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arXiv 1601.01425cond-mat.stat-mech
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空间非均匀聚合物的高斯涨落

Gaussian fluctuations of spatially inhomogeneous polymers

Yohai Bar-Sinai, Eran Bouchbinder

摘要:

非均相聚合物在自然界和生物技术应用中的各种细胞过程中发挥着重要作用。在有限温度下,非均匀聚合物表现出非平凡的热波动。在更广泛的背景下,这些是空间非均匀系统中波动的相对简单的例子,与均匀系统相比,它们的理解较少。我们开发了一个统计理论的扭转,拉伸和弯曲高斯波动的不均匀聚合物,其中的不均匀性是一个包含变量的大小和机械性能,使用连续和离散的方法。首先,我们在连续场论中解析地计算了非均匀聚合物的完整本征值和本征模谱。特别地,我们证明了包含体内外的波数在本征值指数中几乎是线性的,并且具有非平凡系数。其次,我们解决了相应的离散问题,并强调连续谱和离散谱之间的根本区别。特别是,我们表明,在一定的波数以上的离散谱的变化定性和离散倏逝本征模,没有连续对应,出现。这些差异的统计热力学意义,然后探讨通过计算波动引起的力量与自由能的变化与夹杂物的性质(例如~通过吸附分子形成的不均匀性)或具有外部几何约束。前者,这是波动引起的贡献吸附分子的结合力,被证明是由短波长的影响,因此不能使用连续的方法计算。后者,另一方面,被证明是占主导地位的长波长形状的波动,因此是适当的连续理论描述。

英文摘要:

Inhomogeneous polymers play an important role in various cellular processes, both in nature and in biotechnological applications. At finite temperatures, inhomogeneous polymers exhibit non-trivial thermal fluctuations. In a broader context, these are relatively simple examples for fluctuations in spatially inhomogeneous systems, which are less understood compared to their homogeneous counterparts. We develop a statistical theory of torsional, extensional and bending Gaussian fluctuations of inhomogeneous polymers, where the inhomogeneity is an inclusion of variable size and mechanical properties, using both continuum and discrete approaches. First, we analytically calculate the complete eigenvalue and eigenmode spectrum of the inhomogeneous polymer within a continuum field theory. In particular, we show that the wavenumber inside and outside of the inclusion is nearly linear in the eigenvalue index, with a nontrivial coefficient. Second, we solve the corresponding discrete problem, and highlight fundamental differences between the continuum and discrete spectra. In particular, we demonstrate that above a certain wavenumber the discrete spectrum changes qualitatively and discrete evanescent eigenmodes, that do not have continuum counterparts, emerge. The statistical thermodynamic implications of these differences are then explored by calculating fluctuation-induced forces associated with free-energy variations with either the inclusion properties (e.g.~inhomogeneity formed by adsorbing molecules) or with an external geometric constraint. The former, which is the fluctuation-induced contribution to the adsorbing molecules binding force, is shown to be affected by short wavelengths and thus cannot be calculated using the continuum approach. The latter, on the other hand, is shown to be dominated by long wavelength shape fluctuations and hence is properly described by the continuum theory.

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