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Browsing by Subject "Solubility"

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    Multielectron Organic Redoxmers for Energy-Dense Redox Flow Batteries
    (ACS, 2022-01) Fang, Xiaoting; Li, Zhiguang; Zhao, Yuyue; Yue, Diqing; Zhang, Lu; Wei, Xiaoliang; Mechanical Engineering, School of Engineering and Technology
    Redox flow battery is a highly promising stationary energy storage method, but the limited energy density and high chemical cost are among the main barriers for commercialization. Multielectron organic redoxmers represent a family of structurally tailorable candidates that can achieve multiplied energy density with decreased materials consumption, potentially resulting in a viable solution to address these challenges. Here, the recent development of organic molecules with reversible multiredox activities in both aqueous and nonaqueous electrolytes is reviewed. The major focus is on the fundamental correlation between the chemical structures and the functional properties of reported multielectron organic molecules. Valuable insights are offered on rational structural design strategies for improving the relevant physicochemical and electrochemical properties. Finally, the current challenges are discussed to suggest future research needs along the avenue of using the multielectron approach to achieve energy-dense, stable, cost-effective redox flow batteries.
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    Titer estimation for quality control (TEQC) method: A practical approach for optimal production of protein complexes using the baculovirus expression vector system
    (Public Library of Science, 2018-04-03) Imasaki, Tsuyoshi; Wenzel, Sabine; Yamada, Kentaro; Bryant, Megan L.; Takagi, Yuichiro; Biochemistry and Molecular Biology, School of Medicine
    The baculovirus expression vector system (BEVS) is becoming the method of choice for expression of many eukaryotic proteins and protein complexes for biochemical, structural and pharmaceutical studies. Significant technological advancement has made generation of recombinant baculoviruses easy, efficient and user-friendly. However, there is a tremendous variability in the amount of proteins made using the BEVS, including different batches of virus made to express the same proteins. Yet, what influences the overall production of proteins or protein complexes remains largely unclear. Many downstream applications, particularly protein structure determination, require purification of large quantities of proteins in a repetitive manner, calling for a reliable experimental set-up to obtain proteins or protein complexes of interest consistently. During our investigation of optimizing the expression of the Mediator Head module, we discovered that the 'initial infectivity' was an excellent indicator of overall production of protein complexes. Further, we show that this initial infectivity can be mathematically described as a function of multiplicity of infection (MOI), correlating recombinant protein yield and virus titer. All these findings led us to develop the Titer Estimation for Quality Control (TEQC) method, which enables researchers to estimate initial infectivity, titer/MOI values in a simple and affordable way, and to use these values to quantitatively optimize protein expressions utilizing BEVS in a highly reproducible fashion.
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