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基于 DNA 的合成生长因子类似物,具有精细调控的激动作用*。

DNA-Based Synthetic Growth Factor Surrogates with Fine-Tuned Agonism*.

机构信息

Department of Chemistry and Biotechnology, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.

Cellular Informatics Laboratory, RIKEN Cluster for Pioneering Research, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan.

出版信息

Angew Chem Int Ed Engl. 2021 Oct 11;60(42):22745-22752. doi: 10.1002/anie.202105314. Epub 2021 Jul 29.


DOI:10.1002/anie.202105314
PMID:34142433
Abstract

Designing synthetic surrogates of functional proteins is an important, albeit challenging, task in the field of chemistry. A strategy toward the design of synthetic agonists for growth factor or cytokine receptors that elicit a desired signal activity has been in high demand, as such ligands hold great promise as safer and more effective therapeutics. In the present study, we used a DNA aptamer as a building block and described the strategy-guided design of a synthetic receptor agonist with fine-tuned agonism. The developed synthetic partial agonist can regulate therapeutically relevant cellular activities by eliciting fine-tuned receptor signaling.

摘要

设计功能性蛋白质的合成类似物是化学领域的一项重要但具有挑战性的任务。设计生长因子或细胞因子受体的合成激动剂的策略一直受到高度需求,因为这些配体作为更安全、更有效的治疗方法具有巨大的潜力。在本研究中,我们使用 DNA 适体作为构建块,并描述了具有精细调节激动作用的合成受体激动剂的策略指导设计。开发的合成部分激动剂可以通过引发精细调节的受体信号来调节治疗相关的细胞活性。

相似文献

[1]
DNA-Based Synthetic Growth Factor Surrogates with Fine-Tuned Agonism*.

Angew Chem Int Ed Engl. 2021-10-11

[2]
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PLoS One. 2015-12-11

[3]
A chemically unmodified agonistic DNA with growth factor functionality for in vivo therapeutic application.

Sci Adv. 2020-4-1

[4]
Bispecific Aptamer Induced Artificial Protein-Pairing: A Strategy for Selective Inhibition of Receptor Function.

J Am Chem Soc. 2019-8-5

[5]
Logic-Gate-Actuated DNA-Controlled Receptor Assembly for the Programmable Modulation of Cellular Signal Transduction.

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[6]
Nongenetic Approach for Imaging Protein Dimerization by Aptamer Recognition and Proximity-Induced DNA Assembly.

J Am Chem Soc. 2018-3-13

[7]
A DNA aptamer to c-Met inhibits cancer cell migration.

Chem Commun (Camb). 2014-11-7

[8]
Nongenetic Reprogramming of the Ligand Specificity of Growth Factor Receptors by Bispecific DNA Aptamers.

J Am Chem Soc. 2017-5-8

[9]
Artificial human Met agonists based on macrocycle scaffolds.

Nat Commun. 2015-3-11

[10]
An engineered dimeric fragment of hepatocyte growth factor is a potent c-MET agonist.

FEBS Lett. 2014-12-20

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[2]
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[3]
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[4]
DNA-modulated dimerization and oligomerization of cell membrane receptors.

Chem Commun (Camb). 2024-9-16

[5]
Cell Membrane-Anchored DNA Nanoinhibitor for Inhibition of Receptor Tyrosine Kinase Signaling Pathways via Steric Hindrance and Lysosome-Induced Protein Degradation.

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[6]
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[7]
Current Advances in Aptamer-based Biomolecular Recognition and Biological Process Regulation.

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