VILÍM, Jan, Tereza GHAZALOVÁ, Eliška PETULOVÁ, Aneta HORACKOVA, Veronika STEPANKOVA, Radka CHALOUPKOVÁ, David BEDNÁŘ, Jiří DAMBORSKÝ and Zbyněk PROKOP. Computer-assisted stabilization of fibroblast growth factor FGF-18. Computational and Structural Biotechnology Journal. AMSTERDAM: Elsevier, 2023, vol. 21, October 2023, p. 5144-5152. ISSN 2001-0370. Available from: https://dx.doi.org/10.1016/j.csbj.2023.10.009.
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Basic information
Original name Computer-assisted stabilization of fibroblast growth factor FGF-18
Authors VILÍM, Jan (203 Czech Republic, belonging to the institution), Tereza GHAZALOVÁ (203 Czech Republic), Eliška PETULOVÁ (203 Czech Republic), Aneta HORACKOVA, Veronika STEPANKOVA, Radka CHALOUPKOVÁ (203 Czech Republic), David BEDNÁŘ (203 Czech Republic, belonging to the institution), Jiří DAMBORSKÝ (203 Czech Republic, guarantor, belonging to the institution) and Zbyněk PROKOP (203 Czech Republic, belonging to the institution).
Edition Computational and Structural Biotechnology Journal, AMSTERDAM, Elsevier, 2023, 2001-0370.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 6.000 in 2022
RIV identification code RIV/00216224:14310/23:00133177
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.csbj.2023.10.009
UT WoS 001097281900001
Keywords in English Computer-assisted stabilization; Fibroblast growth factor; Thermostability; Resistance to; Protease; Improved yield; FGF-18
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: prof. Mgr. Jiří Damborský, Dr., učo 1441. Changed: 30/1/2024 10:32.
Abstract
The fibroblast growth factors (FGF) family holds significant potential for addressing chronic diseases. Specifically, recombinant FGF18 shows promise in treating osteoarthritis by stimulating cartilage formation. However, recent phase 2 clinical trial results of sprifermin (recombinant FGF18) indicate insufficient efficacy. Leveraging our expertise in rational protein engineering, we conducted a study to enhance the stability of FGF18. As a result, we obtained a stabilized variant called FGF18-E4, which exhibited improved stability with 16 degrees C higher melting temperature, resistance to trypsin and a 2.5-fold increase in production yields. Moreover, the FGF18-E4 maintained mitogenic activity after 1-week incubation at 37 degrees C and 1-day at 50 degrees C. Additionally, the inserted mutations did not affect its binding to the fibroblast growth factor receptors, making FGF18-E4 a promising candidate for advancing FGF-based osteoarthritis treatment.
Links
EF18_053/0016952, research and development projectName: Postdoc2MUNI
FW03010208, research and development projectName: Stabilizace aplikačně atraktivních FGF proteinů pomocí pokročilých automatizovaných metod proteinového inženýrství
Investor: Technology Agency of the Czech Republic, Subprograms 1 Technology leaders
LM2018140, research and development projectName: e-Infrastruktura CZ (Acronym: e-INFRA CZ)
Investor: Ministry of Education, Youth and Sports of the CR
LM2023055, research and development projectName: Česká národní infrastruktura pro biologická data
Investor: Ministry of Education, Youth and Sports of the CR, ELIXIR-CZ: Czech National Infrastructure for Biological Data
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