TABLE 3.
Most representative examples of self-assembled AMPs.
| AMP | Sequence | Self-assembling | Antimicrobial activity | Tested microorganisms | Special functions | References |
| Diphenylalanine peptide | FF | Aromatic stacking | MIC: 125 μg/ml | E. coli | It is the smallest model for antibacterial supramolecular polymers | Schnaider et al., 2017 |
| Fmoc-peptide gelator | Fmoc-FF-Py + | Aromatic stacking | MIC: 10 μg/ml | S. aureus | − | Debnath et al., 2010 |
| Fmoc-peptide gelators | NapFFKK | Aromatic stacking | − | E. coli and S. epidermidis | Reduces the viable S. epidermidis biofilm by 94% | Laverty et al., 2014 |
| Tripeptide | DLFF | Aromatic stacking | − | E. coli, Klebsiella pneumoniae, and S. aureus | Shows the antibiotic delivery capacity, has a mild antimicrobial activity against the Gram-negative strains | Marchesan et al., 2013 |
| HHC-10 | KRWWKWIRW-NH2 | Aromatic stacking | MIC: 8 μM/ml | S. aureus | Causes aggregation of bacteria at higher concentrations | Bagheri et al., 2020 |
| A9K | AAAAAAAAAK | Hydrophobic forces | A9K with concentration of 0.1 mg/ml inhibits the bacterial growth after an incubation of 1 h (survival rate < 20%) | E. coli and S. aureus | − | Chen C. et al., 2010 |
| RA9R | RAAAAAAAAAR | Hydrophobic forces | The concentration to 0.1 wt% RA9R reduces the CFU with 2.6, 3.4, and 4.0 orders of magnitude for microbes tested, respectively, after 24 h incubation | S. aureus, P. aeruginosa, and P. syringae | − | Edwards-Gayle et al., 2019 |
| RADA16-Tet213 | RADARADARA DARADA-KRWWKWWRRC | Electrostatic interactions and hydrophobic forces | RADA16-Tet213 with concentration of 1 mg/ml eliminates the bacterial cells after 12 h incubation (OD600 < 0.3) | S. aureus | Has been applied for controlled release delivery of AMPs, promotes the proliferation of bone mesenchymal stem cells | Yang et al., 2018 |
| KLD-3R | RRRKLDL KLDLKLDL | Electrostatic interactions and hydrophobic forces | MIC: 5—6 μM/ml | E. coli, S. aureus, B. subtilis, P. aeruginosa | Improves osteogenic property and enhances bone regeneration in vivo in a fracture model. | Tripathi et al., 2015 |
| K3W (QL)6K2 | KKKWQLQLQ LQLQLQLKK | Intermolecular hydrogen bonding and hydrophobic forces | MIC: 5—20 μM/ml | E. coli, P. aeruginosa, S. aureus, and S. epidermidis | Reduces the cytotoxicity on mouse bone marrow-derived monocytes, improves the stability in trypsin and chymotrypsin solutions | Lam et al., 2016 |
| Octapeptide | IKFQFHFD | Intermolecular hydrogen bonding, electrostatic interactions, | MIC: 3 mg/ml at pH 5.5 | S. aureus | Shows the multiple drug | Wang et al., 2019a |
| hydrophobic forces, and aromatic stacking | delivery capacity, exhibits acidic pH-switchable broad-spectrum antimicrobial effect via a mechanism involving cell wall and membrane disruption | |||||
| P11-28/29 | QQRFEWEFEQQ-NH2//OQOFO WOFOQO-NH2 | Intermolecular hydrogen bonding, electrostatic interactions, and aromatic stacking | P11-28/29 with concentration of 10 mg/ml inhibits the bacterial growth after an incubation of 48 h (bacterial growth < 50%) | P. gingivalis, S. sanguinis | Shows the antibiotic delivery capacity, enables to strengthen the osteogenic differentiation of human dental follicle stem cells | Koch et al., 2019 |
| Human α-defensin 6 (H25W) | AFTCHCRRS CYSTEYSYGTCT VMGINWRFCCL | − | MIC: 32 μg/ml | Bifidobacterium adolescentis | Entraps microbes and prevent invasive gastrointestinal pathogens such as Salmonella enterica serovar Typhimurium and Listeria monocytogenes from entering host cells | Chu et al., 2012; Schroeder et al., 2015 |