<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(8)</volume><submitter>Du RL</submitter><funding>Hong Kong Polytechnic University</funding><funding>Innovation and Technology Commission</funding><pubmed_abstract>The rapid increase in bacterial resistance to conventional antibiotics has led to a great demand for novel antibacterial agents. Antimicrobial peptides (AMPs) are emerging as next-generation antimicrobial alternative drugs to conventional antibiotics because of their broad-spectrum antimicrobial activities and minimal potential for drug resistance induction. This work describes novel antimicrobial peptides (FtsZpcpp) synthesized through the conjugation of a cell penetration peptide ((RXR)&lt;sub>4&lt;/sub>XB) to nonantimicrobial peptides (FtsZp). The FtsZp peptides were previously identified to bind FtsZ (flaming-temperature-sensitive protein Z), a crucial protein in regulating bacterial cell divisions. Newly designed FtsZpcpp peptides have broad antimicrobial activities against both Gram-positi</pubmed_abstract><journal>ACS infectious diseases</journal><pagination>2190-2204</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12340945</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of Broad-Spectrum Antimicrobial Peptides through the Conjugation of FtsZ-Binding and Cell-Penetrating Peptides.</pubmed_title><pmcid>PMC12340945</pmcid><pubmed_authors>Chan PH</pubmed_authors><pubmed_authors>Kong WP</pubmed_authors><pubmed_authors>Wong KY</pubmed_authors><pubmed_authors>Du RL</pubmed_authors><pubmed_authors>Hung CH</pubmed_authors><pubmed_authors>Liang ZG</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Ding K</pubmed_authors><pubmed_authors>Leung AS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of Broad-Spectrum Antimicrobial Peptides through the Conjugation of FtsZ-Binding and Cell-Penetrating Peptides.</name><description>The rapid increase in bacterial resistance to conventional antibiotics has led to a great demand for novel antibacterial agents. Antimicrobial peptides (AMPs) are emerging as next-generation antimicrobial alternative drugs to conventional antibiotics because of their broad-spectrum antimicrobial activities and minimal potential for drug resistance induction. This work describes novel antimicrobial peptides (FtsZpcpp) synthesized through the conjugation of a cell penetration peptide ((RXR)&lt;sub>4&lt;/sub>XB) to nonantimicrobial peptides (FtsZp). The FtsZp peptides were previously identified to bind FtsZ (flaming-temperature-sensitive protein Z), a crucial protein in regulating bacterial cell divisions. Newly designed FtsZpcpp peptides have broad antimicrobial activities against both Gram-positi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-01T03:33:19.835Z</modification><creation>2026-04-07T16:35:46.946Z</creation></dates><accession>S-EPMC12340945</accession><cross_references><pubmed>40707007</pubmed><doi>10.1021/acsinfecdis.5c00220</doi></cross_references></HashMap>