Robles-Hernández Beatriz, Malo de Molina Paula, Asenjo-Sanz Isabel, Gonzalez-Burgos Marina, Pasini Stefano, Pomposo José A, Arbe Arantxa, Colmenero Juan
Donostia International Physics Center (DIPC), 20018 Donostia-San Sebastián, Spain.
Centro de Física de Materiales/Materials Physics Center (CFM/MPC), 20018 Donostia-San Sebastián, Spain.
Macromolecules. 2024 May 7;57(10):4706-4716. doi: 10.1021/acs.macromol.4c00182. eCollection 2024 May 28.
We present a neutron spin echo (NSE) investigation to examine the impact of macromolecular crowding on the dynamics of single-chain nanoparticles (SCNPs), serving as synthetic models for biomacromolecules with flexibility and internal degrees of freedom, such as intrinsically disordered proteins (IDPs). In particular, we studied the dynamics of a medium-size poly(methyl methacrylate) (PMMA)-based SCNP (33 kDa) in solutions with low- (10 kDa) and high- (100 kDa) molecular weight analogous deuterated PMMA linear crowders. The dynamic structure factors of the SCNPs in dilute solution show certain degrees of freedom, yet the analysis in terms of the Zimm model reveals high internal friction that effectively stiffens the chain-a phenomenon also observed for IDPs. Under crowding conditions, the internal dynamics remains essentially unchanged, but the center-of-mass diffusion slows down. The effective viscosity felt by the SCNPs at the timescales probed by NSE is lower than the macroscopic viscosity of the crowder solution, and it does not depend significantly on the molecular weight.
我们进行了一项中子自旋回波(NSE)研究,以考察大分子拥挤对单链纳米颗粒(SCNP)动力学的影响,这些单链纳米颗粒作为具有灵活性和内部自由度的生物大分子的合成模型,例如内在无序蛋白(IDP)。具体而言,我们研究了一种中等尺寸的基于聚甲基丙烯酸甲酯(PMMA)的SCNP(33 kDa)在含有低分子量(10 kDa)和高分子量(100 kDa)类似氘代PMMA线性拥挤剂的溶液中的动力学。稀溶液中SCNP的动态结构因子显示出一定程度的自由度,但根据齐姆模型进行的分析揭示了较高的内摩擦,这有效地使链变硬——这种现象在IDP中也有观察到。在拥挤条件下,内部动力学基本保持不变,但质心扩散减慢。在NSE探测的时间尺度上,SCNP感受到的有效粘度低于拥挤剂溶液的宏观粘度,并且它对分子量的依赖性不显著。