排序方式: 共有35条查询结果,搜索用时 78 毫秒
1.
Raza Syed Arshad Siddiqui Atiq W. Standing Craig 《Systemic Practice and Action Research》2019,32(2):125-153
Systemic Practice and Action Research - Most of the traditional technology acceptance models revolve around information systems (IS)/information technology (IT) adoption at individual user level.... 相似文献
2.
Rasmussen SG DeVree BT Zou Y Kruse AC Chung KY Kobilka TS Thian FS Chae PS Pardon E Calinski D Mathiesen JM Shah ST Lyons JA Caffrey M Gellman SH Steyaert J Skiniotis G Weis WI Sunahara RK Kobilka BK 《Nature》2011,477(7366):549-555
G protein-coupled receptors (GPCRs) are responsible for the majority of cellular responses to hormones and neurotransmitters as well as the senses of sight, olfaction and taste. The paradigm of GPCR signalling is the activation of a heterotrimeric GTP binding protein (G protein) by an agonist-occupied receptor. The β(2) adrenergic receptor (β(2)AR) activation of Gs, the stimulatory G protein for adenylyl cyclase, has long been a model system for GPCR signalling. Here we present the crystal structure of the active state ternary complex composed of agonist-occupied monomeric β(2)AR and nucleotide-free Gs heterotrimer. The principal interactions between the β(2)AR and Gs involve the amino- and carboxy-terminal α-helices of Gs, with conformational changes propagating to the nucleotide-binding pocket. The largest conformational changes in the β(2)AR include a 14 ? outward movement at the cytoplasmic end of transmembrane segment 6 (TM6) and an α-helical extension of the cytoplasmic end of TM5. The most surprising observation is a major displacement of the α-helical domain of Gαs relative to the Ras-like GTPase domain. This crystal structure represents the first high-resolution view of transmembrane signalling by a GPCR. 相似文献
3.
Coilín Boland Dianfan Li Syed Tasadaque Ali Shah Stefan Haberstock Volker Dötsch Frank Bernhard Martin Caffrey 《Cellular and molecular life sciences : CMLS》2014,71(24):4895-4910
Membrane proteins are key elements in cell physiology and drug targeting, but getting a high-resolution structure by crystallographic means is still enormously challenging. Novel strategies are in big demand to facilitate the structure determination process that will ultimately hasten the day when sequence information alone can provide a three-dimensional model. Cell-free or in vitro expression enables rapid access to large quantities of high-quality membrane proteins suitable for an array of applications. Despite its impressive efficiency, to date only two membrane proteins produced by the in vitro approach have yielded crystal structures. Here, we have analysed synergies of cell-free expression and crystallisation in lipid mesophases for generating an X-ray structure of the integral membrane enzyme diacylglycerol kinase to 2.28-Å resolution. The quality of cellular and cell-free-expressed kinase samples has been evaluated systematically by comparing (1) spectroscopic properties, (2) purity and oligomer formation, (3) lipid content and (4) functionality. DgkA is the first membrane enzyme crystallised based on cell-free expression. The study provides a basic standard for the crystallisation of cell-free-expressed membrane proteins and the methods detailed here should prove generally useful and contribute to accelerating the pace at which membrane protein structures are solved. 相似文献
4.
5.
Amanullah A Azam N Balliet A Hollander C Hoffman B Fornace A Liebermann D 《Nature》2003,424(6950):741; discussion 742
6.
Syed Furqan Rafique Jianhua Zhang Muhammad Hanan Waseem Aslam Atiq Ur Rehman Zmarrak Wali Khan 《清华大学学报》2018,(3)
This study provides details of the energy management architecture used in the Goldwind microgrid test bed. A complete mathematical model, including all constraints and objectives, for microgrid operational management is first described using a modified prediction interval scheme. Forecasting results are then achieved every 10 min using the modified fuzzy prediction interval model, which is trained by particle swarm optimization.A scenario set is also generated using an unserved power profile and coverage grades of forecasting to compare the feasibility of the proposed method with that of the deterministic approach. The worst case operating points are achieved by the scenario with the maximum transaction cost. In summary, selection of the maximum transaction operating point from all the scenarios provides a cushion against uncertainties in renewable generation and load demand. 相似文献
7.
