Expression Construct Design

Expression vectors are engineered so that any cloned insert can be transcribed into RNA, and, in many instances, even translated into protein. cDNA expression libraries can be constructed in specially designed vectors derived from either plasmids or bacteriophage A. Proteins encoded by the various cDNA clones within such expression libraries can be synthesized in the host cells, and if suitable assays are available to identify a particular protein, its corresponding cDNA clone can be identified and isolated. Expression vectors designed for RNA expression or protein expression, or both, are available. 

Lyons, R.E., Lesieur, E., Kim, M., Wong, D., Brownlee, A., Pearson, R., and Elvin, C., The development of synthetic genes encoding repetitive resilin-like polypeptides Construct design, bacterial expression and rapid purification. Protein Eng. Design Select., 20(1), 25-32, 2007. 

Expression constructs were designed with the receptor sequence cloned into a pFastBac vector. A schematic of the receptor construct in the vector is shown in Fig. 2A. This construct utilizes a GP64 or poM promoter to drive receptor expression, an HA signal sequence to enhance localization in the Sf9 ceU membrane and a C-terminal Prescission protease (PP) cleavage site followed by FLAG and His tags which permit detection and purification, respectively. Restriction sites before and after the receptor sequence facilitate transfer of sequences between plasmids with different promoters, signal... 

Structure-based drug design (SBDD) can provide valuable guidance to drug discovery programs. Robust construct design and expression, protein... 

Note that subtracting an amount log a from the coordinate values along the abscissa is equivalent to dividing each of the t s by the appropriate a-p value. This means that times are represented by the reduced variable t/a in which t is expressed as a multiple or fraction of a-p which is called the shift factor. The temperature at which the master curve is constructed is an arbitrary choice, although the glass transition temperature is widely used. When some value other than Tg is used as a reference temperature, we shall designate it by the symbol To. 

This paper explores how models may be developed to account for the relationship between the stable isotope composition of a body tissue of an organism and its diet. The main approach taken is to express this relationship as an explicit equation, or a DIFF , and then to show how the values of such a DIFF can be evaluated from published experimental data. These values can be expected to have a much wider meaning than a simple encapsulation of a particular experimental design. As a main example, we show how the values may be used to constract a metabolic model in which the synthesis of non-essential amino acid for collagen construction can be treated. A second example is to show how the evaluation, in terms of diet, of the spacing between collagen and carbonate 6 C may be put on a rigorous basis. 

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