安全高效矿井监控关键技术研究

提出安全高效矿井应采用先进可靠的监控技术,实现供电、排水、通风、压风、运输、提升、瓦斯抽采等固定岗位无人值守和地面远程控制,综采、综放等采煤工作面少人作业和地面远程控制;提出供电、排水、通风、压风、运输、提升、瓦斯抽采等监控系统应具有地面远程控制功能;提出具有远程控制、报警联动、调度指挥等功能的煤矿调度指挥控制中心;提出整合计算机网络机房、程控交换机机房、调度交换机机房、监控系统机房等的数据中心;提出基于煤层瓦斯压力和瓦斯含量、综合指标、钻屑瓦斯解吸指标、复合指标、R值指标、瓦斯涌出量(根据瓦斯体积分数和风量计算)、巷道位置、微震、地音、温度等及其变化的煤与瓦斯突出预警方法;提出基于WiFi的矿用无线传输接口,以便于互通互联;提出通过分布式光纤测温预警煤炭自然发火,较通过监测CO等煤炭自然发火标志气体更直接、更及时、更可靠;提出根据运煤量实时调整输送带速度:当煤量较小时降低输送带运行速度,当煤量较大时提高输送带运行速度,以提高运输效率,减少设备磨损;提出基于光纤综合保护的供电监控系统具有防越级跳闸、地面远程整定和地面远程控制功能,提高了煤矿供电的可靠性,可实现煤矿井下机电硐室无人值守;提出具有煤岩识别与滚筒自动调高,采煤机、刮板机、液压支架3机联动,记忆割煤,地面远程、顺槽近程、手动控制和紧急停机,放顶煤量和煤矸控制,采煤机和刮板机等大型机电设备故障诊断等功能的采煤工作面监控系统。     

基于蚁群优化的WSN能耗均衡链状路由协议

为了从路由技术的角度解决无线传感器网络的能耗问题,综合蚁群优化算法和PEGASIS协议的思想提出了ACO-PEGASIS路由协议;该协议采用蚁群优化算法构建通信链,解决了PEGASIS协议中由于贪婪算法的局部性产生的相邻节点间的长链问题;并在成链过程中综合考虑节点间距离、节点剩余能量等因子,以均衡全网的能量消耗;同时根据距离和能量因素选取链头节点并采用一定措施降低链头重选次数;仿真结果表明,与PEGASIS协议相比,该协议更加有效地均衡了全网的能量消耗,延长了网络的生存周期。     

铸态及快淬态无钴AB5型贮氢合金的循环稳定性

对AB5型LaxMm1-x(NiMnSiAlFe)49(x=0,0.45,0.75,1.00,摩尔分数)贮氢合金进行了快淬处理,研究了La含量及快淬工艺对合金微观结构及电化学循环稳定性的影响.结果表明:La含量的增加对铸态合金的循环稳定性没有明显影响,但使快淬态合金的循环稳定性下降,且快淬处理能显著提高合金的循环稳定性.当La替代量从0增加到1.00时,经300次充放循环后,铸态合金的容量保持率(Rh)从59.2%增加到59.8%;16 m/s淬速快淬态合金的容量保持率从83.9%下降到65.0%.对于x=0.45的合金,当淬速从0(铸态被定义为淬速等于0)增加到28 m/s时,容量保持率从59.8%增加到75.8%.     

OsMre11 Is Required for Mitosis during Rice Growth and Development

Meiotic recombination 11 (Mre11) is a relatively conserved nuclease in various species. Mre11 plays important roles in meiosis and DNA damage repair in yeast, humans and Arabidopsis, but little research has been done on mitotic DNA replication and repair in rice. Here, it was found that Mre11 was an extensively expressed gene among the various tissues and organs of rice, and loss-of-function of Mre11 resulted in severe defects of vegetative and reproductive growth, including dwarf plants, abnormally developed male and female gametes, and completely abortive seeds. The decreased number of cells in the apical meristem and the appearance of chromosomal fragments and bridges during the mitotic cell cycle in rice mre11 mutant roots revealed an essential role of OsMre11. Further research showed that DNA replication was suppressed, and a large number of DNA strand breaks occurred during the mitotic cell cycle of rice mre11 mutants. The expression of OsMre11 was up-regulated with the treatment of hydroxyurea and methyl methanesulfonate. Moreover, OsMre11 could form a complex with OsRad50 and OsNbs1, and they might function together in non-homologous end joining and homologous recombination repair pathways. These results indicated that OsMre11 plays vital roles in DNA replication and damage repair of the mitotic cell cycle, which ensure the development and fertility of rice by maintaining genome stability.     

