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超螺旋和环形 DNA 半浓混合体中意想不到的缠结动力学。

Unexpected entanglement dynamics in semidilute blends of supercoiled and ring DNA.

机构信息

Department of Physics and Biophysics, University of San Diego, 5998 Alcala Park, San Diego, CA 92110, USA.

Department of Materials Science and Engineering, Beckman Institute for Advanced Science and Technology & Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

Soft Matter. 2020 Jan 7;16(1):152-161. doi: 10.1039/c9sm01767d. Epub 2019 Nov 27.

Abstract

Blends of polymers of different topologies, such as ring and supercoiled, naturally occur in biology and often exhibit emergent viscoelastic properties coveted in industry. However, due to their complexity, along with the difficulty of producing polymers of different topologies, the dynamics of topological polymer blends remains poorly understood. We address this void by using both passive and active microrheology to characterize the linear and nonlinear rheological properties of blends of relaxed circular and supercoiled DNA. We characterize the dynamics as we vary the concentration from below the overlap concentration c* to above (0.5c* to 2c*). Surprisingly, despite working at the dilute-semidilute crossover, entanglement dynamics, such as elastic plateaus and multiple relaxation modes, emerge. Finally, blends exhibit an unexpected sustained elastic response to nonlinear strains not previously observed even in well-entangled linear polymer solutions.

摘要

不同拓扑聚合物的混合物,如环状和超螺旋,在生物学中自然存在,并且通常表现出在工业中受到青睐的新的粘弹性特性。然而,由于其复杂性,以及生产不同拓扑聚合物的困难,拓扑聚合物混合物的动力学仍然了解甚少。我们通过使用被动和主动微流变学来表征松弛的圆形和超螺旋 DNA 混合物的线性和非线性流变性质来解决这一空白。我们在浓度从低于重叠浓度 c变化到高于(0.5c至 2c*)时对动力学进行了表征。令人惊讶的是,尽管在稀-半稀过渡区工作,但出现了缠结动力学,如弹性平台和多种松弛模式。最后,混合物表现出对非线性应变的意外持续弹性响应,即使在以前甚至在良好缠结的线性聚合物溶液中也没有观察到这种响应。

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