Publications by authors named "X-F Cao"

Circulating tumor cells (CTCs) in the bloodstream are important biomarkers for clinical prognosis of cancers. Current CTC identification methods are based on immuno-labeling, which depends on the differential expression of specific antigens between the cancer cells and white blood cells. Here we present an antigen-independent CTC detection method utilizing a deep-learning-assisted single-cell biolaser.

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Engineering F-rich solid electrolyte interphase (SEI) layers is regarded as an effective strategy to enable the long-term cycling stability of potassium-ion batteries (KIBs). However, in the conventional KPF carbonate electrolytes, it is challenging to form F-containing SEI layers due to the inability of KPF to decompose into KF. Herein, AlCl is employed as a novel additive to change the chemical environment of the KPF carbonate electrolyte.

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Article Synopsis
  • The study investigates the geometric and electronic structures of acetonitrile-solvated dodecaborate clusters, revealing that electron binding energies increase with cluster size, indicating better electronic stability.
  • Each acetonitrile molecule forms strong dihydrogen bonds with the dodecaborate, with notable structural changes observed as more acetonitrile molecules are added.
  • The research uses advanced computational methods to validate experimental findings and highlights the significance of acetonitrile as a strong hydrogen bond donor in stabilizing these clusters.
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The harpoon mechanism has been a milestone in molecular reaction dynamics. Until now, the entity from which electron harpooning occurs has been either alkali metal atoms or non-metallic analogs in their excited states. In this work, we demonstrate that a common organic molecule, octamethylcalix[4] pyrrole (omC4P), behaves just like alkali metal atoms, enabling the formation of charge-separated ionic bonding complexes with halogens omC4P ⋅ X (X=F-I, SCN) via the harpoon mechanism.

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Negative ion photoelectron spectra at 20 K along with ab initio [CCSD(T)] and M06-2X density functional theory calculations are reported for a series of six basic and nucleophilic pyridine derivatives with an anionic substituent [i.e., 3- and 4-PyrBX, where X = F, 4--BuCH, 4-MeOCH, and 3,5-(MeO)CH].

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Background: Endothelial dysfunction plays a crucial role in aortic remodeling. Aerobic glycolysis and endothelial-to-mesenchymal transition (EndoMT) have, respectively, been suggested to contribute to endothelial dysfunction in many cardiovascular diseases. Here, we tested the hypothesis that glycolytic reprogramming is critical for EndoMT induction in aortic remodeling through an epigenetic mechanism mediated by a transcriptional corepressor CtBP1 (C-terminal binding protein 1), a sensor of glycolysis-derived NADH.

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Introduction: To investigate the efficacy and safety of preprocedural simethicone (S) and pronase (P) for optimal mucosal visualization during esophagogastroduodenoscopy with sedation. The effect of postural change combined with premedication on mucosal visibility was also examined.

Methods: The study randomized 496 patients into 8 groups based on the type of premedication provided and whether a postural change occurred.

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Very recently, bioinspired high-valence metal-halogen complexes have been proven to be competent oxidants in the C-H bond activation and heteroatom dihalogenation reactions. However, the structure-activity relationship of such active species and the reaction mechanisms of oxidations mediated by these oxidants are still elusive. In this study, density functional theory (DFT) calculations were performed to systematically study the oxidizing ability of the high-valence Ni-X (X = F and Cl) complexes EtN[Ni(Cl/F)(L)], (1, Et = ethyl, L = '-(2,6-dimethylphenyl)-2,6-pyridinedicarboxamide), such as the reaction mechanism of fluorination of 1,4-cyclohexadiene (CHD) by 1 in the presence of AgF and the reaction mechanism of difluorination of triphenyl phosphine (PPh) by 1.

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The geometric structure, energy properties, and electronic properties of the aerogen-bonding interaction formed by CH and NgOX (Ng = Kr, Xe; X = F, Cl, Br) have been studied at the B2PLYP-D3(BJ)/ aug-cc-pVTZ (PP) level. Two kinds of aerogen-bonding interactions were observed among the title systems: the σ-hole and the π-hole complexes. The σ-hole aerogen-bonding complex has a binding energy in the range of - 6.

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Article Synopsis
  • Hydridic-to-protonic dihydrogen bonds (DHBs) play a crucial role in influencing the structure and reactivity of chemical systems, with significant challenges in understanding their strength and bonding nature.
  • This study utilized photoelectron spectroscopy and theoretical modeling to investigate monohydrated dodecaborate clusters, revealing that B-H⋯H-O DHBs are significantly stronger than traditional hydrogen bonds involving other elements (B-X⋯H-O).
  • The research highlights the importance of DHBs in aqueous environments and suggests that optimizing these interactions could lead to more efficient and environmentally friendly methods for catalytic dihydrogen production.
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The highly pathogenic and readily transmissible SARS-CoV-2 has caused a global coronavirus pandemic, urgently requiring effective countermeasures against its rapid expansion. All available vaccine platforms are being used to generate safe and effective COVID-19 vaccines. Here, we generated a live-attenuated candidate vaccine strain by serial passaging of a SARS-CoV-2 clinical isolate in Vero cells.

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It is a challenge to effectively reactivate preexisting tumor-infiltrating lymphocytes (TILs) without causing severe toxicity. Interleukin-12 (IL-12) can potently activate lymphocytes, but its clinical use is limited by its short half-life and dose-related toxicity. In this study, we developed a tumor-conditional IL-12 (pro-IL-12), which masked IL-12 with selective extracellular receptor–binding domains of the IL-12 receptor while preferentially and persistently activating TILs after being unmasked by matrix metalloproteinases expressed by tumors.

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The 24 trioxide halide molecules MOX of the manganese group (M = Mn-Bh; X = F-Ts), which are iso-valence-electronic with the famous MnO ion, have been quantum-chemically investigated by quasi-relativistic density-functional and ab initio correlated approaches. Geometric and electronic structures, valence and oxidation numbers, vibrational and electronic spectral properties, energetic stabilities of the monomers in the gas phase, and the decay mode of MnOF have been investigated. The light Mn-3d species are most strongly electron-correlated, indicating that the concept of a closed-shell Lewis-type single-configurational structure [Mn(d) O(p) F(p)] reaches its limits.

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Background And Purpose: Hemorrhage-caused gene changes in the thalamus likely contribute to thalamic pain genesis. RNA N6-methyladenosine modification is an additional layer of gene regulation. Whether FTO (fat-mass and obesity-associated protein), an N6-methyladenosine demethylase, participates in hemorrhage-induced thalamic pain is unknown.

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A fundamental understanding of cyclodextrin-closo-dodecaborate inclusion complexes is of great interest in supramolecular chemistry. Herein, we report a systematic investigation on the electronic structures and intramolecular interactions of perhalogenated closo-dodecaborate dianions B12X122- (X = F, Cl, Br and I) binding to α-, β-, and γ-cyclodextrins (CDs) in the gas phase using combined negative ion photoelectron spectroscopy (NIPES) and density functional theory (DFT) calculations. The vertical detachment energy (VDE) of each complex and electronic stabilization of each dianion due to the CD binding (ΔVDE, relative to the corresponding isolated B12X122-) are determined from the experiments along α-, β- and γ-CD in the form of VDE (ΔVDE): 4.

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Background Microwave ablation (MWA) and radiofrequency ablation (RFA) have recently attracted interest as minimally invasive treatment modalities for papillary thyroid carcinoma (PTC). However, the ablation outcomes of T1N0M0 PTC are not well characterized. Purpose To evaluate the efficacy and safety of thermal ablation (MWA or RFA) of solitary T1N0M0 PTC in patients who were ineligible for (due to presence of comorbid cardiovascular disease, renal failure, other malignancy, etc) or who refused surgery.

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Li-rich cathode materials possess a much higher theoretical energy density than all intercalated cathode materials currently reported and thus are considered as the most promising candidate for next-generation high-energy density Li-ion batteries. However, the rapid voltage decay and the irreversible phase transition of O3-type Li-rich cathode materials often lessen their actual energy density and limit their practical applications, and thus, effectively suppressing the voltage decay of Li-rich cathodes becomes the hotspot of the current research. Herein, the F-doped O2-type Li-rich cathode materials LiMnNiCoOF (F-O2-LRO) are designed and prepared based on the P2-type sodium-ion cathode materials NaLi(MnNiCo)O (Na-LRO) by ion exchange.

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Acute kidney injury (AKI) causes multiple organ dysfunction. Here, we identify a possible mechanism that can drive brain vessel injury after AKI. We induced 30-minute bilateral renal ischemia-reperfusion injury in C57Bl/6 mice and isolated brain microvessels and macrovessels 24 hours or 1 week later to test their responses to vasoconstrictors and found that after AKI brain vessels were sensitized to Ang II (angiotensin II).

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Perfluorooctanoic acid (PFOA) is highly stable due to the strong CF bond and extremely difficult to be removed by conventional photocatalysts. In this study, Bi doped BiOIF solid solutions with hollow microsphere structure were prepared through a facile one-step hydrothermal method. Compared with pure BiOI and BiOF, the band gap of the Bi/BiOIF solid solutions was significantly reduced, thus promoting the visible light absorbance.

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This work shows elusive carbonic acid being effectively stabilized in the gas phase by interacting with halide anions X (X = F, Cl, Br, and I). The formed HCO·X complexes, characterized by negative ion photoelectron spectroscopy and ab initio calculations, all contain intact trans-trans carbonic acid binding onto the respective halide via two identical strong ionic O-HX hydrogen bonds. For X = Cl, Br, and I, the complex spectra exhibit the corresponding X signature by simply shifting to the higher binding energy side, while an extremely 2 eV wide broader band is observed for X = F.

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Introduction: Acute lung injury (ALI) is a fatal but undertreated condition with severe neutrophilic inflammation, although little is known about the functions of eosinophils in the pathogenesis of ALI. Our objectives were to investigate the roles and molecular mechanisms of eosinophils in ALI.

Methods: Pulmonary eosinophils were identified by flow cytometry.

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Background Coronavirus disease 2019 (COVID-19) has widely spread all over the world since the beginning of 2020. It is desirable to develop automatic and accurate detection of COVID-19 using chest CT. Purpose To develop a fully automatic framework to detect COVID-19 using chest CT and evaluate its performance.

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The interactions between hexafluoroisopropanol (HFIP) and halogen anions X (F, Cl, Br, and I) have been investigated using negative ion photoelectron (NIPE) spectroscopy and ab initio calculations. The measured NIPE spectrum of each [HFIP·X] (X = Cl, Br, and I) complex shows a pattern identical to the corresponding X by shifting to the high electron binding energy side, indicative of the formation of the [HFIP···X] structure in which X interacts with HFIP via charge-dipole interactions. However, the spectrum of [HFIP·F] appears completely different from that of F and is more similar to the spectrum of the deprotonated HFIP anion (HFIP).

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Background and Purpose- Previous results on the association between lipids and stroke were controversial. We investigated the association of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C ), high-density lipoprotein cholesterol (HDL-C), and triglyceride with stroke. Methods- Six cohort studies in China with 267 500 participants were included.

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