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适配子对抗细胞表面受体:筛选、修饰及应用。

Aptamers against cell surface receptors: selection, modification and application.

机构信息

Department of Biochemistry and National Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, 210093 Nanjing, China.

出版信息

Curr Med Chem. 2011;18(27):4107-16. doi: 10.2174/092986711797189628.

Abstract

Aptamers are synthetic oligonucleotides selected from pools of random-sequence oligonucleotides which bind to a wide range of biomolecular targets with high affinity and specificity. Compared with antibodies, aptamers exhibit significant advantages including small size, easy synthesis and modification, as well as low immunogenicity. Many of the aptamers also show inhibition of their targets, making them potential therapeutic and targeting reagents in clinical applications. Compared with aptamers against intracellular proteins and molecules, however, the identification of aptamers against cell-surface receptors and receptor-related antigens is more difficult, due to the complex cellular environment in which receptors are located, and also the unique conformations and compositions of receptors to keep their activity. In this review, we will introduce the identification, modification and working mechanism of aptamers against cell-surface receptors. Based on the different characteristics of target receptors and selection strategies used, the identified aptamers show distinct binding affinity with recombinant targets or specific cell lines which express receptors on the surface in vitro. Some of the in vivo experiments also indicate that aptamers have the capability of inhibiting the overexpressing receptor-related tumor growth, working as potential anti-tumor therapeutic drugs. Despite of the difficulties during the selection of receptor aptamers and the study of their working mechanism during the present time, it is possible that in the future aptamers will increasingly exhibit therapeutic and diagnostic utility.

摘要

适配体是从随机序列寡核苷酸库中筛选出的合成寡核苷酸,能与多种生物分子靶标高亲和力和特异性结合。与抗体相比,适配体具有体积小、易于合成和修饰以及免疫原性低等显著优势。许多适配体还具有抑制其靶标的作用,使其成为临床应用中具有潜力的治疗和靶向试剂。然而,与针对细胞内蛋白质和分子的适配体相比,针对细胞表面受体和受体相关抗原的适配体的鉴定更为困难,这是由于受体所处的复杂细胞环境,以及受体保持其活性的独特构象和组成。在这篇综述中,我们将介绍针对细胞表面受体的适配体的鉴定、修饰和作用机制。基于不同的靶受体特征和所使用的选择策略,所鉴定的适配体与体外表达受体的重组靶标或特定细胞系表现出不同的结合亲和力。一些体内实验也表明,适配体具有抑制过表达受体相关肿瘤生长的能力,可作为潜在的抗肿瘤治疗药物。尽管目前在受体适配体的选择和作用机制研究方面存在困难,但将来适配体可能会越来越多地表现出治疗和诊断的应用潜力。

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