Lipidation of a nuclear localization sequence enhances broad-spectrum antimicrobial activity: synthesis, characterization, and in silico analysis
(MIC = 6.96 µM), while LP-3 and LP-4 demonstrated moderate, broad-spectrum activity. Computational analyses indicated favorable target interactions, though they did not fully correlate with experimental results. LP-4 and LP-5 showed the smallest HOMO-LUMO gaps (∼0.111-0.112 eV), suggesting higher electronic reactivity. Overall, lipidation of PKKKRKV is a promising strategy for developing antimicrobial agents. Chain length and saturation significantly influence activity, with LP-5 emerging as the most promising broad-spectrum candidate. Further studies are required to validate mechanisms and assess toxicity..
Authors
- Muhamad Imam Muhajir
- Reza Aditama (ORCID: https://orcid.org/0009-0006-1797-1059)
- Taufik Muhammad Fakih (ORCID: https://orcid.org/0000-0001-7155-4412)
- Tarwadi Tarwadi (ORCID: https://orcid.org/0000-0002-9915-6739)
- Ace Tatang Hidayat (ORCID: https://orcid.org/0000-0002-6960-3825)
- Rani Maharani
- Anggun Fuji Rizqiyani
- Doddy Irawan Setyo Utomo
Institutions
- Bandung Institute of Technology (ID)
- University of Indonesia (ID)
- Institut de Recherche Vaccinale (FR)
- Bandung Islamic University (ID)
- Padjadjaran University (ID)
Publication Details
- Journal
- Artificial Cells Nanomedicine and Biotechnology
- Published
- 2026-03-31
- DOI
- https://doi.org/10.1080/21691401.2026.2649071
- Primary Topic
- Antimicrobial Peptides and Activities
- Type
- article
- Field-Weighted Citation Impact
- 0.00