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Naslov:In vitro functional validation of an anti-FREM2 nanobody for glioblastoma cell targeting
Avtorji:ID Krapež, Gloria (Avtor)
ID Šamec, Neja (Avtor)
ID Zottel, Alja (Avtor)
ID Katrašnik, Mojca (Avtor)
ID Kump, Ana (Avtor)
ID Šribar, Jernej (Avtor)
ID Križaj, Igor (Avtor)
ID Stojan, Jure (Avtor)
ID Romih, Rok (Avtor)
ID Bajc, Gregor (Avtor)
ID Butala, Matej (Avtor)
ID Muyldermans, Serge (Avtor)
ID Jovchevska, Ivana (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (23,98 MB)
MD5: FE32B13E77C5359E862E2F83D949ADC7
 
URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/2073-4468/14/1/8
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Background/Objectives: Glioblastomas are the most common brain malignancies. Despite the implementation of multimodal therapy, patient life expectancy after diagnosis is barely 12 to 18 months. Glioblastomas are highly heterogeneous at the genetic and epigenetic level and comprise multiple different cell subpopulations. Therefore, small molecules such as nanobodies, able to target membrane proteins specific to glioblastoma cells or specific cell types within the tumor are being investigated as novel tools to treat glioblastomas. Methods: Here, we describe the identification of such a nanobody and its in silico and in vitro validation. NB3F18, as we named it, is directed against the membrane-associated protein FREM2, overexpressed in glioblastoma stem cells. Results: Three dimensional in silico modeling indicated that NB3F18 and FREM2 form a stable complex. Surface plasmon resonance confirmed their interaction with moderate affinity. As we demonstrated by flow cytometry, NB3F18 binds to glioblastoma stem cells to a greater extent than to differentiated glioblastoma cells and astrocytes. Immunocytochemistry revealed surface localization of NB3F18 on glioblastoma stem cells, whereas cytoplasmic localization of NB3F18 was observed in other cell lines. NB3F18 was detected by transmission electron microscopy on the plasma membrane and in various compartments of the endocytic pathway, from endocytic vesicles to multivesicular bodies (endosomes) and lysosomes. Interestingly, NB3F18 was cytotoxic to glioblastoma stem cells. Conclusions: Collectively, NB3F18 has been qualified as an interesting tool to target glioblastoma cells and as a potential vehicle to deliver biological or pharmaceutical agents to these cells.
Ključne besede:brain cancer, membrane-bound protein, cytotoxicity, molecular tool, subcellular localization
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:str. 1-30
Številčenje:Vol. 14, iss. 1 [article no.] 8
PID:20.500.12556/DiRROS-28844 Novo okno
UDK:577.2
ISSN pri članku:2073-4468
DOI:10.3390/antib14010008 Novo okno
COBISS.SI-ID:225693187 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 10. 2. 2025;
Datum objave v DiRROS:09.04.2026
Število ogledov:188
Število prenosov:119
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Antibodies
Skrajšan naslov:Antibodies
Založnik:MDPI
ISSN:2073-4468
COBISS.SI-ID:3289339 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:Z3-1869-2019
Naslov:Razvoj anti-FREM2 nanotelesa in njegova uporaba pri ciljanju glioblastomskih celic.

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P1-0207-2020
Naslov:Toksini in biomembrane

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0108-2018
Naslov:Celična biologija in molekularna genetika v biomedicini

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P1-0390-2015
Naslov:Funkcijska genomika in biotehnologija za zdravje

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:I0- 0022
Naslov:Mreža raziskovalnih infrastrukturnih centrov Univerze v Ljubljani (MRIC UL)
Akronim:MRIC UL

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:možganski rak, membransko vezan protein, citotoksičnost, molekularno orodje, subcelična lokalizacija


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