دورية أكاديمية
Botulinum Neurotoxin F Subtypes Cleaving the VAMP-2 Q58⁻K59 Peptide Bond Exhibit Unique Catalytic Properties and Substrate Specificities
| العنوان: | Botulinum Neurotoxin F Subtypes Cleaving the VAMP-2 Q58⁻K59 Peptide Bond Exhibit Unique Catalytic Properties and Substrate Specificities |
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| المؤلفون: | Sikorra, Stefan, Skiba, Martin, Dorner, Martin B, Weisemann, Jasmin, Weil, Mirjam, Valdezate, Sylvia, Davletov, Bazbek, Rummel, Andreas, Dorner, Brigitte G, Binz, Thomas |
| المساهمون: | Deutsche Forschungsgemeinschaft (Alemania), Federal Ministry of Education & Research (Alemania) |
| بيانات النشر: | Multidisciplinary Digital Publishing Institute (MDPI) |
| سنة النشر: | 2018 |
| المجموعة: | REPISALUD (REPositorio Institucional en SALUD del Instituto de Salud Carlos III - ISCIII) |
| مصطلحات موضوعية: | Clostridium botulinum, Zn2+ protease, Botulinum neurotoxin, Serotype F, Subtype, Synaptobrevin, Vesicle associated membrane protein 2 (VAMP-2), Botulinum Toxins, Catalysis, Peptides, Substrate Specificity, Vesicle-Associated Membrane Protein 2 |
| الوصف: | In the recent past, about 40 botulinum neurotoxin (BoNT) subtypes belonging to serotypes A, B, E, and F pathogenic to humans were identified among hundreds of independent isolates. BoNTs are the etiological factors of botulism and represent potential bioweapons; however, they are also recognized pharmaceuticals for the efficient counteraction of hyperactive nerve terminals in a variety of human diseases. The detailed biochemical characterization of subtypes as the basis for development of suitable countermeasures and possible novel therapeutic applications is lagging behind the increase in new subtypes. Here, we report the primary structure of a ninth subtype of BoNT/F. Its amino-acid sequence diverges by at least 8.4% at the holotoxin and 13.4% at the enzymatic domain level from all other known BoNT/F subtypes. We found that BoNT/F9 shares the scissile Q58/K59 bond in its substrate vesicle associated membrane protein 2 with the prototype BoNT/F1. Comparative biochemical analyses of four BoNT/F enzymatic domains showed that the catalytic efficiencies decrease in the order F1 > F7 > F9 > F6, and vary by up to a factor of eight. KM values increase in the order F1 > F9 > F6 ≈ F7, whereas kcat decreases in the order F7 > F1 > F9 > F6. Comparative substrate scanning mutagenesis studies revealed a unique pattern of crucial substrate residues for each subtype. Based upon structural coordinates of F1 bound to an inhibitor polypeptide, the mutational analyses suggest different substrate interactions in the substrate binding channel of each subtype. ; This research was funded by Deutsche Forschungsgemeinschaft, grant number Bi 660/3-1, to T.B., by Swiss Federal Department of Defence, Civil Protection and Sport, grant number 353003364/Stm, and by the Federal Ministry of Education and Research, grant number 031L0111A, TiViBoNT, to B.G.D. The APC was funded by Hannover Medical School, Hannover, Germany. ; Sí |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 2072-6651 |
| العلاقة: | Publisher's version; https://doi.org/10.3390/toxins10080311Test; info:eu_repo/grantAgreement/ES/ Bi 660/3-1; info:eu_repo/grantAgreement/ES/ 353003364/Stm; info:eu_repo/grantAgreement/ES/031L0111A; Toxins (Basel). 2018 Aug 1;10(8). pii: E311.; http://hdl.handle.net/20.500.12105/9796Test; Toxins |
| DOI: | 10.3390/toxins10080311 |
| الإتاحة: | https://doi.org/20.500.12105/9796Test https://doi.org/10.3390/toxins10080311Test https://hdl.handle.net/20.500.12105/9796Test |
| حقوق: | http://creativecommons.org/licenses/by/4.0Test/ ; Atribución 4.0 Internacional ; info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.D0A8AAC7 |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 20726651 |
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| DOI: | 10.3390/toxins10080311 |