MIKESOVA, Jana, Daria MILIAIEVA, Pavla STENCLOVA, Marek KINDERMANN, Tereza VUCKOVA, Marcela MADLIKOVA, Milan FABRY, Vaclav VEVERKA, Jiri SCHIMER, Pavel KREJČÍ, Stepan STEHLIK and Petr CIGLER. Nanodiamonds as traps for fibroblast growth factors: Parameters influencing the interaction. Carbon. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD, 2022, vol. 195, No 15, p. 372-386. ISSN 0008-6223. Available from: https://dx.doi.org/10.1016/j.carbon.2022.04.017.
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Basic information
Original name Nanodiamonds as traps for fibroblast growth factors: Parameters influencing the interaction
Authors MIKESOVA, Jana (203 Czech Republic), Daria MILIAIEVA, Pavla STENCLOVA (203 Czech Republic), Marek KINDERMANN (203 Czech Republic), Tereza VUCKOVA (203 Czech Republic), Marcela MADLIKOVA (203 Czech Republic), Milan FABRY (203 Czech Republic), Vaclav VEVERKA (203 Czech Republic), Jiri SCHIMER (203 Czech Republic), Pavel KREJČÍ (203 Czech Republic, belonging to the institution), Stepan STEHLIK (203 Czech Republic) and Petr CIGLER (203 Czech Republic, guarantor).
Edition Carbon, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2022, 0008-6223.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10403 Physical chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 10.900
RIV identification code RIV/00216224:14110/22:00126271
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.carbon.2022.04.017
UT WoS 000831026300009
Keywords in English Nanodiamond; Fibroblast growth factor; Binding; Sequestration; Thermodynamics
Tags 14110513, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 16/1/2023 13:02.
Abstract
Fibroblast growth factors (FGFs) deliver external cell communication signals, to regulate mammalian development, metabolism and homeostasis. Blocking the FGF interactions with their receptors at the cell membrane is one of the promising strategies for treatment of diseases related to dysregulated FGF signaling, such as cancer, metabolic syndromes, and developmental disorders. Recently, detonation nanodiamonds (NDs) with positive ζ-potential were identified as highly effective and selective FGF binders, sequestering FGF molecules and preventing their interaction with receptors under physiological conditions, thus potentially eliminating the effect of FGF overexpression. Here, we investigated the influence of ND origin (detonation vs. high-pressure high-temperature), surface modification, size and separation/purification steps on the sequestration ability and binding affinity of FGF2, a representative member of the FGF family. We measured FTIR and Raman spectra of the NDs, assessed their colloidal behavior and ζ-potential, and correlated their properties with FGF2 interaction levels. Using Western blot and ELISA, we quantified the strength of the interaction between detonation NDs and FGF2. All NDs with positive ζ-potential sequestered FGF2 at its physiologically relevant concentrations. Hydrogenated detonation NDs showed the highest binding capacity. Using Langmuir model, we estimated the apparent dissociation constant between FGF2 and detonation ND with positive ζ-potential to be in the nanomolar range in full fetal bovine serum. Because such tight interaction between a protein and a solid nanoparticle occurred in ∼105-fold molar excess of serum proteins, we believe that NDs can potentially be used in vivo as selective FGF traps to regulate disorders caused by aberrant FGF signaling.
Links
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