ph响应性dea衍生肽支架的设计与表征:综合分子动力学模拟研究

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS
Aditya Swaroop Chaudhary, Chandrima Modak, Bhavinkumar Gayakvad, Indrani Biswas and Alok Jain*, 
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引用次数: 0

摘要

肽基、功能活跃、刺激反应的生物材料在各种生物医学应用中具有巨大的潜力。细胞外基质(ECM)蛋白的功能活性基序,当与自组装肽(SAP)或聚合物结合时,在这种生物活性支架的开发中显示出重大的前景。然而,合成复杂性、高相关成本、有限的功能和潜在的免疫反应提出了重大挑战。本研究探索了胶原i衍生的基于gea基序的sap,结合了盐桥配对、带电和极性残基、疏水残基、淀粉样蛋白序列和非ecm基序等修饰,以开发刺激反应性、功能活性的支架。对20个系统设计的肽体系进行了16.7 μs的分子动力学(MD)模拟。这些模拟还表征了肽的刺激响应特性,重点是pH和温度响应性。在20个设计中,三个肽体系──dea - sbd、dea - sbe(盐桥修饰)和dea - f4(在c端添加疏水残基)──成功地形成了大型、稳定和生物活性的支架。与未修饰的DGEA基序相比,这些系统表现出增强的聚集性(大于90%)和改善的肽间氢键(超过30个键),同时保持功能基序的可及性(60-70%)。值得注意的是,当pH值从3.0转变为生理pH值时,dea - sbd和dea - sbe肽呈现出从小的、不稳定的、不均匀的凝胶状结构转变为大的、稳定的、均匀的、具有功能活性的支架结构。综合MD模拟研究表明,这些设计的肽在各种生理条件下均表现出聚集性增强和肽间氢键增强,同时保持其功能活性。突出了它们在生物医学应用方面的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design and Characterization of pH-Responsive DGEA-Derived Peptide Scaffolds: A Comprehensive Molecular Dynamics Simulation Study

Design and Characterization of pH-Responsive DGEA-Derived Peptide Scaffolds: A Comprehensive Molecular Dynamics Simulation Study

Peptide-based, functionally active, stimuli-responsive biomaterials hold immense potential for diverse biomedical applications. Functionally active motifs of extracellular matrix (ECM) proteins, when conjugated with self-assembling peptides (SAP) or polymers, demonstrate significant promise in the development of such bioactive scaffolds. However, synthesis complexity, high associated costs, limited functionality, and potential immune responses present significant challenges. This study explores collagen-I-derived DGEA motif-based SAPs, incorporating modifications such as salt bridge pairing, charged and polar residues, hydrophobic residues, amyloidogenic sequences, and non-ECM motifs, to develop stimuli-responsive, functionally active scaffolds. Extensive molecular dynamics (MD) simulations, totaling 16.7 μs, were conducted on 20 systematically designed peptide systems. These simulations also characterized the stimuli-responsive properties of the peptides, focusing on pH and temperature responsiveness. Among the 20 designs, three peptide systems─DGEA-SBD, DGEA-SBE (salt-bridge modifications), and DGEA-F4 (with hydrophobic residue addition at the C-terminus)─successfully formed large, stable, and bioactive scaffolds. These systems exhibited enhanced aggregation (greater than 90%) and improved interpeptide hydrogen bonding (more than 30 bonds) while maintaining the accessibility of functional motifs (60–70% availability) compared to the unmodified DGEA motif. Notably, the DGEA-SBD and DGEA-SBE peptides showed a transition from small, unstable, uneven gel-like structures to large, stable, uniform, and functionally active scaffolds as the pH shifted from 3.0 to physiological pH. Comprehensive MD simulation studies demonstrated that these designed peptides exhibit increased aggregation and enhanced interpeptide hydrogen bonding while retaining their functional activity under various physiological conditions, highlighting their promising potential for biomedical applications.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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