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71.
Philipp Leippe Johannes Broichhagen Katia Cailliau Alexandra Mougel Marion Morel Colette Dissous Dirk Trauner Jrme Vicogne 《Angewandte Chemie (International ed. in English)》2020,59(17):6720-6723
Receptor tyrosine kinases (RTKs) are key regulators of cellular functions in metazoans. In vertebrates, RTKs are mostly activated by polypeptides but are not naturally sensitive to amino acids or light. Taking inspiration from Venus kinase receptors (VKRs), an atypical family of RTKs found in nature, we have transformed the human insulin (hIR) and hepatocyte growth factor receptor (hMET) into glutamate receptors by replacing their extracellular binding domains with the ligand‐binding domain of metabotropic glutamate receptor type 2 (mGluR2). We then imparted light sensitivity through covalent attachment of a synthetic glutamate‐based photoswitch via a self‐labelling SNAP tag. By employing a Xenopus laevis oocyte kinase activity assay, we demonstrate how these chimeric RTKs, termed light‐controlled human insulin receptor (LihIR) and light‐controlled human MET receptor (LihMET), can be used to exert optical control over the insulin or MET signaling pathways. Our results outline a potentially general strategy to convert RTKs into photoreceptors. 相似文献
72.
Angelo Alberti Massimo Benaglia Hanns Fischer Maurizio Guerra Michele Laus Dante Macciantelli Almar Postma Katia Sparnacci 《Helvetica chimica acta》2006,89(10):2103-2118
The reversible‐addition‐fragmentation chain transfer (RAFT) controlled radical polymerization of such vinylic monomers as styrene (= ethenylbenzene) has gained increasing popularity in current years. While there is a general agreement on the mechanism of RAFT polymerization, there is an ongoing debate about the values of the rate constants of its key steps, i.e., the addition of the propagating radicals to the mediator and the fragmentation of the resulting spin adducts. By carrying out an ESR spectroscopic investigation of the AIBN‐initiated polymerization of styrene (AIBN = 2,2′‐azobis[2‐methylpropanenitrile]), mediated by benzyl (diethoxyphosphoryl)dithioformate ( 5 ) as RAFT agent, we were able to detect and characterize four different radical species involved in the process. By reproducing their concentration–time profiles through a kinetic model, the addition and fragmentation rate constants at 90° of the propagating radicals to and from the mediator were estimated to be ca.107 M ?1 s?1 and ca. 103 s?1, respectively. The validity of the kinetic model was supported by hybrid meta DFT calculations with the BB1K functional that predicted addition‐ and fragmentation‐rate‐constant values in good agreement with those estimated from the ESR experiments. 相似文献
73.
Viviana Scognamiglio Gianni Pezzotti Ittalo Pezzotti Juan Cano Katia Buonasera Daniela Giannini Maria Teresa Giardi 《Mikrochimica acta》2010,170(3-4):215-225
Biosensors are projected to find many applications due to their high selectivity and sensitivity, rapid reaction, economy and ease of handling in field measurements. Even though biosensors for a wide range of environmental pollutants have been extensively reported in the literature, the decision to develop a suitable biosensing system that can be approved by a regulatory perspective for environmental applications is fraught with technical issues. These issues mainly concern the biological recognition element, the physico-chemical transducer and the interfaces between the biological and the physical components, but also aspects of fluidics, electronics, and software for data processing. This article reviews methods together with a process to move biosensor technology from research laboratories to market, focusing as a case in point on challenges and possible opportunities in the development of photosynthetic-based biosensors for environmental applications. 相似文献
74.
Lilian R. Avila Emerson H. de Faria Katia J. Ciuffi Eduardo J. Nassar Paulo S. Calefi Miguel A. Vicente Raquel Trujillano 《Journal of colloid and interface science》2010,341(1):186-193
Functionalization of Brazilian São Simão kaolinite and Spanish Yunclillos saponite with the alkoxysilanes 3-aminopropyltriethoxysilane and 3-mercaptopropyltrimethoxysilane is reported. The resulting hybrids were characterized by X-ray diffraction, thermal analysis, infrared absorption spectroscopy, and scanning electron microscopy, which demonstrated the effectiveness of the interlamellar grafting process. The X-ray diffractograms revealed incorporation of the alkoxide molecules into the interlayer space of the clays. The displacement of the stretching bands of interlayer hydroxyls in the infrared spectra of the modified kaolinites and the increased intensity of the Mg–OH vibrations in the spectra of the modified saponites confirmed the functionalization of the clays. The thermal behavior of the organoclays confirmed the stability of the hybrids, which was dependent on the clay used for preparation of the materials. 相似文献
75.
76.
