Suppr超能文献

由诸如弹性蛋白样重组蛋白等内在无序蛋白质聚合物组成的自组装系统。

Self-assembling systems comprising intrinsically disordered protein polymers like elastin-like recombinamers.

作者信息

Juanes-Gusano Diana, Santos Mercedes, Reboto Virginia, Alonso Matilde, Rodríguez-Cabello José Carlos

机构信息

BIOFORGE (Group for Advanced Materials and Nanobiotechnology) CIBER-BBN, Edificio Lucía, University of Valladolid, Valladolid, Spain.

出版信息

J Pept Sci. 2022 Jan;28(1):e3362. doi: 10.1002/psc.3362. Epub 2021 Sep 20.

Abstract

Despite lacking cooperatively folded structures under native conditions, numerous intrinsically disordered proteins (IDPs) nevertheless have great functional importance. These IDPs are hybrids containing both ordered and intrinsically disordered protein regions (IDPRs), the structure of which is highly flexible in this unfolded state. The conformational flexibility of these disordered systems favors transitions between disordered and ordered states triggered by intrinsic and extrinsic factors, folding into different dynamic molecular assemblies to enable proper protein functions. Indeed, prokaryotic enzymes present less disorder than eukaryotic enzymes, thus showing that this disorder is related to functional and structural complexity. Protein-based polymers that mimic these IDPs include the so-called elastin-like polypeptides (ELPs), which are inspired by the composition of natural elastin. Elastin-like recombinamers (ELRs) are ELPs produced using recombinant techniques and which can therefore be tailored for a specific application. One of the most widely used and studied characteristic structures in this field is the pentapeptide (VPGXG) . The structural disorder in ELRs probably arises due to the high content of proline and glycine in the ELR backbone, because both these amino acids help to keep the polypeptide structure of elastomers disordered and hydrated. Moreover, the recombinant nature of these systems means that different sequences can be designed, including bioactive domains, to obtain specific structures for each application. Some of these structures, along with their applications as IDPs that self-assemble into functional vesicles or micelles from diblock copolymer ELRs, will be studied in the following sections. The incorporation of additional order- and disorder-promoting peptide/protein domains, such as α-helical coils or β-strands, in the ELR sequence, and their influence on self-assembly, will also be reviewed. In addition, chemically cross-linked systems with controllable order-disorder balance, and their role in biomineralization, will be discussed. Finally, we will review different multivalent IDPs-based coatings and films for different biomedical applications, such as spatially controlled cell adhesion, osseointegration, or biomaterial-associated infection (BAI).

摘要

尽管在天然条件下缺乏协同折叠结构,但许多内在无序蛋白(IDP)仍具有重要的功能。这些IDP是包含有序和内在无序蛋白区域(IDPR)的杂合体,其结构在这种未折叠状态下具有高度灵活性。这些无序系统的构象灵活性有利于由内在和外在因素触发的无序和有序状态之间的转变,折叠成不同的动态分子组装体以实现适当的蛋白质功能。事实上,原核酶比真核酶的无序程度低,因此表明这种无序与功能和结构复杂性有关。模拟这些IDP的基于蛋白质的聚合物包括所谓的弹性蛋白样多肽(ELP),其灵感来自天然弹性蛋白的组成。弹性蛋白样重组体(ELR)是使用重组技术生产的ELP,因此可以针对特定应用进行定制。该领域最广泛使用和研究的特征结构之一是五肽(VPGXG)。ELR中的结构无序可能是由于ELR主链中脯氨酸和甘氨酸的含量高,因为这两种氨基酸都有助于保持弹性体的多肽结构无序和水合。此外,这些系统的重组性质意味着可以设计不同的序列,包括生物活性结构域,以获得适合每种应用的特定结构。以下部分将研究其中一些结构,以及它们作为IDP从双嵌段共聚物ELR自组装成功能性囊泡或胶束的应用。还将综述在ELR序列中加入额外的促进有序和无序的肽/蛋白质结构域,如α-螺旋卷曲或β-链,以及它们对自组装的影响。此外,还将讨论具有可控有序-无序平衡的化学交联系统及其在生物矿化中的作用。最后,我们将综述用于不同生物医学应用的不同多价基于IDP的涂层和薄膜,如空间控制的细胞粘附、骨整合或生物材料相关感染(BAI)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验