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Mathematical modeling of HIV-like particle assembly in vitro.
- Source :
-
Mathematical Biosciences . Jun2017, Vol. 288, p46-51. 6p. - Publication Year :
- 2017
-
Abstract
- In vitro , the recombinant HIV-1 Gag protein can generate spherical particles with a diameter of 25–30 nm in a fully defined system. It has approximately 80 building blocks, and its intermediates for assembly are abundant in geometry. Accordingly, there are a large number of nonlinear equations in the classical model. Therefore, it is difficult to compute values of geometry parameters for intermediates and make the mathematical analysis using the model. In this work, we develop a new model of HIV-like particle assembly in vitro by using six-fold symmetry of HIV-like particle assembly to decrease the number of geometry parameters. This method will greatly reduce computational costs and facilitate the application of the model. Then, we prove the existence and uniqueness of the positive equilibrium solution for this model with 79 nonlinear equations. Based on this model, we derive the interesting result that concentrations of all intermediates at equilibrium are independent of three important parameters, including two microscopic on-rate constants and the size of nucleating structure. Before equilibrium, these three parameters influence the concentration variation rates of all intermediates. We also analyze the relationship between the initial concentration of building blocks and concentrations of all intermediates. Furthermore, the bounds of concentrations of free building blocks and HIV-like particles are estimated. These results will be helpful to guide HIV-like particle assembly experiments and improve our understanding of the assembly dynamics of HIV-like particles in vitro . [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00255564
- Volume :
- 288
- Database :
- Academic Search Index
- Journal :
- Mathematical Biosciences
- Publication Type :
- Periodical
- Accession number :
- 122648358
- Full Text :
- https://doi.org/10.1016/j.mbs.2017.02.010