论文标题
在RNA-蛋白质动力学的相位场模型上
On a phase field model for RNA-Protein dynamics
论文作者
论文摘要
分析了描述蛋白-RNA复合物形成的相位场模型。考虑一种单一蛋白质,两种RNA种和两个复合物。蛋白质和RNA物种受耦合反应扩散方程的控制,这也取决于两个复合物。后者是由两个Cahn-Hilliard方程驱动的,其潜力和反应项取决于溶液变量。所得的非线性耦合系统配备了无升华边界条件和合适的初始条件。前者需要一些质量保护约束,这也是由于反应术语的性质。建立了一个有界(二维或三维域)中全球弱解决方案的存在。在二维中,显示了一些加权定期性能。特别是,复合物瞬间与纯相均匀分离。利用这一结果,证明了独特的延续属性。在许多技术困难中,最重要的是,这两个复合物最初是不存在的事实,因此它们的初始条件为零,即它们从纯阶段开始。因此,我们必须特别求解一个具有两个耦合的Cahn-Hilliard方程的系统,该系统具有单数势和非线性源,而无需在初始基准上通常假设,即初始阶段不能纯净。这种新颖性需要一种新的方法来估算合适的$ l^p(l^2)$ - 带有$ p \ in(1,2)$的空间中的化学潜力。该技术可以扩展到其他型号,例如,众所周知的Cahn-Hilliard-oon方程。
A phase field model which describes the formation of protein-RNA complexes subject to phase segregation is analyzed. A single protein, two RNA species, and two complexes are considered. Protein and RNA species are governed by coupled reaction-diffusion equations which also depend on the two complexes. The latter ones are driven by two Cahn-Hilliard equations with Flory-Huggins potential and reaction terms depending on the solution variables. The resulting nonlinear coupled system is equipped with no-flux boundary conditions and suitable initial conditions. The former ones entail some mass conservation constraints which are also due to the nature of the reaction terms. The existence of global weak solutions in a bounded (two- or) three-dimensional domain is established. In dimension two, some weighted-in-time regularity properties are shown. In particular, the complexes instantaneously get uniformly separated from the pure phases. Taking advantage of this result, a unique continuation property is proven. Among the many technical difficulties, the most significant one arises from the fact that the two complexes are initially nonexistent, so their initial conditions are zero i.e., they start from a pure phase. Thus we must solve, in particular, a system of two coupled Cahn-Hilliard equations with singular potential and nonlinear sources without the usual assumption on the initial datum, i.e., the initial phase cannot be pure. This novelty requires a new approach to estimate the chemical potential in a suitable $L^p(L^2)$-space with $p\in(1,2)$. This technique can be extended to other models like, for instance, the well-known Cahn-Hilliard-Oono equation.