Parisi Mónica G, Ozón Brenda, Vera González Sofía M, García-Pardo Javier, Obregón Walter David
Instituto de Ecología y Desarrollo Sustentable (INEDES, CONICET-UNLu) and Departamento de Ciencias Básicas, Universidad Nacional de Luján, Ruta 5 y Avenida Constitución, Luján B6700, Buenos Aires, Argentina.
Centro de Investigación de Proteínas Vegetales (CIProVe) and Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 47 y 115 s/N, La Plata B1900, Buenos Aires, Argentina.
Pharmaceutics. 2024 Apr 24;16(5):582. doi: 10.3390/pharmaceutics16050582.
Antimicrobial peptides (AMPs) are important mediator molecules of the innate defense mechanisms in a wide range of living organisms, including bacteria, mammals, and plants. Among them, peptide protease inhibitors (PPIs) from plants play a central role in their defense mechanisms by directly attacking pathogens or by modulating the plant's defense response. The growing prevalence of microbial resistance to currently available antibiotics has intensified the interest concerning these molecules as novel antimicrobial agents. In this scenario, PPIs isolated from a variety of plants have shown potential in inhibiting the growth of pathogenic bacteria, protozoans, and fungal strains, either by interfering with essential biochemical or physiological processes or by altering the permeability of biological membranes of invading organisms. Moreover, these molecules are active inhibitors of a range of proteases, including aspartic, serine, and cysteine types, with some showing particular efficacy as trypsin and chymotrypsin inhibitors. In this review, we provide a comprehensive analysis of the potential of plant-derived PPIs as novel antimicrobial molecules, highlighting their broad-spectrum antimicrobial efficacy, specificity, and minimal toxicity. These natural compounds exhibit diverse mechanisms of action and often multifunctionality, positioning them as promising molecular scaffolds for developing new therapeutic antibacterial agents.
抗菌肽(AMPs)是包括细菌、哺乳动物和植物在内的多种生物体先天防御机制的重要介导分子。其中,植物来源的肽蛋白酶抑制剂(PPI)通过直接攻击病原体或调节植物的防御反应,在其防御机制中发挥核心作用。微生物对现有抗生素的耐药性日益普遍,这增强了人们对这些分子作为新型抗菌剂的兴趣。在这种情况下,从多种植物中分离出的PPI已显示出抑制病原菌、原生动物和真菌菌株生长的潜力,其作用方式要么是干扰基本的生化或生理过程,要么是改变入侵生物体生物膜的通透性。此外,这些分子是一系列蛋白酶的活性抑制剂,包括天冬氨酸、丝氨酸和半胱氨酸类型,有些作为胰蛋白酶和胰凝乳蛋白酶抑制剂表现出特别的功效。在这篇综述中,我们全面分析了植物来源的PPI作为新型抗菌分子的潜力,突出了它们的广谱抗菌功效、特异性和低毒性。这些天然化合物表现出多样的作用机制且常常具有多功能性,使其成为开发新型治疗性抗菌剂的有前景的分子框架。