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2
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Future Med Chem. 2015;7(16):2091-3. doi: 10.4155/fmc.15.147. Epub 2015 Oct 29.
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Sensing Protein Surfaces with Targeted Fluorescent Receptors.利用靶向荧光受体感知蛋白质表面
Chemistry. 2015 Nov 2;21(45):15981-7. doi: 10.1002/chem.201502069. Epub 2015 Sep 18.
4
A Modular, DNA-Based Beacon for Single-Step Fluorescence Detection of Antibodies and Other Proteins.一种基于DNA的模块化信标,用于抗体和其他蛋白质的单步荧光检测。
Angew Chem Int Ed Engl. 2015 Nov 2;54(45):13214-8. doi: 10.1002/anie.201505179. Epub 2015 Sep 4.
5
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J Am Chem Soc. 2015 Aug 5;137(30):9507-10. doi: 10.1021/jacs.5b01123. Epub 2015 Jun 23.
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Identification of structure-activity relationships from screening a structurally compact DNA-encoded chemical library.从结构紧凑的 DNA 编码化学文库筛选中鉴定结构-活性关系。
Angew Chem Int Ed Engl. 2015 Mar 23;54(13):3927-31. doi: 10.1002/anie.201410736. Epub 2015 Feb 3.
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Targeted protein surface sensors as a tool for analyzing small populations of proteins in biological mixtures.靶向蛋白表面传感器作为一种分析生物混合物中小群体蛋白的工具。
Angew Chem Int Ed Engl. 2014 Aug 25;53(35):9289-93. doi: 10.1002/anie.201402501. Epub 2014 May 19.
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Oligonucleotide-Based Systems for Input-Controlled and Non-Covalently Regulated Protein-Binding.用于输入控制和非共价调节蛋白质结合的基于寡核苷酸的系统。
Supramol Chem. 2013 Jan 1;25(12). doi: 10.1080/10610278.2013.810337.
9
Manipulating signaling at will: chemically-inducible dimerization (CID) techniques resolve problems in cell biology.随心所欲地操控信号:化学诱导二聚体(CID)技术解决了细胞生物学中的问题。
Pflugers Arch. 2013 Mar;465(3):409-17. doi: 10.1007/s00424-012-1208-6. Epub 2013 Jan 9.
10
A logical molecular circuit for programmable and autonomous regulation of protein activity using DNA aptamer-protein interactions.使用 DNA 适体-蛋白相互作用的可编程和自主调节蛋白质活性的逻辑分子电路。
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模拟信号蛋白的功能:迈向人工信号转导治疗

Mimicking the Function of Signaling Proteins: Toward Artificial Signal Transduction Therapy.

作者信息

Peri-Naor Ronny, Motiei Leila, Margulies David

机构信息

Department of Organic Chemistry, Weizmann Institute of Science.

Department of Organic Chemistry, Weizmann Institute of Science;

出版信息

J Vis Exp. 2016 Sep 29(115):54396. doi: 10.3791/54396.

DOI:10.3791/54396
PMID:27768030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5092080/
Abstract

Signal transduction pathways, which control the response of cells to various environmental signals, are mediated by the function of signaling proteins that interact with each other and activate one other with high specificity. Synthetic agents that mimic the function of these proteins might therefore be used to generate unnatural signal transduction steps and consequently, alter the cell's function. We present guidelines for designing 'chemical transducers' that can induce artificial communication between native proteins. In addition, we present detailed protocols for synthesizing and testing a specific 'transducer', which can induce communication between two unrelated proteins: platelet-derived growth-factor (PDGF) and glutathione-S-transferase (GST). The way by which this unnatural PDGF-GST communication could be used to control the cleavage of an anticancer prodrug is also presented, indicating the potential for using such systems in 'artificial signal transduction therapy'. This work is intended to facilitate developing additional 'transducers' of this class, which may be used to mediate intracellular protein-protein communication and consequently, to induce artificial cell signaling pathways.

摘要

信号转导通路控制细胞对各种环境信号的反应,由相互作用并以高特异性相互激活的信号蛋白的功能介导。因此,模拟这些蛋白质功能的合成剂可能用于产生非天然的信号转导步骤,从而改变细胞功能。我们提出了设计“化学换能器”的指导方针,该换能器可诱导天然蛋白质之间的人工通讯。此外,我们还给出了合成和测试一种特定“换能器”的详细方案,该换能器可诱导两种不相关蛋白质之间的通讯:血小板衍生生长因子(PDGF)和谷胱甘肽-S-转移酶(GST)。还介绍了这种非天然的PDGF-GST通讯可用于控制抗癌前药裂解的方式,表明了在“人工信号转导疗法”中使用此类系统的潜力。这项工作旨在促进开发此类额外的“换能器”,其可用于介导细胞内蛋白质-蛋白质通讯,从而诱导人工细胞信号通路。