2022
<i>De novo</i> developed protein binders mimicking Interferon lambda signaling
KOLAROVA, Lucie; Jiri ZAHRADNIK; Maros HULICIAK; Pavel MIKULECKY; Yoav PELEG et al.Základní údaje
Originální název
<i>De novo</i> developed protein binders mimicking Interferon lambda signaling
Autoři
KOLAROVA, Lucie; Jiri ZAHRADNIK; Maros HULICIAK; Pavel MIKULECKY; Yoav PELEG; Maya SHEMESH; Gideon SCHREIBER a Bohdan SCHNEIDER
Vydání
FEBS Journal, MALDEN, Blackwell, 2022, 1742-464X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.400
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:90127/22:00139239
Organizační jednotka
CIISB II
UT WoS
EID Scopus
Klíčová slova anglicky
cytokine signaling; cytokines; directed evolution; IFN-lambda; IL-29; interferon lambda; protein scaffolds; yeast display
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 29. 3. 2025 14:57, Mgr. Eva Dubská
Anotace
V originále
We hereby describe the process of design and selection of nonantibody protein binders mimicking cytokine signaling. We chose to mimic signaling of IFN-lambda 1, type 3 interferon (also known as IL-29) for its novelty and the importance of its biological functions. All four known interferons lambda signal through binding to the extracellular domains of IL-28 receptor 1 (IL-28R1) and IL-10 receptor 2 (IL-10R2). Our binders were therefore trained to bind both receptors simultaneously. The bifunctional binder molecules were developed by yeast display, a method of directed evolution. The signaling capacity of the bivalent binders was tested by measuring phosphorylation of the JAK/STAT signaling pathway and production of mRNA of six selected genes naturally induced by IFN- lambda 1 in human cell lines. The newly developed bivalent binders offer opportunities to study cytokine-related biological functions and modulation of the cell behavior by receptor activation on the cell surfaces alternative to the use of natural IFN-lambda.
Návaznosti
| 90127, velká výzkumná infrastruktura |
|