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用于二氧化硅沉淀的肽:指导矿化的氨基酸序列

Peptides for Silica Precipitation: Amino Acid Sequences for Directing Mineralization.

作者信息

Ozaki Makoto, Sakashita Shungo, Hamada Yoshio, Usui Kenji

机构信息

FIRST (Faculty of Frontiers of Innovative Research in Science and Technology), Konan University, 650-0047 Kobe, Japan.

出版信息

Protein Pept Lett. 2018;25(1):15-24. doi: 10.2174/0929866525666171214111007.

Abstract

BACKGROUND

Peptides are promising compounds for use in inorganic or organic-inorganic hybrid syntheses (mineralization) and offer several advantages over proteins. Meanwhile, silica-based nanomaterials have been extensively investigated for many years because of their potential application in a diverse range of technologies, including catalysis, sensing, separation, enzyme immobilization, and gene and drug delivery. Considerable progress has been made over the past decade in understanding the molecular mechanisms underpinning biosilicification and the biomimetic synthesis of patterned nanosilica using peptides.

OBJECTIVES

This mini-review focuses on various peptide sequences, especially short peptide sequences (30 residues or less), for silica mineralization.

METHODS

We first briefly review early studies on silica mineralization using proteins to provide background information. This is followed by a discussion of promising peptide sequences and attempts to discern the relationship between amino acid sequence, their potential for mineralization, and the properties of the mineral product.

RESULTS

The synthetic control of silica mineralization using engineered proteins, such as recombinant silicateins and silaffins, was inspired by silica biomineralization by natural proteins from organisms (sponges, diatoms, and plants). Concurrently, several papers described the utility of well-structured protein assemblies as templates for silica mineralization. These template-directed syntheses of well-structured silica deposits were first conducted using natural proteins or protein assemblies such as collagen fibers and virus hollow protein tubes. Then we reviewed a selection of short peptides (30 residues or less) that had been successfully used for silica mineralization. Almost all peptides developed to date can be sorted by classification like proteins (synthetic control of silica mineralization or utility of templates for silica mineralization): the first class of peptides is used for peptide-directed synthesis, and the second is used for template-directed synthesis after the peptides have assembled and formed nanostructure such as fibers and tubes. The presented peptides were classified and arranged according to the classification. Additionally, we briefly introduced silica mineralization triggered by the combination of short silica-precipitating peptides and template molecules.

CONCLUSION

In this mini-review we focused on various peptide sequences, especially short peptide sequences of 30 residues or less, designed for silica mineralization. The peptides have been used both for peptide-directed silica mineralization and for template-directed silica mineralization. The recent advances in peptide-driven mineralization reviewed here suggest that it will soon be possible to completely control the silica mineralization process using peptides. Mineralization systems using peptides will provide researchers with new tools for controlling various inorganic syntheses and the production of organic-inorganic materials for nanobiochemistry and materials chemistry research.

摘要

背景

肽是用于无机或有机 - 无机杂化合成(矿化)的有前景的化合物,与蛋白质相比具有若干优势。同时,基于二氧化硅的纳米材料因其在包括催化、传感、分离、酶固定以及基因和药物递送等多种技术中的潜在应用,已被广泛研究多年。在过去十年中,在理解生物硅化的分子机制以及使用肽进行图案化纳米二氧化硅的仿生合成方面取得了相当大的进展。

目的

本综述聚焦于用于二氧化硅矿化的各种肽序列,尤其是短肽序列(30个残基或更少)。

方法

我们首先简要回顾早期使用蛋白质进行二氧化硅矿化的研究以提供背景信息。随后讨论有前景的肽序列,并尝试辨别氨基酸序列、它们的矿化潜力与矿化产物性质之间的关系。

结果

使用工程蛋白(如重组硅酸酶和硅丝蛋白)对二氧化硅矿化进行合成控制,其灵感来源于生物体(海绵、硅藻和植物)中的天然蛋白介导的二氧化硅生物矿化。同时,几篇论文描述了结构良好的蛋白质组装体作为二氧化硅矿化模板的效用。这些结构良好的二氧化硅沉积物的模板导向合成最初是使用天然蛋白或蛋白质组装体(如胶原纤维和病毒空心蛋白管)进行的。然后我们综述了一系列已成功用于二氧化硅矿化的短肽(30个残基或更少)。迄今为止开发的几乎所有肽都可以像蛋白质一样按类别分类(二氧化硅矿化的合成控制或二氧化硅矿化模板的效用):第一类肽用于肽导向合成,第二类肽在组装并形成诸如纤维和管等纳米结构后用于模板导向合成。所展示的肽根据该分类进行了分类和排列。此外,我们简要介绍了由短的二氧化硅沉淀肽与模板分子组合引发的二氧化硅矿化。

结论

在本综述中,我们聚焦于为二氧化硅矿化设计的各种肽序列,尤其是30个残基或更少的短肽序列。这些肽已被用于肽导向的二氧化硅矿化和模板导向的二氧化硅矿化。本文综述的肽驱动矿化的最新进展表明,很快就有可能使用肽完全控制二氧化硅矿化过程。使用肽的矿化系统将为研究人员提供新工具,以控制各种无机合成以及用于纳米生物化学和材料化学研究的有机 - 无机材料的生产。

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