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肽凝胶动力学的单分子研究揭示了预应力状态。

Single-Molecule Study of Peptide Gel Dynamics Reveals States of Prestress.

作者信息

Cox Henry, Xu Hai, Waigh Thomas A, Lu Jian R

机构信息

Biological Physics, School of Physics and Astronomy , University of Manchester , Manchester M13 9PL , U.K.

Centre for Bioengineering and Biotechnology , China University of Petroleum (East China) , 66 Changjiang West Road , Qingdao 266555 , China.

出版信息

Langmuir. 2018 Dec 4;34(48):14678-14689. doi: 10.1021/acs.langmuir.8b03334. Epub 2018 Nov 21.

Abstract

De novo peptide surfactant (IK) gels provide an ideal system to study the complex dynamics of lightly cross-linked semiflexible fibers because of their large contour lengths, simple chemistry, and slow dynamics. We used single-molecule fluorescence microscopy to record individual fibers and Fourier decomposition of the fiber dynamics to separate thermal contributions to the persistence length from compressive states of prestress (SPS). Our results show that SPS in the network depend strongly on peptide concentration, buffer, and pH and that the fibril energies in SPS follow a Lévy distribution. The presence of SPS in the network imply that collective states of self-stress are also present. Therefore, semiflexible polymer gels need to be considered as complex load-bearing structures and the mean field models for polymer gel elasticity and dynamics often applied to them will not be fully representative of the behavior at the nanoscale. We quantify the impact of cross-links on reptation tube dynamics, which provides a second population of tube fluctuations in addition to those expected for uncross-linked entangled solutions.

摘要

从头合成肽表面活性剂(IK)凝胶由于其较大的轮廓长度、简单的化学性质和缓慢的动力学,为研究轻度交联的半柔性纤维的复杂动力学提供了一个理想的体系。我们使用单分子荧光显微镜记录单个纤维,并对纤维动力学进行傅里叶分解,以将热对持久长度的贡献与预应力压缩状态(SPS)区分开来。我们的结果表明,网络中的SPS强烈依赖于肽浓度、缓冲液和pH值,并且SPS中的原纤维能量遵循Lévy分布。网络中SPS的存在意味着自应力的集体状态也存在。因此,半柔性聚合物凝胶需要被视为复杂的承载结构,而通常应用于它们的聚合物凝胶弹性和动力学的平均场模型将不能完全代表纳米尺度下的行为。我们量化了交联对爬行管动力学的影响,这除了未交联缠结溶液预期的那些波动外,还提供了第二批管波动。

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