Platelet-Rich Plasma Promotes the Proliferation of Human Keratinocytes via a Progression of the Cell Cycle. A Role of Prolidase

Although the role of platelet-rich plasma (PRP) in tissue regeneration has been confirmed in many studies, the mechanism of this process is still not fully understood. Human keratinocytes (HaCaT) cells were used as an experimental model for studies on the effects of PRP on cell proliferation, migration, collagen biosynthesis, prolidase activity, and its expression and anabolic signaling. The activation of epidermal growth factor receptor (EGFR), β₁-integrin, and insulin-like growth factor-1 receptor (IGF-1R) by PRP were investigated by western blot and immunocytochemistry. It has been found that PRP induced keratinocytes migration and proliferation through activation of cell cycle progression and EGFR downstream signaling. Similar biological effects were achieved by an addition to the culture medium of prolidase (PEPD), a ligand of EGFR (PRP is a rich source of PEPD–2 ng/mL). PRP-dependent stimulation of collagen biosynthesis was accompanied by an increase in the expression of NF-κβ, IGF-1R-downstream signaling proteins, and PEPD activity. The data suggest that PRP activates a complex of growth factors and adhesion receptors that stimulate cell proliferation, migration, and collagen biosynthesis. PRP induces PEPD-dependent human keratinocyte proliferation through activation of the EGFR receptor. Our study provides a novel mechanism of PRP-dependent wound healing.     

Inhibitors of Cyclin-Dependent Kinases: Types and Their Mechanism of Action

Recent studies on cyclin-dependent kinase (CDK) inhibitors have revealed that small molecule drugs have become very attractive for the treatment of cancer and neurodegenerative disorders. Most CDK inhibitors have been developed to target the ATP binding pocket. However, CDK kinases possess a very similar catalytic domain and three-dimensional structure. These features make it difficult to achieve required selectivity. Therefore, inhibitors which bind outside the ATP binding site present a great interest in the biomedical field, both from the fundamental point of view and for the wide range of their potential applications. This review tries to explain whether the ATP competitive inhibitors are still an option for future research, and highlights alternative approaches to discover more selective and potent small molecule inhibitors.     

Post-Translational Modifications of Retroviral HIV-1 Gag Precursors: An Overview of Their Biological Role

Protein post-translational modifications (PTMs) play key roles in eukaryotes since they finely regulate numerous mechanisms used to diversify the protein functions and to modulate their signaling networks. Besides, these chemical modifications also take part in the viral hijacking of the host, and also contribute to the cellular response to viral infections. All domains of the human immunodeficiency virus type 1 (HIV-1) Gag precursor of 55-kDa (Pr55^Gag), which is the central actor for viral RNA specific recruitment and genome packaging, are post-translationally modified. In this review, we summarize the current knowledge about HIV-1 Pr55^Gag PTMs such as myristoylation, phosphorylation, ubiquitination, sumoylation, methylation, and ISGylation in order to figure out how these modifications affect the precursor functions and viral replication. Indeed, in HIV-1, PTMs regulate the precursor trafficking between cell compartments and its anchoring at the plasma membrane, where viral assembly occurs. Interestingly, PTMs also allow Pr55^Gag to hijack the cell machinery to achieve viral budding as they drive recognition between viral proteins or cellular components such as the ESCRT machinery. Finally, we will describe and compare PTMs of several other retroviral Gag proteins to give a global overview of their role in the retroviral life cycle.     

Synthesis and Pharmacological In Vitro Investigations of Novel Shikonin Derivatives with a Special Focus on Cyclopropane Bearing Derivatives

Melanoma is the deadliest form of skin cancer and accounts for about three quarters of all skin cancer deaths. Especially at an advanced stage, its treatment is challenging, and survival rates are very low. In previous studies, we showed that the constituents of the roots of Onosma paniculata as well as a synthetic derivative of the most active constituent showed promising results in metastatic melanoma cell lines. In the current study, we address the question whether we can generate further derivatives with optimized activity by synthesis. Therefore, we prepared 31, mainly novel shikonin derivatives and screened them in different melanoma cell lines (WM9, WM164, and MUG-Mel2 cells) using the XTT viability assay. We identified (R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl 2-cyclopropyl-2-oxoacetate as a novel derivative with even higher activity. Furthermore, pharmacological investigations including the ApoToxGlo^TM Triplex assay, LDH assay, and cell cycle measurements revealed that this compound induced apoptosis and reduced cells in the G1 phase accompanied by an increase of cells in the G2/M phase. Moreover, it showed hardly any effects on the cell membrane integrity. However, it also exhibited cytotoxicity against non-tumorigenic cells. Nevertheless, in summary, we could show that shikonin derivatives might be promising drug leads in the treatment of melanoma.     

焊接构造对T型接头超低周疲劳性能的影响

为了研究焊接细节对钢结构超低周疲劳性能的影响,以T型接头为对象,在通用有限元程序Abaqus平台上,开发基于Arlequin算法的结构多尺度计算程序. 利用多尺度算法,开展焊接接头的局部弹塑性有限元分析. 比较焊趾半径、厚钢板未熔透长度及焊趾表面凹凸对局部塑性应变履历的影响,利用Coffin-Manson模型对T型接头的超低周疲劳特性进行定性讨论. 数值计算结果表明,焊趾位置是焊接接头的超低周疲劳易损位置,厚钢板的未熔透长度对焊接部位局部塑性应变的影响不大;焊趾半径对焊趾局部塑性应变有较大的影响,增大焊趾半径可以有效提升钢结构在循环荷载下的超低周疲劳性能;焊趾表面的平整性是影响焊趾局部塑性应变履历的重要因素,尖锐的凹坑会明显降低焊接接头的超低周疲劳性能,磨平的焊趾表面可以减少局部塑性应变,提高接头的超低周疲劳强度.