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最小超分子聚合物模型中的自发结构转变和晶体形成。

Spontaneous structural transition and crystal formation in minimal supramolecular polymer model.

机构信息

Department of Molecular Microbiology and Biotechnology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997801, Israel.

Biophysics and Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA.

出版信息

Sci Adv. 2016 Feb 12;2(2):e1500827. doi: 10.1126/sciadv.1500827. eCollection 2016 Feb.

Abstract

The association of building blocks into supramolecular polymers allows the fabrication of diverse functional architectures at the nanoscale. The use of minimal assembly units to explore polymer dynamics and phase transitions significantly contributes to the application of polymer physicochemical paradigms in the field of supramolecular polymers. We present a minimal model that displays spontaneous coordinated structural transitions between micro- and nanostructures, hydrogels with nanoscale order, and single crystals. The simple amphiphilic 9-fluorenylmethoxycarbonyl-3,4-dihydroxyphenylalanine (Fmoc-DOPA) modified amino acid undergoes a noninduced transition from spherical assemblies into nanofibrils followed by sol-gel transition, nanotube formation via intermediate assembly, and crystallization within the gel. Notably, the transition kinetics is slow enough to allow both multistage and multiscale characterization of the supramolecular arrangement using electron microscopy, vibrational and circular dichroism spectroscopies, nuclear magnetic resonance, and x-ray crystallography. This minimalistic system is the first comprehensive model for a complete spontaneous structural transition between diverse states governed by distinct molecular interactions.

摘要

砌块组装成超分子聚合物,可在纳米尺度上构建多样化的功能结构。采用最小的组装单元来探索聚合物动力学和相转变,这对将聚合物物理化学范式应用于超分子聚合物领域有重要意义。我们提出了一个简单模型,该模型显示了微观和纳米结构、具有纳米级有序的水凝胶和单晶之间自发协调结构转变。简单的两亲性 9-芴甲氧羰基-3,4-二羟基苯丙氨酸(Fmoc-DOPA)修饰氨基酸经历非诱导从球形组装体到纳米纤维的转变,然后是溶胶-凝胶转变、通过中间组装形成纳米管以及凝胶内结晶。值得注意的是,该转变动力学足够慢,可使用电子显微镜、振动和圆二色光谱、核磁共振和 X 射线晶体学对超分子排列进行多阶段和多尺度的表征。这个极简系统是第一个全面的模型,可实现由不同分子相互作用控制的不同状态之间的完整自发结构转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dca/4758747/dd24243b2fb7/1500827-F1.jpg

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