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71.
We wish to report synthesis of perfluorinated functionalized, branched ethers from their hydrocarbon analogues by direct fluorination. Yields up to 90%, with high purities, have been obtained at ambient temperature and pressure. This technique will likely develop into a new general method for producing perfluorinated, hyperbranched and dendritic polymers. 相似文献
72.
73.
Trends in microRNA detection 总被引:1,自引:0,他引:1
MicroRNAs (miRNAs) are short, ~22 nucleotide length RNAs that perform gene regulation. Recently, miRNA has been shown to be
linked with the onset of cancer and other diseases based on miRNA expression levels. It is important, therefore, to understand
miRNA function as it pertains to disease onset; however, in order to fully understand miRNA’s role in a disease, it is necessary
to detect the expression levels of these small molecules. The most widely used miRNA detection method is Northern blotting,
which is considered as the standard of miRNA detection methods. This method, however, is time-consuming and has low sensitivity.
This has led to an increase in the amount of detection methods available. These detection methods are either solid phase,
occurring on a solid support, or solution phase, occurring in solution. While the solid-phase methods are adaptable to high-throughput
screening and possess higher sensitivity than Northern blotting, they lack the ability for in vivo use and are often time-consuming.
The solution-phase methods are advantageous in that they can be performed in vivo, are very sensitive, and are rapid; however,
they cannot be applied in high-throughput settings. Although there are multiple detection methods available, including microarray
technology, luminescence-based assays, electrochemical assays, etc., there is still much work to be done regarding miRNA detection.
The current gaps of miRNA detection include the ability to perform multiplex, sensitive detection of miRNA with single-nucleotide
specificity along with the standardization of these new methods. Current miRNA detection methods, gaps in these methods, miRNA
therapeutic options, and the future outlook of miRNA detection are presented here. 相似文献
74.
Michael T. Crimmins Prof. J. Michael Ellis Dr. Kyle A. Emmitte Dr. Pamela A. Haile Dr. Patrick J. McDougall Dr. Jonathan D. Parrish Dr. J. Lucas Zuccarello Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(36):9223-9234
Brevetoxin A is a decacyclic ladder toxin that possesses 5‐, 6‐, 7‐, 8‐, and 9‐membered oxacycles, as well as 22 tetrahedral stereocenters. Herein, we describe a unified approach to the B, E, G, and J rings based upon a ring‐closing metathesis strategy from the corresponding dienes. The enolate technologies developed in our laboratory allowed access to the precursor acyclic dienes for the B, E, and G medium‐ring ethers. The strategies developed for the syntheses of these four monocycles ultimately provided multigram quantities of each of the rings, supporting our efforts toward the completion of a convergent synthesis of brevetoxin A. 相似文献
75.
Kyle W. Hukari Kamlesh D. Patel Ronald F. Renzi Jay A. A. West 《Electrophoresis》2010,31(16):2804-2812
Rapid and specific characterization of bacterial endospores is dependent on the ability to rupture the cell wall to enable analysis of the intracellular components. In particular, bacterial spores from the bacillus genus are inherently robust and very difficult to lyze or solubilize. Standard protocols for spore inactivation include chemical treatment, sonication, pressure, and thermal lysis. Although these protocols are effective for the inactivation of these agents, they are less well suited for sample preparation for analysis using proteomic and genomic approaches. To overcome this difficulty, we have designed a simple capillary device to perform thermal lysis of bacterial spores. Using this device, we were able to super heat (195°C) an ethylene glycol lysis buffer to perform rapid flow‐through rupture and solubilization of bacterial endospores. We demonstrated that the lysates from this preparation method are compatible with CGE as well as DNA amplification analysis. We further demonstrated the flow‐through lysing device could be directly coupled to a miniaturized electrophoresis instrument for integrated sample preparation and analysis. In this arrangement, we were enabled to perform sample lysis, fluorescent dye labeling, and protein electrophoresis analysis of bacterial spores in less than 10 min. The described sample preparation device is rapid, simple, inexpensive, and easily integratable with various microfluidic devices. 相似文献
76.
Magnetic field-controlled microfluidic transport. 总被引:1,自引:0,他引:1
Kyle M Grant Jared W Hemmert Henry S White 《Journal of the American Chemical Society》2002,124(3):462-467
Several new forms of magnetohydrodynamic (MHD) flow occurring in the solution gap between two 250-microm-diameter Pt microdisk electrodes, oriented in a face-to-face geometry and immersed in a uniform magnetic field (1 T), are described. The MHD flow results from the Lorentz force generated by diffusion of electrochemically generated molecular ions through the magnetic field. Individual microscopic flow tubes ( approximately 50-microm radius) spanning the gap between the face-to-face electrodes are observed during the 1-e(-) reduction of nitrobenzene in acetonitrile solutions. The flow tubes extend up to approximately 2 cm in length and are stable for indefinite periods. Directional transport of the electrogenerated nitrobenzene radical anion over macroscopic distances within the flow tubes, with minimal diffusional broadening, is demonstrated using an ultramicroelectrode probe to map the convective flux of redox species. Pulsed MHD transport of small packets of molecules and the formation of large area (approximately 3 cm(2)), microscopically thin (25 microm) rotating sheets of solution are also demonstrated. The results suggest that electrochemical methods, in combination with magnetohydrodynamic principles, may be useful for external field-controlled microfluidic systems. 相似文献
77.
