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991.
Nayden G. Naydenov Supriya Joshi Alex Feygin Siddharth Saini Larisa Litovchick 《Cell cycle (Georgetown, Tex.)》2018,17(14):1812-1831
Vesicle trafficking regulates epithelial cell migration by remodeling matrix adhesions and delivering signaling molecules to the migrating leading edge. Membrane fusion, which is driven by soluble N-ethylmaleimide-sensitive factor associated receptor (SNARE) proteins, is an essential step of vesicle trafficking. Mammalian SNAREs represent a large group of proteins, but few have been implicated in the regulation of cell migration. Ykt6 is a unique SNARE existing in equilibrium between active membrane-bound and inactive cytoplasmic pools, and mediating vesicle trafficking between different intracellular compartments. The biological functions of this protein remain poorly understood. In the present study, we found that Ykt6 acts as a negative regulator of migration and invasion of human prostate epithelial cells. Furthermore, Ykt6 regulates the integrity of epithelial adherens and tight junctions. The observed anti-migratory activity of Ykt6 is mediated by a unique mechanism involving the expressional upregulation of microRNA 145, which selectively decreases the cellular level of Junctional Adhesion Molecule (JAM) A. This decreased JAM-A expression limits the activity of Rap1 and Rac1 small GTPases, thereby attenuating cell spreading and motility. The described novel functions of Ykt6 could be essential for the regulation of epithelial barriers, epithelial repair, and metastatic dissemination of cancer cells. 相似文献
992.
993.
Chalada Suebsuwong Daniel M. Pinkas Soumya S. Ray Joshua C. Bufton Bing Dai Alex N. Bullock Alexei Degterev Gregory D. Cuny 《Bioorganic & medicinal chemistry letters》2018,28(4):577-583
Development of selective kinase inhibitors remains a challenge due to considerable amino acid sequence similarity among family members particularly in the ATP binding site. Targeting the activation loop might offer improved inhibitor selectivity since this region of kinases is less conserved. However, the strategy presents difficulties due to activation loop flexibility. Herein, we report the design of receptor-interacting protein kinase 2 (RIPK2) inhibitors based on pan-kinase inhibitor regorafenib that aim to engage basic activation loop residues Lys169 or Arg171. We report development of CSR35 that displayed >10-fold selective inhibition of RIPK2 versus VEGFR2, the target of regorafenib. A co-crystal structure of CSR35 with RIPK2 revealed a resolved activation loop with an ionic interaction between the carboxylic acid installed in the inhibitor and the side-chain of Lys169. Our data provides principle feasibility of developing activation loop targeting type II inhibitors as a complementary strategy for achieving improved selectivity. 相似文献
994.
Jessica St-Pierre Philippe J. Dufresne Alex Carignan Émilie Lévesque Francis Bernard Jean Longtin Louiselle LeBlanc 《Mycopathologia》2018,183(2):399-406
We report the two first cases of human C. gattii meningoencephalitis acquired on the Canadian east coast, from the province of Quebec. Unlike C. neoformans, C. gattii is not known to have an established ecological niche on the North American east coast. C. gattii has recently been responsible for major outbreaks in British Columbia, Canada, and in the American pacific northwest. However, no human cases acquired in other Canadian provinces have been reported to our knowledge. The source of acquisition remains unclear for both patients but since neither had traveled outside of the province of Quebec, we discuss the possibilities of environmental and animal-associated acquisition, as well as the possible established endemicity in new areas. These cases add to the growing reported human and animal cases in areas previously not thought to be endemic for C. gattii. 相似文献
995.
