<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Richter L</submitter><funding>H2020 Excellent Science</funding><funding>Bundesbehörden der Schweizerischen Eidgenossenschaft</funding><pagination>18990-19001</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9706661</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(11)</volume><pubmed_abstract>One of the biggest threats for bacteria-based bioreactors in the biotechnology industry is infections caused by bacterial viruses called bacteriophages. More than 70% of companies admitted to encountering this problem. Despite phage infections being such a dangerous and widespread risk, to date, there are no effective methods to avoid them. Here we present a peptide-grafted compounds that irreversibly deactivate bacteriophages and remain safe for bacteria and mammalian cells. The active compounds consist of a core (cyclodextrin or gold nanoparticle) coated with a hydrophobic chain terminated with a peptide selective for bacteriophages. Such peptides were selected via a phage display technique. This approach enables irreversible deactivation of the wide range of T-like phages (including the</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Peptide-Grafted Nontoxic Cyclodextrins and Nanoparticles against Bacteriophage Infections.</pubmed_title><pmcid>PMC9706661</pmcid><funding_grant_id>754462</funding_grant_id><pubmed_authors>Stevens CA</pubmed_authors><pubmed_authors>Julia LR</pubmed_authors><pubmed_authors>Malinverni C</pubmed_authors><pubmed_authors>Stellacci F</pubmed_authors><pubmed_authors>Richter L</pubmed_authors><pubmed_authors>Wei L</pubmed_authors><pubmed_authors>Los M</pubmed_authors><pubmed_authors>Silva PJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Peptide-Grafted Nontoxic Cyclodextrins and Nanoparticles against Bacteriophage Infections.</name><description>One of the biggest threats for bacteria-based bioreactors in the biotechnology industry is infections caused by bacterial viruses called bacteriophages. More than 70% of companies admitted to encountering this problem. Despite phage infections being such a dangerous and widespread risk, to date, there are no effective methods to avoid them. Here we present a peptide-grafted compounds that irreversibly deactivate bacteriophages and remain safe for bacteria and mammalian cells. The active compounds consist of a core (cyclodextrin or gold nanoparticle) coated with a hydrophobic chain terminated with a peptide selective for bacteriophages. Such peptides were selected via a phage display technique. This approach enables irreversible deactivation of the wide range of T-like phages (including the</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-05T09:43:27.834Z</modification><creation>2025-04-05T09:43:27.834Z</creation></dates><accession>S-EPMC9706661</accession><cross_references><pubmed>36259638</pubmed><doi>10.1021/acsnano.2c07896</doi></cross_references></HashMap>