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用于评估炭疽保护性抗原和致死因子相互作用的治疗应用的预测和荧光纳米传感实验方法。

Predictive and fluorescent nanosensing experimental methods for evaluating anthrax protective antigen and lethal factor interactions for therapeutic applications.

机构信息

Department of Biotechnology, Faculty of Science, University of Maragheh, P.O. Box 55181-83111, Maragheh, Iran.

Department of Biotechnology, Faculty of Science, University of Maragheh, P.O. Box 55181-83111, Maragheh, Iran.

出版信息

Int J Biol Macromol. 2020 Oct 1;160:1158-1167. doi: 10.1016/j.ijbiomac.2020.05.190. Epub 2020 May 25.

Abstract

Recently, specific interaction of anthrax protective antigen domain 4 (PAD4) and lethal factor domain 1 (LFD1) have been considered for the design of novel diagnostic and therapeutic systems in medicine. In this study, theoretical and experimental approaches were used to monitor the interactions of PAD4 and LFD1. CLusPro server and Dimplot software were used to predict the interaction of these domains. Results, revealed interactive sites between PAD4 and LFD1 on loop regions of both C and N terminal of PAD4. In experimental methods, PAD4 and LFD1 were expressed in Escherichia coli and purified for usage in Magnetic Bead (MB) and Multi-Walled Carbon Nanotubes (MWCNTs) based bio-sensing platforms. In the magnetic-based system, the magnetic sedimentation of QD-PAD4 by MBs-LFD1 and the observation of the fluorescence spectrum related to QD-PAD4 in the precipitated materials confirmed the interaction of PAD4 with LFD1 protein. In the MWCNTs-based method, the QD-PAD4 fluorescence was quenched by absorption on MWCNTs. Upon the addition of LFD1, fluorescence emission was recovered, indicating interaction of LFD1 with QD-PAD4, which results the separation of QD-PAD4 from MWCNTs surfaces and fluorescence restoration. Finally, new approaches showed the interaction of PAD4 and LFD1, which can be used as an attractive model in medicine.

摘要

最近,炭疽保护性抗原结构域 4(PAD4)和致死因子结构域 1(LFD1)的特定相互作用已被认为是医学中设计新型诊断和治疗系统的基础。在这项研究中,采用理论和实验方法来监测 PAD4 和 LFD1 的相互作用。CLusPro 服务器和 Dimplot 软件被用于预测这些结构域的相互作用。结果表明,PAD4 和 LFD1 在 PAD4 的 C 端和 N 端的环区之间存在相互作用位点。在实验方法中,PAD4 和 LFD1 在大肠杆菌中表达并纯化,用于基于磁珠(MB)和多壁碳纳米管(MWCNTs)的生物传感平台。在基于磁性的系统中,MBs-LFD1 通过磁性沉淀 QD-PAD4,以及观察沉淀材料中与 QD-PAD4 相关的荧光光谱,证实了 PAD4 与 LFD1 蛋白的相互作用。在基于 MWCNTs 的方法中,MWCNTs 上的吸收使 QD-PAD4 的荧光猝灭。加入 LFD1 后,荧光发射恢复,表明 LFD1 与 QD-PAD4 相互作用,导致 QD-PAD4 从 MWCNTs 表面分离并恢复荧光。最后,新方法显示了 PAD4 和 LFD1 的相互作用,可作为医学上有吸引力的模型。

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