ZnO and Cr-doped ZnO thin films are grown on to glass substrates using reactive electron beam(e-beam) evaporation technique.Variation of structural,morphological,and optical properties with Cr doping is investigated.X-ray diffraction(XRD) studies show that the films are polycrystalline in nature with single phase.Energy dispersive spectroscopy(EDS) results demonstrate that Cr ions are substitutionally incorporated into ZnO.Atomic force microscopy(AFM) reveals that the films present a compact surface and root mean squared(RMS) roughness increased with Cr contents.The optical band gap energy Eg of the films has been determined using Transmission data by spectrophotometer and ellipsometry.The band gap energy found to be decreased with increasing Cr doping concentration.The optical constants(refractive index,extinction coefficient) are calculated using ellipsometry and found to increase with Cr doping concentration. 相似文献
8.
论述了从塞拉利昂不同地区采集的6个粘土试样的一些物理性能,这些物理性能与无釉烧结地砖的耐压强度有一定的关系。由相关系数可知,烧结温度是控制地砖强度的主要因素,虽然粘土的粒度分布与地砖强度之间无明显关系,但过多添加砂子会降低砖的强度,而适当的粘土和淤泥则提高砖的强度。高塑性有降低砖强度的作用,体积密度和气孔率对强度有相反的影响,前者能提高强度,而后者则会降低砖的强度。 相似文献
9.
Syeda Sohaila Naz Muhammad Raza Shah Nazar Ul Islam Syed Sartaj Alam 《自然科学进展(英文版)》2019,29(2):129-137
Medically, bacterial ureases are important virulent factors and are used for treatment of peptic ulcers and urinary tones. Reported urease inhibitors are associated with various side effects including antibiotic resistance as a major one. Still there is an urgent need to synthesize new urease inhibitors. In this context we have synthesized new urease inhibitor i.e. AgL that is composed of Ag nanomaterials capped with N-substituted methyl 5-acetamido-β-resorcylate(L). The conjugation of L to silver was confirmed through FTIR, UV–vis and TEM analysis.Bare silver nanomaterials(Ag) were also prepared. The stability of AgL nanostructures was determined against various parameters(temperature, high salt concentration, pH) and found to be stable. The in vitro antimicrobial(antibacterial, antifungal), enzyme inhibition(xanthine oxidase, urease, carbonic anhydrase, α-chymotrypsin,cholinesterase) and antioxidant activities of AgL were investigated and compared with Ag, L and standard drugs.In comparison to other bioactivities, AgL shows statistically enhanced selective enzyme inhibition activity against urease enzyme. Urease inhibition activity of AgL was significantly greater than standard drug(thiourea),L and Ag. On a per weight basis, AgL required about 11–18 times less amount of L for inhibition of urease enzyme. 相似文献
10.
Change or innovation diffusion is a key issue for most business organizations but is yet difficult to implement as the change
management process is often complex as it relies on an organized methodology to complement an organization’s commitment and
participation. An ambiguous environment surrounding change mechanism tends to develop unintended attitudes, resulting in resistance
and conflict. The study proposes a model for the management of such conflicts among change participants (involved and affected)
in the context of organizational change. The authors consider organizational change process as an innovation project that
treats change and conflicts holistically with the Ulrich’s notion of boundary considerations (boundary critique). A social
network setting of multiple stakeholders is considered to effectively help in resolving problematic situations that hinder
organizational learning and change. The proposed model provides a theoretical foundation based on concepts governing Critical
Systems Heuristics (CSH), change theory, stakeholder theory and conflict management. 相似文献