Department of Chemistry, University of South Florida, 4202 E. Fowler Ave, Tampa, FL 33620, United States.
Curr Med Chem. 2019;26(13):2313-2329. doi: 10.2174/0929867324666171107095913.
A new class of peptidomimetics termed as "γ-AApeptides" was recently developed by our group. Similar to other peptidomimetics, γ-AApeptides are resistant to proteolytic degradation, and possess limitless potential to introduce chemically diverse functional groups. γ-AApeptides have shown great promise in biomedical applications. In this article, we will review a few examples of γ-AApeptides with biological potential. Certain γ-AApeptides can permeate cell membranes and therefore they can be used as potential drug carrier. γ-AApeptides can also bind to HIV RNA with high specificity and affinity, suggesting their potential application as anti-HIV agents. Moreover, they can mimic host-defense peptides and display potent and broad-spectrum activity towards a range of drug-resistant bacterial pathogens. They are also potential anti-cancer agents. For instance, they have shown great promise in targeted imaging of tumor in mouse model, and they are also capable of disrupting p53/DNA interactions, and thus antagonize STAT3 signaling pathway. Recently, from combinatorial screening, γ-AApeptides are identified to inhibit Aβ peptide aggregation, and thus they can be developed into potential anti- Alzheimer's disease agent.
最近,我们小组开发了一类被称为“γ-AA 肽”的新型肽类似物。与其他肽类似物一样,γ-AA 肽不易被蛋白水解降解,并且具有引入化学结构多样化的官能团的无限潜力。γ-AA 肽在生物医学应用中具有广阔的前景。在本文中,我们将回顾一些具有生物潜力的 γ-AA 肽的例子。某些 γ-AA 肽可以穿透细胞膜,因此可以用作潜在的药物载体。γ-AA 肽还可以与 HIV RNA 高度特异性和亲和力结合,表明它们可能作为抗 HIV 药物的应用。此外,它们可以模拟宿主防御肽,并对一系列耐药细菌病原体显示出强大且广谱的活性。它们也是潜在的抗癌药物。例如,它们在靶向成像肿瘤的小鼠模型中显示出巨大的应用潜力,并且能够破坏 p53/DNA 相互作用,从而拮抗 STAT3 信号通路。最近,通过组合筛选,发现 γ-AA 肽可以抑制 Aβ 肽聚集,因此可以开发成潜在的抗阿尔茨海默病药物。