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手性大分子环形聚集体的几何模板。

A geometrical template for toroidal aggregates of chiral macromolecules.

作者信息

Charvolin J, Sadoc J-F

机构信息

Laboratoire de Physique des Solides, Université Paris-Sud et CNRS, UMR 8502, F-91405 Orsay, France.

出版信息

Eur Phys J E Soft Matter. 2008 Mar;25(3):335-41. doi: 10.1140/epje/i2008-10313-8. Epub 2008 Apr 9.

Abstract

The formation of toroidal aggregates by long chiral molecules of biological origin, as collagen, f-actin and DNA, or by chiral synthetic polypeptides has been observed in specific ionic environments. Such aggregates have received considerable attention in order to identify the various physical factors susceptible to contribute to this original morphogenesis, particularly in the case of those formed by DNA. We consider here the eventual role of a spontaneous uniform twist of micrometric pitch whose possible occurrence is suggested by some observations and by recent studies of DNA dense phases exhibiting cholesteric and "blue" phase structures. Following an approach inspired by the geometry and topology of fiber bundles, we show that the necessity to propagate such a twist in a dense bundle of fibers leads to the formation of aggregates having a toroidal shape and, in the case of the nanometric aggregates of DNA, characteristic sizes similar to those observed.

摘要

在特定离子环境中,已观察到生物源长手性分子(如胶原蛋白、f - 肌动蛋白和DNA)或手性合成多肽形成环形聚集体。为了确定可能促成这种原始形态发生的各种物理因素,此类聚集体受到了相当多的关注,特别是在DNA形成的聚集体的情况下。我们在此考虑微米级螺距的自发均匀扭曲的最终作用,一些观察结果以及最近对呈现胆甾相和“蓝色”相结构的DNA致密相的研究表明了这种扭曲可能存在。遵循受纤维束几何形状和拓扑结构启发的方法,我们表明在密集的纤维束中传播这种扭曲的必要性会导致形成环形聚集体,并且在DNA的纳米聚集体的情况下,其特征尺寸与观察到的尺寸相似。

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