Pregled bibliografske jedinice broj: 1206230
Modification of protein synthesis and secretory pathway to improve surface display efficiency
Modification of protein synthesis and secretory pathway to improve surface display efficiency // FEBS Open Bio Supplement for The Biochemistry Global Summit Vol 12
Lisabon: FEBS Press, 2022. str. 256-256 doi:10.1002/2211-5463.13440 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 1206230 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Modification of protein synthesis and secretory
pathway to improve surface display efficiency
Autori
Martinić-Cezar, Tea ; Lozančić, Mateja ; Žunar, Bojan ; Teparić, Renata ; Mrša, Vladimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
FEBS Open Bio Supplement for The Biochemistry Global Summit Vol 12
/ - Lisabon : FEBS Press, 2022, 256-256
Skup
The Biochemistry Global Summit
Mjesto i datum
Lisabon, Portugal, 06.07.2022. - 14.07.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Yeast, Surface Display, ER, transcription/translation regulation, UPR, ERAD
Sažetak
Major disadvantages of protein surface display in yeasts as an alter-native to classical solid- surface immobilization techniques are low production, secretion, and binding capacity, or simply said low surface display efficiency of recombinant proteins. As several problems could lead to low display efficiency, we attempted to investigate how modification of different cellular processes involved in the production and secretion of proteins can affect and possibly enhance display efficiency. For this purpose, we tested the effects of mutations of genes involved in transcription and translation (deltagcn2, deltagc- n5, deltaopi1, deltarrp6) and mutations affecting properties of the endoplasmic reticulum (deltayop1). We also tested the effect of mutations of genes involved in unfolded protein response (UPR) and the endoplasmic reticulum- associated degradation (ERAD) pathways that are possibly activated due to stress conditions caused by increased protein production of overexpressed recombinant protein.To test the effect of these mutations we used two reporter systems previously developed in our laboratory. Both systems contain beta-lactamase fused with either Pir2 protein or with the GPI anchoring signal sequence of Ccw12. Results obtained by measuring the activity of surface-displayed beta-lactamase have shown that it was possible to increase surface display efficiency significantly by modifying processes involved in protein production and secretion in yeast cells.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija
POVEZANOST RADA
Projekti:
IP-2019-04-2891 - Biotehnološka primjena ugradnje heterolognih proteina u stanične stijenke kvasaca (PRODIS) (Mrša, Vladimir, HRZZ - 2019-04) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb
Profili:
Bojan Žunar
(autor)
Vladimir Mrša
(autor)
Tea Martinić-Cezar
(autor)
Renata Teparić
(autor)
Mateja Lozančić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE