NEOPLASIA
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2021
·
IF 5.715
Yihui Ma,Peiyi Xia,Zhengyang Wang,Jingjing Xu,Lan Zhang,Yanan Jiang
Protein Disulfide Isomerase Family A Member 6 (PDIA6) is an endoplasmic reticulum protein that is capable of catalyzing protein folding and disulfide bond formation. Abnormally elevated expression of PDIA6 has been reported to predict poor outcomes in various cancers. Herein, gain-of- and loss-of-function experiments were performed to investigate how PDIA6 participated in the carcinogenesis of pancreatic cancer (PC). By analyzing the protein expression of PDIA6 in 28 paired PC and para carcinoma specimens, we first found that PDIA6 expression was higher in PC samples. Both the overall survival and disease-free survival rates of PC patients with higher PDIA6 expression were poorer than those with lower PDIA6 ( n = 178). Furthermore, knockdown of PDIA6 impaired the malignancies of PC cells — suppressed cell proliferation, invasion, migration, cisplatin resistance, and xenografted tumor growth. PDIA6-silenced PC cells were more sensitive to cytotoxic natural killer (NK) cells. Overexpression of PDIA6 had opposite effects on PC cells. Interestingly, COP9 signalosome subunit 5 (CSN5), a regulator of E3 ubiquitin ligases known to promote deubiquitination of its downstream targets, was demonstrated to interact with PDIA6, and its expression was increased in PC cells overexpressing PDIA6. Additionally, PDIA6 overexpression promoted deubiquitination of β-catenin and PD-L1 and subsequently upregulated their expression in PC cells. These alterations were partly reversed by CSN5 shRNA. Collectively, the above results demonstrate that PDIA6 contributes to PC progression, which may be associated with CSN5-regulated deubiquitination of β-catenin and PD-L1. Our findings suggest PDIA6 as a potential target for the treatment of PC.
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REACTIVE & FUNCTIONAL POLYMERS
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2021
·
IF 3.975
Yue Zhang,Lizhen Yu,Jun Zhu,Renmin Gong
In this paper, a novel grafted polymer (folate and carboxymethyl-β-cyclodextrin grafted trimethyl chitosan, FCT) was synthesized. Then the FCT nanoparticles (FCT NPs) were fabricated by ionic gelation and the potential of NPs as co-carrier of doxorubicin and siRNA was evaluated. The physicochemical properties of grafted polymer and NPs were characterized and analyzed by fourier transforms infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential and polydispersity index (PDI). The results showed the diameter of NPs ranged from 190 to 240 nm with polydispersity index of 0.192 and zeta potential of +21mv. The prepared NPs exhibited satisfactory drug loading capacity and encapsulation efficiency to doxorubicin and siRNA-survivin. Meanwhile, the prepared NPs could effectively protect siRNA-survivin from degradation of serum RNAase for a long time. Both drugs encapsulated in NPs all exhibited pH-dependent controlled sustained release characteristics and the cytotoxicity study testified that drug drug-loaded FCT NPs significantly improved the efficacy of antitumor drugs . The novel graft polymer was expected to become the co-carrier of anticancer and gene drugs in future with broad application prospects.
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ACS Applied Materials & Interfaces
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2021
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IF 9.229
Jun Zhang,Tiantian Zuo,Jie Yang,Zongwei Hu,Zhihua Wang,Rui Xu,Siyu Ma,Yawen Wei,Qi Shen
The aggressive progression of breast cancer is impacted significantly by the tumor microenvironment (TME). The current chemotherapy normally causes cytotoxicity to tumor cells, while does not effectively modulate the TME. Thus, the chemotherapy effect of breast cancer is usually dissatisfactory. In this study, a kind of hierarchically releasing bio-responsive nanoparticles (R(D)/H(S) NPs), constructed by β-cyclodextrin-grafted heparin and pH-sensitive pseudorotaxane, were investigated to enhance the breast cancer chemotherapeutic efficacy through TME modulation. Doxorubicin (DOX) and transforming growth factor-β (TGF-β) receptor inhibitor (SB431542) loaded onto R(D)/H(S) NPs were released rapidly for the respective response to low pH in endosomes/lysosomes and heparanase (HPSE) in TME. Our results showed that R(D)/H(S) NPs effectively inhibited the formation of tumor-associated fibroblasts (TAFs) and reduced TGF-β and collagen I secretion. Besides, the immunosuppressive microenvironment was effectively reversed into immunogenic, characterized by increased CD8+ and CD4+ T cell infiltration, which distinctly inhibited breast cancer metastasis. Therefore, R(D)/H(S) NPs remodeled the TME by downregulating TAFs, TGF-β, and collagen I; activating the immune microenvironment; and then amplifying the chemotherapeutic efficacy of DOX.
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ANALYTICAL CHEMISTRY
·
2020
·
IF 6.785
Yu Wang,Yu Xue,Shuang Wang,Jianshe Huang,Xiurong Yang
One of the pathogenesis hypotheses of Alzheimer’s disease (AD) is amyloid depositions and neurofibrillary tangles. Apolipoprotein E (Apo E) acts a vital part in the development of AD by affecting the aggregation and clearance of amyloid-β (Aβ). In this paper, a dual polarization interferometry (DPI) technique was employed for a real-time investigation toward the binding events of Apo E isoforms, for instance, Apo E2, Apo E3, and Apo E4, with Aβ1–40. By evaluation of detailed binding information provided by DPI, the affinities between Apo E isoforms and Aβ1–40 follow the order of E4 > E3 > E2, and the dissociation constants (KD) of Aβ1–40 with Apo E2, Apo E3, and Apo E4 were determined to be 251 ± 37, 40 ± 0.65, and 24.6 ± 2.42 nM, respectively. Our findings reveal the isoform-specific binding behaviors from a kinetics perspective, which can help us understand that Apo E4 has a higher risk of causing AD because of its promoting effect on Aβ aggregation and fibrillation and inefficient clearance of Aβ. Remarkably, this work provides a promising method for exploring the dynamics of interactions between biomolecules and expectantly contributes to the development of AD drugs and therapies targeting Apo E and Aβ.
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ENZYME AND MICROBIAL TECHNOLOGY
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2020
·
IF 3.448
Ting Liu,Baoyou Pei,Jinqing Lin,Guangya Zhang
β-1,3-xylanase plays an important role in the conversion of algal biomass into renewable chemical commodities and functional xylooligosaccharides. Efficient immobilization of the target enzymes that could integrate the separation, purification, and immobilization in one-step may have great potentials. The cheap and easily obtained pitch was adopted as the raw material to prepare the hyper-cross-linked polymers with the specific surface areas of 560 m 2 /g and the Ni 2+ loading about 80 mg/g. As a carrier, it could immobilize and purify the β-1,3-xylanases directly from the crude cell debris with the activity recovery of (80.66 ± 0.87) %. The half-life of the immobilized β-1,3-xylanases was 50 min at 50 °C, which was significantly longer than the free ones with only 14 min. The immobilized β-1,3-xylanases could retain 65 % of the activity after stored at 30 ℃ for 80 h, they could also retain 87 % of the original activity after 15 cycles of reuse. In terms of potential applications in the manipulation of algae Caulerpa lentillifera , the immobilized β-1,3-xylanases could release 30 % more reducing sugar in 85 h. The method proposed here is promising for algal biomass manipulation because of its low cost, stable storage, convenient recycling and excellent reusability.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2020
·
IF 7.489
Dongli Li,Kungang Chai,Xingdong Yao,Liqin Zhou,Kongyou Wu,Zhenghui Huang,Juntao Yan,Xingzhen Qin,Wei Wei,Hongbing Ji
To remove the bulky aqueous organic dye e.g. methyl blue (MB) from water, ordered mesoporous silica SBA-15 has been functionalized with β-cyclodextrin (β-CD) via amide linkage. The surface physical and chemical properties of the surface of the resulted β-CD-functionalized adsorbents (abbrev. SBA15-A-CD) were characterized systematically. The results indicate that the channels of SBA-15 were uniformly modified with amine groups and were further β-CD-terminated via amide linkages, without ruining its ordered mesoporous structure. The effects of contact time, pH, ionic strength, temperature and salt on the adsorption performance were explored. SBA15-A-CD showed maximum adsorption capacity for MB up to 1791 mg·g −1 combined with excellent recyclability. Besides, the adsorption behavior of MB onto SBA15-A-CD has been investigated by DFT calculation and two-dimensional NMR. Specifically, the enhanced adsorption capacity for MB stems from the tailored host–guest interaction between β-CD cavity and aromatic moiety of MB in combination with the electrostatic attraction between amine groups and sulfonated group of MB. These findings offer good opportunities for improving the ability of mesoporous silica in adsorption of bulky anion dyes in wastewater.
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CARBOHYDRATE POLYMERS
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2020
·
IF 7.182
Siyi Li,Na Liang,Pengfei Yan,Yoshiaki Kawashima,Shaoping Sun
Insulin is the most effective drug in the treatment of diabetes mellitus. At present, subcutaneous injection is still the common way for insulin delivery. However, oral delivery is considered as the most preferred way for its high patient compliance and the minimal invasiveness. In this study, a novel N -acetyl- L -cysteine and arginine modified hydroxypropyl-β-cyclodextrin (NAC-HP-β-CD-Arg) was successfully synthesized and characterized. The polymer was used as a carrier for oral delivery of insulin by forming NAC-HP-β-CD-Arg@insulin complex. Enzymatic degradation study indicated that the NAC-HP-β-CD-Arg could protect insulin from enzymolysis. Moreover, the polymer exhibited strong binding ability with mucin. The transportation efficiency of NAC-HP-β-CD-Arg@insulin across the Caco-2 cell monolayer was much greater than free insulin. The in vivo study demonstrated that the orally administered NAC-HP-β-CD-Arg@insulin exhibited an excellent and sustained hypoglycemic effect in diabetic rats. It can be concluded that the NAC-HP-β-CD-Arg is a potential carrier for oral delivery of insulin.
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OPTICAL MATERIALS
·
2020
·
IF 2.779
Hua Li,Xiaobo Shi,Xia Li,Lingbo Zong
Size-tunable β-NaYF 4 : Yb/Er (50–400 nm) up-converting nanoparticles (UCNPs) with a strong green emission were successfully prepared by a facile thermal decomposition method in a short period of time. The effects of the reaction time, the oleic acid (OA) content, and the doped Gd 3+ concentration on the crystal structure, the size evolution mechanism and the luminescence mechanism of the β-NaYF 4 : Yb/Er nanoparticles were discussed in detail. Characterization was completed using X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution (HR-TEM), scanning electron microscopy (SEM), and photoluminescence (PL). The results reveal that the phase transition was completed at 15 min and the morphology of the NaYF 4 : Yb/Er UCNPs changed from spherical to large hexagonal disks (200–400 nm) in non-doped Gd 3+ . An appropriate decrease in the volume ratio of oleic acid (OA) to 1-octadecene (ODE) promoted NaF production, resulting in the formation of the hexagonal phase crystals and the subsequent increase of luminous intensity by 30–40 times. More importantly, the size of the β-NaYF 4 : Yb/Er decreased with Gd 3+ doping, and the UCNPs ultimately transformed into small hexagonal prisms (50 nm) with high monodispersity when the doping concentration of Gd 3+ was 60 mmoL. The PL spectra confirmed that the luminous intensity of the UCNPs with doped Gd 3+ was much higher than that of the undoped UCNPs. The results show that this route for UCNP fabrication with high luminous efficiency and a small size could be extended to other UCNP systems for multifunctional biomedical applications.
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BIOMACROMOLECULES
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2021
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IF 6.988
Shuai Zhu,Ruizhong Xue,Zikun Yu,Xu Zhang,Shifang Luan,Haoyu Tang
Poly(l-cysteine)s with methylthio pendants (PMTLCs) were synthesized by ring-opening polymerization of a new l-cysteine-based N-carboxyanhydride. The thioether bonds of PMTLC can be readily oxidized by H2O2 yielding water-soluble PMTLCOX. The methylthio groups can undergo an alkylation reaction using methyl iodide and a subsequent ion-exchange reaction yielding sulfonium-based polypeptides (PPLC-DMS-X, where X = I, BF4). PPLC-DMS-X showed upper critical solution temperature-type thermo- and oxidation-responsive properties in aqueous solutions. Both PMTLC and PPLC-DMS-X showed oxidation-induced β-sheet to α-helix transitions. The absorbance of PPLC-DMS-I and methyl orange aqueous solution displayed a significant linear correlation with temperature, which makes the sulfonium-based polypeptides good candidates in the field of temperature sensors.