Monica Pinardi Elisa Soana Alex Laini Mariano Bresciani Marco Bartoli 《Biogeochemistry》2018,140(2):175-197
Ongoing socio-economic and climatic changes can differentially affect the biogeochemistry of the key nutrients nitrogen (N), silica (Si), and phosphorus (P) by altering their soil budgets, their transfer to aquatic environments and their ecological stoichiometry. This may lead to cascade consequences for aquatic communities and biogeochemical processes. Soil budgets, river export, and N, Si, and P ecological stoichiometry were assessed in a heavy impacted basin (Mincio River, Italy) in two decades (1991–2000; 2001–2010). The main aim was to analyse element-specific mechanisms of terrestrial-aquatic transport and retention within aquatic habitats. Budget results suggest a net accumulation (inputs exceeding outputs) of all nutrients in agricultural lands, mainly due to livestock manure, with a reduction for N (196 kg N ha?1 year?1 in 2000, and 132 kg N ha?1 year?1 in 2010), and constant values for Si (up to 3 kg Si ha?1 year?1) and P (43 kg P ha?1 year?1) along the study period. River export of N and P accounted for 3–27% and?~?2% of N and P soil net accumulation, respectively, while Si export was significantly greater (25 kg Si ha?1 year?1) than Si net accumulation on farmlands. The stoichiometry of net nutrient accumulation in soils was not reflected by the stoichiometry of nutrient riverine export, due to element-specific mechanisms. We speculate that N and Si vertical and horizontal mobilization is increased by the irrigation loop, while P retention is favored by limited erosion due to limited slopes in the Mincio River basin. The simultaneous analysis of N, Si and P allows us to better understand the different paths, transformation and retention mechanisms at the watershed scale. 相似文献
996.
Feasibility of a guided self‐help intervention to reduce psychological distress in South Sudanese refugee women in Uganda
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997.
Rodrigo?A.?Mendes Shawan?K.?C.?Almeida Iuri?N.?Soares Cristina?A.?Barboza Renato?G.?Freitas Alex?Brown Gabriel?L.?C.?de?SouzaEmail authorView authors OrcID profile 《Journal of molecular modeling》2018,24(6):133
In this work, we present a computational study on the antioxidant potential of myricetin 3,4\(^{\prime }\)-di-O-α-L-rhamnopyranoside (Compound M). A density functional theory (DFT) approach with the B3LYP and LC-ωPBE functionals and with both the 6-311G(d,p) and 6-311+G(d,p) basis sets was used. The focus of the investigation was on the structural and energetic parameters including both bond dissociation enthalpies (BDEs) and ionization potentials (IPs), which provide information on the potential antioxidant activity. The properties computed were compared with BDEs and IPs available in the literature for myricetin, a compound well known for presenting antioxidant activity (and the parent molecule of the compound of interest in the present work). Myricetin 3,4\(^{\prime }\)-di-O-α-L-rhamnopyranoside presented the lowest BDE to be 79.13 kcal/mol (as determined using B3LYP/6-311G(d,p) in water) while myricetin has a quite similar value (within 3.4 kcal/mol). IPs computed in the gas phase [B3LYP/6-311G(d,p)] are 157.18 and 161.4 kcal/mol for myricetin 3,4\(^{\prime }\)-di-O-α-L-rhamnopyranoside and myricetin, respectively. As the values of BDEs are considerably lower than the ones probed for IPs (in the gas phase or in any given solvent environment), the hydrogen atom transfer mechanism is preferred over the single electron transfer mechanism. The BDEs obtained suggest that myricetin 3,4\(^{\prime }\)-di-O-α-L-rhamnopyranoside can present antioxidant potential as good as the parent molecule myricetin (a well-known antioxidant). Therefore, experimental tests on the antioxidant activity of Compound M are encouraged. 相似文献
998.