Ananias Sandra R. Mauro Antonio E. Zutin Katia Picchi Cristina M.C. Santos Regina H.A. 《Transition Metal Chemistry》2004,29(3):284-290
The cyanate-bridged cyclopalladated compound [Pd(N,C-dmba)(-NCO)]2
(1)(dmba = PhCH2NMe2) reacts in CH2Cl2 with 2,3-lutidine (2,3-lut), 3,4-lutidine (3,4-lut), 2,2-bipyridine (2,2-bipy) and 4,4-bipyridine (4,4-bipy), to give [Pd(N,C-dmba)(NCO)(2,3-lut)](2), [Pd(N,C-dmba)(NCO)(3,4-lut)](3), [{Pd(N,C-dmba)(NCO)}2(-2,2-bipy)]· CH2Cl2
(4) and [{Pd(N,C-dmba)(NCO)}2(-4,4-bipy)]· CH2Cl2
(5), respectively. The compounds were characterized by elemental analysis, i.r. and n.m.r. spectroscopy and also by t.g.a. The i.r. spectra of (2–5) display typical bands of monodentate N-bonded cyanate groups, whereas the n.m.r. data of (4) are consistent with the presence of a bridging 2,2-bipyridine ligand. Complex (4) decomposes slowly in acetone. One of the products formed, [Pd(H2CCOMe)Cl(2,2-bipy)](6), was characterized by X-ray diffraction. As inferred from the t.g.a., the thermal stability decreases in the order:[{Pd(N,C-dmba)(NCO)}2(-4,4-bipy)].CH2Cl2
(5) > [Pd(N,C-dmba)(2,3-lut)(NCO)](2)=[Pd(N,C-dmba)(3,4-lut)(NCO)](3) > [{Pd(N,C-dmba)(NCO)}2(-2,2-bipy)]· CH2Cl2
(4). According to thermal analysis and X-ray diffraction patterns compounds (2–3) decompose into metallic palladium Pd(0), whereas (4–5) decompose with the formation of PdO. The X-ray crystal and molecular structure of [Pd(N,C-dmba)(NCO)(2,3-lut)](2) was determined. The lutidine unit is perpendicular to the coordination plane. 相似文献
77.
Dirk C. de Graaf Wolfgang Ritter Frans J. Jacobs Marleen Brunain Hein Imberechts Koen Mintiens Yves Van der Stede Bart Verheyden Aud Kari Fauske Patrick Boujon Gabriela Chioveanu Daniel Dezmirean Giovanni Formato Franco Mutinelli Hendrik-Jan Roest Dalibor Titĕra Stephen F. Pernal Katia Knapen 《Accreditation and quality assurance》2009,14(5):273-276
We report on the first proficiency test in the context of honey bee disease testing on a broad international scale. Honey
samples were distributed to 12 participating laboratories for isolation and identification of spores of the etiological agent
of American foulbrood, Paenibacillus larvae. Of the 11 laboratories responding to this proficiency testing event, only 6 (54%) provided data that were in full agreement
with the previously determined status of the honey samples; eight (72%) laboratories fell within the threshold for qualification
as defined a priori in this proficiency test (=level of agreement of at least 90%). Some lessons can now be drawn from the
organizational point of view and will certainly improve new initiatives to be taken. 相似文献
78.
Cover Picture: Viologen‐Templated Arrays of Cucurbit[7]uril‐Modified Iron‐Oxide Nanoparticles (Chem. Eur. J. 12/2015) 下载免费PDF全文
79.
Dr. Farah Benyettou Dr. Katia Nchimi‐Nono Dr. Mustapha Jouiad Dr. Yoann Lalatonne Dr. Irena Milosevic Prof. Laurence Motte Prof. John‐Carl Olsen Prof. Na'il Saleh Prof. Ali Trabolsi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(12):4607-4613
Magnetic and fluorescent assemblies of iron‐oxide nanoparticles (NPs) were constructed by threading a viologen‐based ditopic ligand, DPV2+, into the cavity of cucurbituril (CB[7]) macrocycles adsorbed on the surface of the NPs. Evidence for the formation of 1:2 inclusion complexes that involve DPV2+ and two CB[7] macrocycles was first obtained in solution by 1H NMR and emission spectroscopy. DPV2+ was found to induce self‐assembly of nanoparticle arrays (DPV2+?CB[7]NPs) by bridging CB[7] molecules on different NPs. The resulting viologen‐crosslinked iron‐oxide nanoparticles exhibited increased saturation magnetization and emission properties. This facile supramolecular approach to NP self‐assembly provides a platform for the synthesis of smart and innovative materials that can achieve a high degree of functionality and complexity and that are needed for a wide range of applications. 相似文献
80.
Katia Barbera Leone Frusteri Giuseppe Italiano Lorenzo Spadaro Francesco Frusteri Siglinda Perathoner Gabriele Centi 《催化学报》2014,35(6):869-876
The investigation by SEM/TEM, porosity, and X-ray diffraction measurements of the graphitization process starting from amorphous carbon nanospheres, prepared by glucose carbonization, is reported. Aspects studied are the annealing temperature in the 750–1000 °C range, the type of inert carrier gas, and time of treatment in the 2–6 h range. It is investigated how these parameters influence the structural and morphological characteristics of the carbon materials obtained as well as their nanostructure. It is shown that it is possible to maintain after graphitization the round-shaped macro morphology, a high surface area and porosity, and especially a large structural disorder in the graphitic layers stacking, with the presence of rather small ordered domains. These are characteristics interesting for various catalytic applications. The key in obtaining these characteristics is the thermal treatment in a flow of N2. It was demonstrated that the use of He rather than N2 does not allow obtaining the same results. The effect is attributed to the presence of traces of oxygen, enough to create the presence of oxygen functional groups on the surface temperatures higher than 750 °C, when graphitization occurs. These oxygen functional groups favor the graphitization process. 相似文献