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工程化结蛋白肽作为诊断试剂、治疗药物和药物递送载体。

Engineered knottin peptides as diagnostics, therapeutics, and drug delivery vehicles.

作者信息

Kintzing James R, Cochran Jennifer R

机构信息

Department of Bioengineering, Stanford University, United States.

Department of Bioengineering, Stanford University, United States; Department of Chemical Engineering, Stanford University, United States.

出版信息

Curr Opin Chem Biol. 2016 Oct;34:143-150. doi: 10.1016/j.cbpa.2016.08.022. Epub 2016 Sep 16.

Abstract

Inhibitor cystine-knots, also known as knottins, are a structural family of ultra-stable peptides with diverse functions. Knottins and related backbone-cyclized peptides called cyclotides contain three disulfide bonds connected in a particular arrangement that endows these peptides with high thermal, proteolytic, and chemical stability. Knottins have gained interest as candidates for non-invasive molecular imaging and for drug development as they can possess the pharmacological properties of small molecules and the target affinity and selectively of protein biologics. Naturally occurring knottins are clinically approved for treating chronic pain and GI disorders. Combinatorial methods are being used to engineer knottins that can bind to other clinically relevant targets in cancer, and inflammatory and cardiac disease. This review details recent examples of engineered knottin peptides; their use as molecular imaging agents, therapeutics, and drug delivery vehicles; modifications that can be introduced to improve peptide folding and bioactivity; and future perspectives and challenges in the field.

摘要

抑制性胱氨酸结,也称为结蛋白,是一类具有多种功能的超稳定肽结构家族。结蛋白和称为环肽的相关主链环化肽含有以特定排列连接的三个二硫键,赋予这些肽高热稳定性、蛋白水解稳定性和化学稳定性。由于结蛋白可具有小分子的药理特性以及蛋白质生物制剂的靶标亲和力和选择性,因此作为非侵入性分子成像候选物和药物开发的候选物受到关注。天然存在的结蛋白已被临床批准用于治疗慢性疼痛和胃肠道疾病。正在使用组合方法来设计能够结合癌症、炎症和心脏病中其他临床相关靶标的结蛋白。本综述详细介绍了工程化结蛋白肽的最新实例;它们作为分子成像剂、治疗剂和药物递送载体的用途;为改善肽折叠和生物活性可引入的修饰;以及该领域的未来前景和挑战。

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