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Catalysts
·
2020
·Vol. 10
·期 12
·1419
·
IF 3.52
Li-Hua Du,Miao Xue,Meng-Jie Yang,Yue Pan,Ling-Yan Zheng,Zhi-Min Ou,Xi-Ping Luo
An efficient method for the preparation of β-amino alcohols catalyzed by lipase TL IM fromThermomyces lanuginosusin a continuous-flow reactor was developed. The eco-friendly biocatalyst combined with continuous-flow reaction technology displayed high efficiency in the synthesis of β-amino alcohols. The benign reaction conditions (35 °C) and short residence time (20 min), together with the use of low cost and readily available starting materials, make this synthetic approach a promising alternative to current β-amino alcohol synthesis.Keywords:enzymatic synthesis;β-amino alcohols;reactor;epoxides;ring-opening reaction
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Journal of Materials Chemistry B
·
2020
·Vol. 8
·期 48
·10966-10976
·
IF 5.344
Han Fu,Junping Liu,Wu Xu,Haixiang Wang,Shenghua Liao,Guitang Chen
In this paper, a new magnetic molecular imprinted polymer–cyclodextrin (MMIP–CD) material was prepared by connecting β-cyclodextrin (CD) on the surface of a magnetic molecular imprinted polymer (MMIP) and used for the rapid and specific adsorption of zearalenone (ZEN). By using warfarin as the virtual template molecule, tetraethyl orthosilicate (TEOS) as the crosslinking agent, and (3-aminopropyl) triethoxysilane (APTES) as the functional monomer, a MMIP was produced by surface imprinting technology. Sulfobutyl ether-β-cyclodextrin attached to the surface of the MMIP under heating conditions produced a new specific adsorption material with exceptional adsorption capacity and excellent selectivity for ZEN. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and TEM-mapping results showed that the prepared MMIP–CD had a uniform particle size of about 480 nm, and the molecularly imprinted layer was successfully wrapped on the surface of the nanoparticles with a thickness of about 50 nm, whereby the cyclodextrin was effectively attached to the surface of the MMIP. The adsorption mechanism of MMIP–CD was confirmed by kinetic adsorption and thermodynamic adsorption experiments, the maximum adsorption capacity was found to be about 30 mg g−1, and the adsorption equilibrium could be reached within 20 min. The value of IF (QMMIP–CD/QMNIP) is 4.642. This showed that compared with MNIP, MMIP–CD showed a greatly improved specific adsorption capacity of ZEN. Selective experiments proved that MMIP–CD effectively combined the advantages of MMIP and CD, enhancing the adsorption capacity together with reducing the disadvantages that MMIP cannot distinguish structural analogs and CD cannot identify hydrophobic compounds effectively. In actual sample testing, the limit of quantification (LOQ) and limit of detection (LOD) were 0.1 ng kg−1 and 0.3 ng kg−1, respectively. The stability and detection precision of this method were 0.98–2.76% and 1.67–3.88%, respectively. The results proved that MMIP–CD had good development potential in the field of selective adsorption of ZEN, and laid the foundation for follow-up research.
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Environmental Science-Nano
·
2021
·Vol. 8
·期 3
·773-783
·
IF 8.131
Haixia Wang,Dong Liang,Yan Xu,Xiang Liang,Xiaoqing Qiu,Zhang Lin
The development of an effective and stable photochemical sensor is urgently needed to solve the growing environmental pollution problem caused by immoderate usage of the organic phosphorus pesticide, chlorpyrifos. Under the circumstances, 2D/2D Z-scheme β-Bi2O3/g-C3N4 heterojunctions have been attempted to fabricate a photoelectrochemical sensor, which can detect chlorpyrifos selectively and sensitively. The 2D/2D intimate contact interfaces could facilitate the separation and migration of electron–hole pairs. Consequently, β-Bi2O3/g-C3N4 composites possess higher photocurrent response than single β-Bi2O3 and g-C3N4. After incubation with chlorpyrifos, in situ formed Bi–chlorpyrifos complex blocks the transformation of photogenerated charges, and thus contributes to a dramatic decline in photocurrent signal intensity and selective determination of chlorpyrifos. The novel photoelectrochemical sensor with strong stability presents a perfect linear relationship between photocurrent intensity and logarithm of chlorpyrifos concentration ranging from 0.01 to 80 ng mL−1, and displays excellent properties over a wide linear range with an ideal detection limit of 0.03 ng mL−1 (S/N = 3). To some extent, the Z-scheme β-Bi2O3/g-C3N4 sensor is promising for the detection of chlorpyrifos pesticides in practical environmental pollution treatment applications.
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