Peptide‐Peptide Nucleic Acid Hybrid Hydrogel Based on Sequence Programmable Morphological Change for DNA Data Storage

IF 8.9
Huiling Lei, Jinsheng Li, Zixiao Zhang, Zi’an Lin, Guangxu Zhang, Jianjian Huang, Shuhan Dai, Guojiao Wu, Hongmei Liu, Yuzhou Wu
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引用次数: 0

Abstract

Peptide‐based hydrogels provide biocompatible, stimuli‐responsive platforms, while peptide‐DNA hybrids extend programmability through hybridization‐driven crosslinking. However, nucleobase incorporation can influence peptide self‐assembly pathways. We demonstrate that the introduction of bases can directly alter the transition of peptides between gel and solution, offering an alternative mechanism to hybridization‐dependent approaches. Using peptide nucleic acid–guanine as a molecular bridge, guanine attachment shifts peptide assemblies from gel to solution states. Conversely, introducing complementary cytosine‐rich DNA sequences triggers a solution‐to‐gel transition. This morphological switching is sequence‐specific, enabling precise spatiotemporal control of gelation. Structural and rheological analyses confirm guanine's critical role in altering peptide backbone organization and enabling dynamic reconfiguration. As a demonstration of this programmable material's capabilities, we applied the hydrogel for DNA data storage. The hydrogel protects encapsulated DNA information from enzymatic degradation and facilitates precise digital information retrieval, establishing a robust storage medium for synthetic DNA‐encoded data. This strategy leverages nucleic acid sequence specificity to directly manipulate peptide nanostructure, advancing the design of smart, stimuli‐responsive biomaterials.
基于序列可编程形态变化的肽-肽核酸杂交水凝胶用于DNA数据存储
肽基水凝胶提供了生物相容性,刺激响应平台,而肽- DNA杂交通过杂交驱动的交联扩展了可编程性。然而,核碱基掺入可以影响肽的自组装途径。我们证明,碱基的引入可以直接改变凝胶和溶液之间肽的转变,为依赖杂交的方法提供了一种替代机制。利用肽核酸-鸟嘌呤作为分子桥,鸟嘌呤附着将肽组装从凝胶状态转移到溶液状态。相反,引入互补的富含胞嘧啶的DNA序列会触发溶液到凝胶的转变。这种形态转换是序列特异性的,可以精确地控制凝胶的时空。结构和流变分析证实了鸟嘌呤在改变肽主干组织和实现动态重构中的关键作用。为了证明这种可编程材料的能力,我们将水凝胶应用于DNA数据存储。水凝胶保护封装的DNA信息免受酶降解,促进精确的数字信息检索,为合成DNA编码数据建立一个强大的存储介质。该策略利用核酸序列特异性直接操纵肽纳米结构,推进智能刺激响应生物材料的设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.30
自引率
0.00%
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