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通过开环聚合诱导自组装(ROPISA)制备聚(L-脯氨酸)稳定的多肽纳米结构。

Poly(l-proline)-Stabilized Polypeptide Nanostructures via Ring-Opening Polymerization-Induced Self-Assembly (ROPISA).

机构信息

Department of Chemistry, RCSI University of Medicine and Health Sciences, 123 St. Stephen's Green, D02 YN77 Dublin, Ireland.

Aston Institute for Membrane Excellence, Aston University, B4 7ET Birmingham, U.K.

出版信息

ACS Macro Lett. 2024 Aug 20;13(8):1031-1036. doi: 10.1021/acsmacrolett.4c00400. Epub 2024 Jul 29.

Abstract

Poly(proline) II helical motifs located at the protein-water interface stabilize the three-dimensional structures of natural proteins. Reported here is the first example of synthetic biomimetic poly(proline)-stabilized polypeptide nanostructures obtained by a straightforward ring-opening polymerization-induced self-assembly (ROPISA) process through consecutive -carboxyanhydride (NCA) polymerization. It was found that the use of multifunctional 8-arm initiators is critical for the formation of nanoparticles. Worm-like micelles as well as spherical morphologies were obtained as confirmed by dynamic light scattering (DLS), transmission electron microscopy (TEM), and small angle X-ray scattering (SAXS). The loading of the nanostructures with dyes is demonstrated. This fast and open-vessel procedure gives access to amino acids-based nanomaterials with potential for applications in nanomedicine.

摘要

位于蛋白质-水界面的多(脯氨酸) II 螺旋基序稳定了天然蛋白质的三维结构。本文报道了首例通过开环聚合诱导自组装(ROPISA)过程,通过连续的 - 羧酸酐(NCA)聚合获得的合成仿生聚(脯氨酸)稳定的多肽纳米结构。研究发现,使用多功能 8 臂引发剂对于纳米粒子的形成至关重要。通过动态光散射(DLS)、透射电子显微镜(TEM)和小角 X 射线散射(SAXS)证实了蠕虫状胶束和球形形态的形成。还证明了纳米结构的染料加载。这种快速、开放容器的方法可以获得基于氨基酸的纳米材料,这些材料在纳米医学中有应用的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59bb/11340022/393378351498/mz4c00400_0001.jpg

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