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利用平流整体流动来控制 Min 蛋白模式。

Directing Min protein patterns with advective bulk flow.

机构信息

Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, the Netherlands.

Arnold Sommerfeld Center for Theoretical Physics and Center for NanoScience, Department of Physics, Ludwig-Maximilians-Universität München, Munich, Germany.

出版信息

Nat Commun. 2023 Jan 27;14(1):450. doi: 10.1038/s41467-023-35997-0.

Abstract

The Min proteins constitute the best-studied model system for pattern formation in cell biology. We theoretically predict and experimentally show that the propagation direction of in vitro Min protein patterns can be controlled by a hydrodynamic flow of the bulk solution. We find downstream propagation of Min wave patterns for low MinE:MinD concentration ratios, upstream propagation for large ratios, but multistability of both propagation directions in between. Whereas downstream propagation can be described by a minimal model that disregards MinE conformational switching, upstream propagation can be reproduced by a reduced switch model, where increased MinD bulk concentrations on the upstream side promote protein attachment. Our study demonstrates that a differential flow, where bulk flow advects protein concentrations in the bulk, but not on the surface, can control surface-pattern propagation. This suggests that flow can be used to probe molecular features and to constrain mathematical models for pattern-forming systems.

摘要

Min 蛋白构成了细胞生物学中模式形成的研究得最好的模型体系。我们从理论上预测并通过实验证明,体外 Min 蛋白模式的传播方向可以通过本体溶液的流体力学流来控制。我们发现,对于低 MinE:MinD 浓度比,Min 波模式的下游传播;对于大的浓度比,上游传播;但是在两者之间存在两种传播方向的多稳定性。虽然下游传播可以用一个忽略 MinE 构象转换的最小模型来描述,但是上游传播可以用一个简化的开关模型来重现,其中上游侧增加的 MinD 本体浓度促进了蛋白质的附着。我们的研究表明,差异流可以控制表面模式的传播,其中本体流在本体中输运蛋白质浓度,但不在表面上。这表明可以利用流动来探测分子特征,并约束模式形成系统的数学模型。

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