Matches in SemOpenAlex for { <https://semopenalex.org/work/W2083669011> ?p ?o ?g. }
- W2083669011 abstract "The spore-forming gut bacterium Clostridium difficile is the leading cause of antibiotic-associated diarrhea in hospitalized patients. The major virulence factors are two large glucosylating cytotoxins. Hypervirulent strains (e.g. ribotype 027) with higher morbidity and mortality additionally produce the binary CDT toxin (Clostridium difficile transferase) that ADP-ribosylates actin and induces microtubule-based cell protrusions. Nanobodies are robust single domain antibodies derived from camelid heavy chain antibodies. Here we report the generation of functional nanobodies against the enzymatic CDTa and the heptameric receptor binding subunit CDTb. The nanobodies were obtained from a variable-domain repertoire library isolated from llamas immunized with recombinant CDTa or CDTb. Five CDTa-specific nanobodies blocked CDTa-mediated ADP-ribosylation of actin. Three CDTa-specific and two CDTb-specific nanobodies neutralized the cytotoxicity of CDTa+b. These nanobodies hold promise as new tools for research, diagnosis and therapy of C. difficile associated disease." @default.
- W2083669011 created "2016-06-24" @default.
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- W2083669011 date "2015-01-19" @default.
- W2083669011 modified "2023-09-23" @default.
- W2083669011 title "Selection of Nanobodies that Block the Enzymatic and Cytotoxic Activities of the Binary Clostridium Difficile Toxin CDT" @default.
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- W2083669011 doi "https://doi.org/10.1038/srep07850" @default.
- W2083669011 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4297958" @default.
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