Mapping Nonfullerene Acceptors with a Novel Wide Bandgap Polymer for High Performance Polymer Solar Cells
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Xunfan Liao Zhaoyang Yao Ke Gao Xueliang Shi Lijian Zuo Zonglong Zhu Lie Chen Feng Liu Yiwang Chen Alex K.‐Y. Jen 《Liver Transplantation》2018,8(24)
A new weak electron‐deficient building block, bis(2‐ethylhexyl) 2,5‐bis(5‐bromothiophen‐2‐yl) thieno[3,2‐b]thiophene‐3,6‐dicarboxylate ( TT‐Th ), is incorporated to construct a wide‐bandgap (1.88 eV) polymer PBDT‐TT for nonfullerene polymer solar cells (NF‐PSCs). PBDT‐TT possesses suitable energy levels and complementary absorption when blended with both ITIC analogues ( ITIC and IT‐M ) and a near‐infrared (NIR) acceptor ( 6TIC ). Moreover, PBDT‐TT exhibits good conjugated planarity and preferable face‐on orientation in the blended thin film, which are beneficial for charge transfer and carrier transport. The PSCs based on PBDT‐TT : IT‐M and PBDT‐TT : 6TIC blend films yield high power conversion efficiencies of 11.38% and 11.03%, respectively. To the best of the authors' knowledge, the PCE of 11.03% for PBDT‐TT : 6TIC‐ based device is one of the highest values reported for NIR NF‐PSCs. This work demonstrates that TT‐Th is a useful new electron‐accepting building block for making p‐type wide bandgap polymers for efficient NIR NF‐PSCs. 相似文献
999.
Recently, the stability of organic–inorganic perovskite thin films under thermal, photo, and moisture stresses has become a major concern for further commercialization due to the high volatility of the organic cations in the prototype perovskite composition (CH3NH3PbI3). All inorganic cesium (Cs) based perovskite is an alternative to avoid the release or decomposition of organic cations. Moreover, substituting Pb with Sn in the organic–inorganic lead halide perovskites has been demonstrated to narrow the bandgap to 1.2–1.4 eV for high‐performance perovskite solar cells. In this work, a series of CsPb1?xSnxIBr2 perovskite alloys via one‐step antisolvent method is demonstrated. These perovskite films present tunable bandgaps from 2.04 to 1.64 eV. Consequently, the CsPb0.75Sn0.25IBr2 with homogeneous and densely crystallized morphology shows a remarkable power conversion efficiency of 11.53% and a high Voc of 1.21 V with a much improved phase stability and illumination stability. This work provides a possibility for designing and synthesizing novel inorganic halide perovskites as the next generation of photovoltaic materials. 相似文献
1000.
Terthieno[3,2‐b]Thiophene (6T) Based Low Bandgap Fused‐Ring Electron Acceptor for Highly Efficient Solar Cells with a High Short‐Circuit Current Density and Low Open‐Circuit Voltage Loss
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Xueliang Shi Jingde Chen Ke Gao Lijian Zuo Zhaoyang Yao Feng Liu Jianxin Tang Alex K.‐Y. Jen 《Liver Transplantation》2018,8(12)
A terthieno[3,2‐b]thiophene ( 6T ) based fused‐ring low bandgap electron acceptor, 6TIC , is designed and synthesized for highly efficient nonfullerene solar cells. The chemical, optical, and physical properties, device characteristics, and film morphology of 6TIC are intensively studied. 6TIC shows a narrow bandgap with band edge reaching 905 nm due to the electron‐rich π‐conjugated 6T core and reduced resonance stabilization energy. The rigid, π‐conjugated 6T also offers lower reorganization energy to facilitate very low VOC loss in the 6TIC system. The analysis of film morphology shows that PTB7‐Th and 6TIC can form crystalline domains and a bicontinuous network. These domains are enlarged when thermal annealing is applied. Consequently, the device based on PTB7‐Th : 6TIC exhibits a high power conversion efficiency (PCE) of 11.07% with a high JSC > 20 mA cm?2 and a high VOC of 0.83 V with a relatively low VOC loss (≈0.55 V). Moreover, a semitransparent solar cell based on PTB7‐Th : 6TIC exhibits a relatively high PCE (7.62%). The device can have combined high PCE and high JSC is quite rare for organic solar cells. 相似文献