Cruz Gabriela Silva, Santos Ariane Teixeira Dos, Brito Erika Helena Salles de, Rádis-Baptista Gandhi
Postgraduate Program in Pharmaceutical Sciences, Faculty of Pharmacy, Dentistry, and Nursing, Federal University of Ceara, Fortaleza 60416-030, Brazil.
Laboratory of Biochemistry and Biotechnology, Institute for Marine Sciences, Federal University of Ceara, Fortaleza 60165-081, Brazil.
Antibiotics (Basel). 2022 Dec 8;11(12):1772. doi: 10.3390/antibiotics11121772.
Cell-penetrating peptides (CPPs) are natural or engineered peptide sequences with the intrinsic ability to internalize into a diversity of cell types and simultaneously transport hydrophilic molecules and nanomaterials, of which the cellular uptake is often limited. In addition to this primordial activity of cell penetration without membrane disruption, multivalent antimicrobial activity accompanies some CPPs. Antimicrobial peptides (AMPs) with cell-penetrability exert their effect intracellularly, and they are of great interest. CPPs with antimicrobial activity (CPAPs) comprise a particular class of bioactive peptides that arise as promising agents against difficult-to-treat intracellular infections. This short review aims to present the antibacterial, antiparasitic, and antiviral effects of various cell-penetrating antimicrobial peptides currently documented. Examples include the antimicrobial effects of different CPAPs against bacteria that can propagate intracellularly, like sp., sp., s, , sp., sp., sp. among others. CPAPs with antiviral effects that interfere with the intracellular replication of HIV, hepatitis B, HPV, and herpes virus. Additionally, CPAPs with activity against protozoa of the genera , , and , the etiological agents of Leishmaniasis, Chagas' Disease, and Malaria, respectively. The information provided in this review emphasizes the potential of multivalent CPAPs, with anti-infective properties for application against various intracellular infections. So far, CPAPs bear a promise of druggability for the translational medical use of CPPs alone or in combination with chemotherapeutics. Moreover, CPAPs could be an exciting alternative for pharmaceutical design and treating intracellular infectious diseases.
细胞穿透肽(CPPs)是天然或人工设计的肽序列,具有内在能力可内化进入多种细胞类型,并同时转运亲水性分子和纳米材料,但其细胞摄取往往受到限制。除了这种不破坏膜的原始细胞穿透活性外,一些CPPs还具有多价抗菌活性。具有细胞穿透性的抗菌肽(AMPs)在细胞内发挥作用,备受关注。具有抗菌活性的CPPs(CPAPs)构成了一类特殊的生物活性肽,有望成为对抗难治性细胞内感染的药物。这篇简短综述旨在介绍目前已记录的各种细胞穿透抗菌肽的抗菌、抗寄生虫和抗病毒作用。实例包括不同CPAPs对可在细胞内繁殖的细菌的抗菌作用,如 菌、 菌、 菌、 菌、 菌、 菌、 菌等。具有抗病毒作用的CPAPs可干扰HIV、乙型肝炎、人乳头瘤病毒和疱疹病毒的细胞内复制。此外,CPAPs对 属、 属和 属的原生动物具有活性,分别是利什曼病、恰加斯病和疟疾的病原体。本综述提供的信息强调了多价CPAPs在对抗各种细胞内感染方面的抗感染特性的潜力。到目前为止,CPAPs有望单独或与化疗药物联合用于CPPs的转化医学应用。此外,CPAPs可能是药物设计和治疗细胞内传染病的一个令人兴奋的替代方案。