Yan B Collins N Wheatley J Irving M Leopold K Chan C Shornikov A Fang L Lee A Stock M Zhao J 《Journal of combinatorial chemistry》2004,6(2):255-261
We have developed a high-throughput purification system to purify combinatorial libraries at a 50-100-mg scale with a throughput of 250 samples/instrument/day. We applied an accelerated retention window method to shorten the purification time and targeted one fraction per injection to simplify data tracking, lower QC workload, and simplify the postpurification processing. First, we determined the accurate retention time and peak height for all compounds using an eight-channel parallel LC/UV/MS system, and calculated the specific preparative HPLC conditions for individual compounds. The preparative HPLC conditions include the compound-specific gradient segment for individual compounds with a fixed gradient slope and the compound-specific UV or ELSD threshold for triggering a fraction collection device. A unique solvent composition or solvent strength was programmed for each compound in the preparative HPLC in order to elute all compounds at the same target time. Considering the possible deviation of the predicted retention time, a 1-min window around the target time was set to collect peaks above a threshold based on UV or ELSD detection. Dual column preparative instruments were used to maximize throughput. We have purified more than 500 000 druglike compounds using this system in the past 3 years. We report various components of this high-throughput purification system and some of our purification results. 相似文献
78.
Dramatic Influence of an Anionic Donor on the Oxygen‐Atom Transfer Reactivity of a MnV–Oxo Complex 下载免费PDF全文
Heather M. Neu Dr. Matthew G. Quesne Tzuhsiung Yang Dr. Katharine A. Prokop‐Prigge Prof. Kyle M. Lancaster James Donohoe Prof. Serena DeBeer Dr. Sam P. de Visser Prof. David P. Goldberg 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(45):14584-14588
Addition of an anionic donor to an MnV(O) porphyrinoid complex causes a dramatic increase in 2‐electron oxygen‐atom‐transfer (OAT) chemistry. The 6‐coordinate [MnV(O)(TBP8Cz)(CN)]? was generated from addition of Bu4N+CN? to the 5‐coordinate MnV(O) precursor. The cyanide‐ligated complex was characterized for the first time by Mn K‐edge X‐ray absorption spectroscopy (XAS) and gives Mn?O=1.53 Å, Mn?CN=2.21 Å. In combination with computational studies these distances were shown to correlate with a singlet ground state. Reaction of the CN? complex with thioethers results in OAT to give the corresponding sulfoxide and a 2e?‐reduced MnIII(CN)? complex. Kinetic measurements reveal a dramatic rate enhancement for OAT of approximately 24 000‐fold versus the same reaction for the parent 5‐coordinate complex. An Eyring analysis gives ΔH≠=14 kcal mol?1, ΔS≠=?10 cal mol?1 K?1. Computational studies fully support the structures, spin states, and relative reactivity of the 5‐ and 6‐coordinate MnV(O) complexes. 相似文献
79.
Apeng Chen Kyle B. Lynch Xiaochun Wang Joann J. Lu Congying Gu Shaorong Liu 《Analytica chimica acta》2014
We integrate a high-pressure electroosmotic pump (EOP), a nanoflow gradient generator, and a capillary column into a miniaturized liquid chromatographic system that can be directly coupled with a mass spectrometer for proteomic analysis. We have recently developed a low-cost high-pressure EOP capable of generating pressure of tens of thousands psi, ideal for uses in miniaturized HPLC. The pump worked smoothly when it was used for isocratic elutions. When it was used for gradient elutions, generating reproducible gradient profiles was challenging; because the pump rate fluctuated when the pump was used to pump high-content organic solvents. This presents an issue for separating proteins/peptides since high-content organic solvents are often utilized. In this work, we solve this problem by incorporating our high-pressure EOP with a nano-flow gradient generator so that the EOP needs only to pump an aqueous solution. With this combination, we develop a capillary-based nano-HPLC system capable of performing nano-flow gradient elution; the pump rate is stable, and the gradient profiles are reproducible and can be conveniently tuned. To demonstrate its utility, we couple it with either a UV absorbance detector or a mass spectrometer for peptide separations. 相似文献
80.
Combinatorially Designed Lipid‐like Nanoparticles for Intracellular Delivery of Cytotoxic Protein for Cancer Therapy 下载免费PDF全文
Dr. Ming Wang Kyle Alberti Shuo Sun Carlos Luis Arellano Prof. Dr. Qiaobing Xu 《Angewandte Chemie (International ed. in English)》2014,53(11):2893-2898
An efficient and safe method to deliver active proteins into the cytosol of targeted cells is highly desirable to advance protein‐based therapeutics. A novel protein delivery platform has been created by combinatorial design of cationic lipid‐like materials (termed “lipidoids”), coupled with a reversible chemical protein engineering approach. Using ribonuclease A (RNase A) and saporin as two representative cytotoxic proteins, the combinatorial lipidoids efficiently deliver proteins into cancer cells and inhibit cell proliferation. A study of the structure–function relationship reveals that the electrostatic and hydrophobic interactions between the lipidoids and the protein play a vital role in the formation of protein–lipidoid nanocomplexes and intracellular delivery. A representative lipidoid (EC16‐1) protein nanoparticle formulation inhibits cell proliferation in vitro and suppresses tumor growth in a murine breast cancer model. 相似文献