Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Teodora Bavaro"'
Autor:
Roberta Bernardini, Sara Tengattini, Zhihao Li, Luciano Piubelli, Teodora Bavaro, Anamaria Bianca Modolea, Maurizio Mattei, Paola Conti, Stefano Marini, Yongmin Zhang, Loredano Pollegioni, Caterina Temporini, Marco Terreni
Publikováno v:
Biology Direct, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background To create a dual-acting vaccine that can fight against tuberculosis, we combined antigenic arabino-mannan analogues with the Ag85B protein. To start the process, we studied the impact of modifying different parts of the Ag85B prot
Externí odkaz:
https://doaj.org/article/e6875e639d254384814e86daf03d1955
Autor:
Marina S. Robescu, Teodora Bavaro, Fabrizio Medici, Giovanna Speranza, Daniela Ubiali, Marco Rabuffetti
Publikováno v:
Applied Sciences, Vol 14, Iss 14, p 6227 (2024)
5′-Phosphorylation of nucleosides is a reaction as important in nature and in industry as it is cumbersome to be performed. Whilst chemical phosphorylation relies on the use of harsh reagents, solvents, and conditions, as well as on the need for pr
Externí odkaz:
https://doaj.org/article/5d93e64059444213a9750ddce09128ef
Autor:
Marina S. Robescu, Sara Tengattini, Marco Rabuffetti, Giovanna Speranza, Marco Terreni, Teodora Bavaro
Publikováno v:
Catalysts, Vol 13, Iss 11, p 1399 (2023)
The β-d-mannopyranoside linkage is found in a number of biological structures, in particular, in the core trisaccharide of N-linked glycoproteins, as well as within the antigenic polysaccharides of Salmonella, yeasts, and glycolipids. The constructi
Externí odkaz:
https://doaj.org/article/5c724ac516dd49779808b2737eb9c5fc
Autor:
Sara Tengattini, Davide Rubes, Massimo Serra, Luciano Piubelli, Loredano Pollegioni, Enrica Calleri, Teodora Bavaro, Gabriella Massolini, Marco Terreni, Caterina Temporini
Publikováno v:
Pharmaceutics, Vol 15, Iss 5, p 1321 (2023)
Conjugation via disuccinimidyl homobifunctional linkers is reported in the literature as a convenient approach for the synthesis of glycoconjugate vaccines. However, the high tendency for hydrolysis of disuccinimidyl linkers hampers their extensive p
Externí odkaz:
https://doaj.org/article/fdd63fdbd081483e87674b5d09af04fb
Autor:
Teodora Bavaro, Sara Tengattini, Refaya Rezwan, Enrica Chiesa, Caterina Temporini, Rossella Dorati, Gabriella Massolini, Bice Conti, Daniela Ubiali, Marco Terreni
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Exogenous application of human epidermal growth factor (hEGF) stimulates epidermal wound healing. The aim of this study was to develop bioconjugates based on hEGF mimicking the protein in its native state and thus suitable for tissue enginee
Externí odkaz:
https://doaj.org/article/64b432ffe72c459892376f2d7e08c0ad
Autor:
Lisa Tanzi, Davide Rubes, Teodora Bavaro, Matthieu Sollogoub, Massimo Serra, Yongmin Zhang, Marco Terreni
Publikováno v:
Molecules, Vol 27, Iss 9, p 2776 (2022)
In the last few years, nanomaterials based on fullerene have begun to be considered promising tools in the development of efficient adjuvant/delivery systems for vaccination, thanks to their several advantages such as biocompatibility, size, and easy
Externí odkaz:
https://doaj.org/article/6b5e016c295c42688567fbc5143b1149
Autor:
Lisa Tanzi, Marina Simona Robescu, Sara Marzatico, Teresa Recca, Yongmin Zhang, Marco Terreni, Teodora Bavaro
Publikováno v:
Molecules, Vol 25, Iss 23, p 5764 (2020)
Regioselective deprotection of acetylated mannose-based mono- and disaccharides differently functionalized in anomeric position was achieved by enzymatic hydrolysis. Candida rugosa lipase (CRL) and Bacillus pumilus acetyl xylan esterase (AXE) were im
Externí odkaz:
https://doaj.org/article/2753f5e6fa4b41ffba58c1a4f94b236d
Autor:
Lucia Tamborini, Clelia Previtali, Francesca Annunziata, Teodora Bavaro, Marco Terreni, Enrica Calleri, Francesca Rinaldi, Andrea Pinto, Giovanna Speranza, Daniela Ubiali, Paola Conti
Publikováno v:
Molecules, Vol 25, Iss 5, p 1223 (2020)
The bi-enzymatic synthesis of the antiviral drug vidarabine (arabinosyladenine, ara-A), catalyzed by uridine phosphorylase from Clostridium perfringens (CpUP) and a purine nucleoside phosphorylase from Aeromonas hydrophila (AhPNP), was re-designed un
Externí odkaz:
https://doaj.org/article/e97f35237d29475e9ce57dd1e34048ed
Autor:
Francesca Tentori, Teodora Bavaro, Elisabetta Brenna, Danilo Colombo, Daniela Monti, Riccardo Semproli, Daniela Ubiali
Publikováno v:
Catalysts, Vol 10, Iss 2, p 260 (2020)
Ene-reductases (ERs) belonging to the old yellow enzyme (OYE) family have been thoroughly investigated for the stereospecific reduction of activated prochiral C=C double bonds. In this work, OYE3 was immobilized both by covalent binding on glyoxyl-ag
Externí odkaz:
https://doaj.org/article/315a6361a221490b9e0cd8469f762756
Publikováno v:
Catalysts, Vol 10, Iss 1, p 60 (2020)
We here described a three-step multi-enzymatic reaction for the one-pot synthesis of vidarabine 5′-monophosphate (araA-MP), an antiviral drug, using arabinosyluracil (araU), adenine (Ade), and adenosine triphosphate (ATP) as precursors. To this aim
Externí odkaz:
https://doaj.org/article/326c8147a0ab46e98c8dd361e2eeb75a