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大分子疗法:后基因组时代药物发现的新兴策略

Macromolecular therapeutics: emerging strategies for drug discovery in the postgenome era.

作者信息

Juliano R L, Astriab-Fisher A, Falke D

机构信息

Department of Pharmacology, School of Medicine and Program in Macromolecular Therapeutics, University of North Carolina, Chapel Hill 27599, USA.

出版信息

Mol Interv. 2001 Apr;1(1):40-53.

Abstract

The postgenome era offers a plethora of potential therapeutic targets. Many of these targets will be addressable using small organic molecules as drug candidates. However, certain aspects of cell function, particularly those that rely on protein-protein or protein-nucleic acid interactions, will be difficult to influence using small molecules. Thus, the possibility of using highly specific macromolecules as potential therapeutic agents is an intriguing concept. Recent developments in several areas of research have brought this possibility closer to fruition. Peptide and nucleic acid combinatorial libraries allow the generation of novel molecules having exquisite selectivity. Structural information and molecular modeling also contribute to the design of new macromolecules with therapeutic potential. Perhaps most importantly, approaches for delivering macromolecules into the cell interior have been developed and applied with considerable success. Thus, the therapeutic use of macromolecules, including oligonucleotides, peptides, and proteins, may be an idea whose time has come.

摘要

后基因组时代提供了大量潜在的治疗靶点。其中许多靶点可以使用小分子有机化合物作为候选药物来解决。然而,细胞功能的某些方面,特别是那些依赖于蛋白质-蛋白质或蛋白质-核酸相互作用的方面,将难以用小分子来影响。因此,使用高度特异性的大分子作为潜在治疗剂的可能性是一个引人入胜的概念。几个研究领域的最新进展使这种可能性更接近实现。肽和核酸组合文库能够产生具有极高选择性的新型分子。结构信息和分子建模也有助于设计具有治疗潜力的新大分子。也许最重要的是,已经开发并成功应用了将大分子递送至细胞内部的方法。因此,包括寡核苷酸、肽和蛋白质在内的大分子的治疗应用可能是一个时机已到的想法。

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