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Implementation of a pharmocokinetic approach to a baculovirus system for analytic solutions to virus and cell interactions

机译:用于对病毒和细胞相互作用分析溶液的杆状病毒系统的药状途径

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A quantitative investigation was undertaken to study the overall effects of the individual stages of the trafficking of a baculovirus system (AcMNPV) into the nucleus of a cell. The limiting rate constants, k{sub}r and k{sub}λ, showed thebehavior can dramatically change based upon these rate constants. This pharmocokinetic modeling was useful in predicting the overall virus concentrations in each stage of the virus and cell interactions. This model can be used further to predict othertypes of virus systems in order to increase the ability of predicting protein production in many processes including viral gene therapy.
机译:进行了定量调查,以研究将杆菌病毒系统(ACMNPV)贩运贩运的个体阶段的整体效应研究到细胞核中。限制率常数,k {sub} r和k {sub}λ,显示出基于这些速率常数的最大化可以显着地改变。该药效性建模可用于预测病毒和细胞相互作用的每个阶段的整体病毒浓度。该模型可以进一步用于预测病毒系统的其他类型,以提高预测蛋白质产生的能力,包括病毒基因治疗。

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