measurements were extracted from June 2020 to January 2023. The primary endpoint was intraoperative FLIP measurements, management changes, and symptom improvement (Eckardt score).ResultsFourteen patients (age 56 ± 14 years, BMI 28 ± 7 kg/m2) were identified. Most patients were female (64%). Predominantly, patients presented with type II achalasia (50%). FLIP measurements were taken before and after myotomy, demonstrating increases in mean distensibility index (DI) 1.6 ± 1. 4 to 5.4 ± 2.1 mm2/mmHg (p < 0.05) and mean diameter (Dmin) 6 ± 1.8 to 10.9 ± 2.3 mm (p < 0.05) at 50 ml balloon fill. Additional myotomy was performed in one patient when an inadequate increase in FLIP values were noted. Mean operative time was 98 ± 28 min, and there were no intraoperative complications. At the 30-day follow-up, median Eckardt score decreased from mean a preoperative score of 7 ± 2 to a post-operative mean of 2 ± 3, with 10 patients (78%) having a score ≤ 2. In total, four patients experienced symptom recurrence, with repeat FLIP values revealing a significant decrease in DI from 7 ± 2.2 post-POEM to 2.5 ± 1.5 at recurrence. FLIP technology identified LES pathology in 3 out of 4 (75%) patients, facilitating referral to LES-directed therapy.ConclusionOur study adds to the literature supporting the use of FLIP technology during the POEM procedure, with most patients achieving ideal values after a standard-length myotomy. This suggests the potential benefits of shorter myotomies guided by FLIP to achieve comparable outcomes and reduce postoperative GERD risk. Collaborative standardization of study designs and outcome measures is crucial for facilitating prospective trials and cross-setting outcome comparisons.Graphical abstract

Nonlinear optical absorption and ultrafast carrier dynamics in layered tin diselenide quantum dots

Quantum dots (QDs) derived from typical two-dimensional materials present attractive unique chemical and physical properties because of the quantum-confinement effect. Herein, high-quality layered tin diselenide (SnSe2) QDs with controllable size and thickness were prepared from layered bulk SnSe2 crystals using a simple, effective, and economical mechanical and liquid exfoliation technique. The resulting SnSe2 QDs were subsequently incorporated into chemically stable transparent silica-gel glasses using a sol–gel method. The nonlinear optical (NLO) absorption of the SnSe2 QDs was systematically explored using a combination of open-aperture Z-scan and pump–probe technologies. The derived NLO parameters and ultrafast carrier dynamics of the QDs were comparable to those of reported low-dimensional materials. Interestingly, the layered SnSe2 QDs exhibited thickness/layer-dependent NLO properties and pulse duration-dependent saturable absorption and reverse saturable absorption in both dimethylformamide suspensions and solid silica-gel glasses. Such unique NLO characteristics make layered SnSe2 QDs a promising candidate for technological innovations in areas including optoelectronics and nonlinear optics.

A primitive cell model involving Vesicles, microtubules and asters

HypothesisSimple single-chain amphiphiles (sodium monododecyl phosphate, SDP) and organic small molecules (isopentenol, IPN), both of primitive relevance, are proved to have been the building blocks of protocells on the early Earth. How do SDP-based membrane and coexisting IPN come together in specific ways to produce more complex chemical entities? What kind of cell-like behavior can be endowed with this protocell model? These are important questions in the pre-life chemical origin scenario that have not been answered to date. ExperimentsThe phase behavior and formation mechanism of the aggregates for SDP/IPN/H2O ternary system were characterized and studied by different electron microscopy, fluorescent probe technology, DLS, IR, ESI-MS, SAXS, etc. The stability (freeze–thaw and wet-dry treatments) and cell-like behavior (chemical signaling communication) were tested via simulating particular scenarios. FindingsVesicles, microtubules and asters phases resembling the morphology and structure of modern cells/organelles were obtained. The intermolecular hydrogen bonding is the main driving force for the emergence of the aggregates. The protocell models not only display remarkable stabilities by simulating the primordial Earth’s diurnal temperature differences and ocean tides but also are able to exhibit cell-like behavior of chemical signaling transition.

Inflammatory Gene Panel Guiding the Study of Genetics in Inflammatory Bowel Disease.

Inflammatory bowel disease (IBD) is a complex disease that develops through a sequence of molecular events that are still poorly defined. This process is driven by a multitude of context-dependent genes that play different roles based on their environment. The complexity and multi-faceted nature of these genes make it difficult to study the genetic basis of IBD. The goal of this article is to review the key genes in the pathophysiology of IBD and highlight new technology that can be used in further research. This paper examines Nanostring RNA probe technology, which uses tissue analyzed without the use of enzymes, transcription, or amplification. Nanostring offers several panels of genes to test, including an inflammation panel of 234 genes. This article analyzes this panel and reviews the literature for each gene's effect in IBD for use as a framework to review the pathophysiology of the disease. The panel was narrowed to 26 genes with significant evidence of mechanistic potential in IBD, which were then categorized into specific areas of pathogenesis. These include gut barrier breakdown, inappropriate recognition of commensal bacteria, immune cell activation, proinflammatory cytokine release, and subsequent impairment of the anti-inflammatory response. The eventual goal of this paper is the creation of a customized panel of IBD genes that can be used to better understand the genetic mechanism of IBD and aid in the development of future therapies in IBD.