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1.
Summary. The reconstruction index of all semiregular permutation groups is determined. We show that this index satisfies 3 £ r(G, W) £ 5 3 \leq \rho(G, \Omega) \leq 5 and we classify the groups in each case. 相似文献
2.
3.
Heredia KL Bontempo D Ly T Byers JT Halstenberg S Maynard HD 《Journal of the American Chemical Society》2005,127(48):16955-16960
Protein-polymer conjugates are widely used in biotechnology and medicine, and new methods to prepare the bioconjugates would be advantageous for these applications. In this report, we demonstrate that bioactive "smart" polymer conjugates can be synthesized by polymerizing from defined initiation sites on proteins, thus preparing the polymer conjugates in situ. In particular, free cysteines, Cys-34 of bovine serum albumin (BSA) and Cys-131 of T4 lysozyme V131C, were modified with initiators for atom transfer radical polymerization (ATRP) either through a reversible disulfide linkage or irreversible bond by reaction with pyridyl disulfide- and maleimide-functionalized initiators, respectively. Initiator conjugation was verified by electrospray-ionization mass spectroscopy (ESI-MS), and the location of the modification was confirmed by muLC-MSMS (tandem mass spectrometry) analysis of the trypsin-digested protein macroinitiators. Polymerization of N-isopropylacrylamide (NIPAAm) from the protein macroinitiators resulted in thermosensitive BSA-polyNIPAAm and lysozyme-polyNIPAAm in greater than 65% yield. The resultant conjugates were characterized by gel electrophoresis and size exclusion chromatography (SEC) and easily purified by preparative SEC. The identity of polymer isolated from the BSA conjugate was confirmed by (1)H NMR, and the polydispersity index was determined by gel permeation chromatography (GPC) to be as low as 1.34. Lytic activities of the lysozyme conjugates were determined by two standard assays and compared to that of the unmodified enzyme prior to polymerization; no statistical differences in bioactivity were observed. 相似文献
4.
Masuda J Maynard DM Nishimura M Ueda T Kowalak JA Markey SP 《Journal of chromatography. A》2005,1063(1-2):57-69
A one- or two-dimensional high performance liquid chromatography system for electrospray ionization mass spectrometers has been developed that is optimized for ion exchange and reversed phase separations. A unique and simple valve configuration permits the use of a variety of non-volatile salts; ammonium sulfate was used in an example of strong cation exchange separations. The system was designed and evaluated for both micro- and nanoflow chromatography. The peptide detection limit was approximately 100 fmol for micro- and 20 fmol for nanoflow, demonstrating the concentration and mass sensitivity improvements expected with nanoelectrospray ionization. The 1D/2D-HPLC MS system is fully automated for routine peptide analyses, compatible with direct injection of proteolytic digests, and exhibits chromatographic reproducibility and sensitivity. Software permits operator selection of either a 1D or 2D configuration with corresponding system parameters as required for individual samples. The hardware elements and resulting performance are described in this paper. 相似文献
5.
Darensbourg DJ Maynard EL Holtcamp MW Klausmeyer KK Reibenspies JH 《Inorganic chemistry》1996,35(9):2682-2684
6.
Heredia KL Tao L Grover GN Maynard HD 《Journal of polymer science. Part A, Polymer chemistry》2010,1(2):168-170
A heterotelechelic biotin-maleimide polymer containing a cleavable disulfide bond was synthesized by RAFT polymerization and used to reversibly modify surfaces with proteins. 相似文献
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8.
We develop a self-consistent theory of temporal fluctuations of a speckle pattern resulting from the multiple scattering of a coherent wave in a weakly nonlinear disordered medium. The speckle pattern is shown to become unstable if the nonlinearity exceeds a threshold value. The instability is due to a feedback provided by the multiple scattering and manifests itself in spontaneous fluctuations of the scattered intensity. The development of instability is independent of the sign of nonlinearity. 相似文献
9.
Phospholipid lung surfactant and nanoparticle surface toxicity: Lessons from diesel soots and silicate dusts 总被引:3,自引:0,他引:3
William E. Wallace Michael J. Keane David K. Murray William P. Chisholm Andrew D. Maynard Tong-man Ong 《Journal of nanoparticle research》2007,9(1):23-38
Because of their small size, the specific surface areas of nanoparticulate materials (NP), described as particles having at
least one dimension smaller than 100 nm, can be large compared with micrometer-sized respirable particles. This high specific
surface area or nanostructural surface properties may affect NP toxicity in comparison with micrometer-sized respirable particles
of the same overall composition. Respirable particles depositing on the deep lung surfaces of the respiratory bronchioles
or alveoli will contact pulmonary surfactants in the surface hypophase. Diesel exhaust ultrafine particles and respirable
silicate micrometer-sized insoluble particles can adsorb components of that surfactant onto the particle surfaces, conditioning
the particles surfaces and affecting their in vitro expression of cytotoxicity or genotoxicity. Those effects can be particle surface composition-specific. Effects of particle
surface conditioning by a primary component of phospholipid pulmonary surfactant, diacyl phosphatidyl choline, are reviewed
for in vitro expression of genotoxicity by diesel exhaust particles and of cytotoxicity by respirable quartz and aluminosilicate kaolin
clay particles. Those effects suggest methods and cautions for assaying and interpreting NP properties and biological activities. 相似文献
10.
Measuring particle size-dependent physicochemical structure in airborne
single walled carbon nanotube agglomerates 总被引:1,自引:1,他引:1
Andrew D. Maynard Bon Ki Ku Mark Emery Mark Stolzenburg Peter H. McMurry 《Journal of nanoparticle research》2007,9(1):85-92
As-produced single-walled carbon nanotube (SWCNT) material is a complex matrix of carbon nanotubes, bundles of nanotubes (nanoropes),
non-tubular carbon and metal catalyst nanoparticles. The pulmonary toxicity of material released during manufacture and handling
will depend on the partitioning and arrangement of these components within airborne particles. To probe the physicochemical
structure of airborne SWCNT aggregates, a new technique was developed and applied to aerosolized as-produced material. Differential
Mobility Analysis-classified aggregates were analyzed using an Aerosol Particle Mass Monitor, and a structural parameter Γ
(proportional to the square of particle mobility diameter, divided by APM voltage) derived. Using information on the constituent
components of the SWCNT, modal values of Γ were estimated for specific particle compositions and structures, and compared
against measured values. Measured modal values of Γ for 150 nm mobility diameter aggregates suggested they were primarily
composed of non-tubular carbon from one batch of material, and thin nanoropes from a second batch of material – these findings
were confirmed using Transmission Electron Microscopy. Measured modal values of Γ for 31 nm mobility diameter aggregates indicated
that they were comprised predominantly of thin carbon nanoropes with associated nanometer-diameter metal catalyst particles;
there was no indication that either catalyst particles or non-tubular carbon particles were being preferentially released
into the air. These results indicate that the physicochemistry of aerosol particles released while handling as-produced SWCNT
may vary significantly by particle size and production batch, and that evaluations of potential health hazards need to account
for this.
Disclaimer: The mention of any company or product does not constitute an endorsement by the Centers for Disease Control and
Prevention. The findings and conclusions in this paper are those of the authors and do not necessarily represent the views
of the National Institute for Occupational Safety and Health. 相似文献