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适体及其选择性靶向表皮生长因子(EGF)、Wnt/β-连环蛋白和转化生长因子β(TGFβ)-Smad家族信号传导各方面的潜力。

Aptamers and their potential to selectively target aspects of EGF, Wnt/β-catenin and TGFβ-smad family signaling.

作者信息

Conidi Andrea, van den Berghe Veronique, Huylebroeck Danny

机构信息

Laboratory of Molecular Biology (Celgen), Department of Development and Regeneration, KU Leuven, Campus Gasthuisberg, Building Ond & Nav4 p.o.box 812, room 05.313, Stem Cell Institute, Herestraat 49, B-3000 Leuven, Belgium.

出版信息

Int J Mol Sci. 2013 Mar 26;14(4):6690-719. doi: 10.3390/ijms14046690.

Abstract

The smooth identification and low-cost production of highly specific agents that interfere with signaling cascades by targeting an active domain in surface receptors, cytoplasmic and nuclear effector proteins, remain important challenges in biomedical research. We propose that peptide aptamers can provide a very useful and new alternative for interfering with protein-protein interactions in intracellular signal transduction cascades, including those emanating from activated receptors for growth factors. By their targeting of short, linear motif type of interactions, peptide aptamers have joined nucleic acid aptamers for use in signaling studies because of their ease of production, their stability, their high specificity and affinity for individual target proteins, and their use in high-throughput screening protocols. Furthermore, they are entering clinical trials for treatment of several complex, pathological conditions. Here, we present a brief survey of the use of aptamers in signaling pathways, in particular of polypeptide growth factors, starting with the published as well as potential applications of aptamers targeting Epidermal Growth Factor Receptor signaling. We then discuss the opportunities for using aptamers in other complex pathways, including Wnt/β-catenin, and focus on Transforming Growth Factor-β/Smad family signaling.

摘要

通过靶向表面受体、细胞质和核效应蛋白中的活性结构域来干扰信号级联反应的高特异性试剂的顺利鉴定和低成本生产,仍然是生物医学研究中的重要挑战。我们提出,肽适配体可以为干扰细胞内信号转导级联反应中的蛋白质-蛋白质相互作用提供一种非常有用的新方法,包括那些源自生长因子激活受体的相互作用。由于肽适配体靶向短的线性基序类型的相互作用,它们易于生产、稳定性高、对单个靶蛋白具有高特异性和亲和力,并且可用于高通量筛选方案,因此已与核酸适配体一起用于信号研究。此外,它们正在进入治疗几种复杂病理状况的临床试验。在此,我们简要概述适配体在信号通路中的应用,特别是在多肽生长因子方面,从靶向表皮生长因子受体信号的适配体的已发表应用以及潜在应用开始。然后我们讨论在其他复杂通路中使用适配体的机会,包括Wnt/β-连环蛋白通路,并重点关注转化生长因子-β/Smad家族信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6c/3645661/bd87ac6620d4/ijms-14-06690f1.jpg

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