scholarly journals Evaluation of the yeast surface display system for screening of functional nanobodies

AMB Express ◽  
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Kaho Kajiwara ◽  
Wataru Aoki ◽  
Mitsuyoshi Ueda
1998 ◽  
Vol 220 (1-2) ◽  
pp. 179-188 ◽  
Author(s):  
Bryan K. Cho ◽  
Michele C. Kieke ◽  
Eric T. Boder ◽  
K.Dane Wittrup ◽  
David M. Kranz

2020 ◽  
Vol 65 (6) ◽  
pp. 955-961
Author(s):  
Thu Pham Anh Nguyen ◽  
Thu Thi Minh Nguyen ◽  
Nghia Hieu Nguyen ◽  
Tri Nhan Nguyen ◽  
Thao Thi Phuong Dang

2020 ◽  
Vol 5 (4) ◽  
pp. 246-257
Author(s):  
SK Amir Hossain ◽  
SM Rifat Rahman ◽  
Toufiq Ahmed ◽  
Chanchal Mandal

Yeast surface display has become an increasingly popular tool for protein engineering and library screening applications. Although, recent advances have greatly expanded the capability of yeast surface display, the protein display system is still far away from industrial application. One of the major components of a stable, efficient and successful yeast surface display system is cell wall anchor protein with which our desired foreign protein will be attached. We studied 80 different yeast cell wall anchored proteins originated mostly from Saccharomyces cerevisiae and Candida albicans. We studied in details all the cell wall proteins in order to find out suitable cell wall proteins to recommend for the researchers to use in the construction of yeast display system. We considered selective physical properties of different yeast cell wall proteins that are crucial for selecting best suited cell surface anchor proteins which are molecular weight, binding domain of anchor protein, length of amino acid and fusion site. Finally, our studies showed that Ccw11, Ccw12. Cwp1, Cwp2, Dan1, Gas1, Gas5, Exg1, Ycr89, Ecm33, Pga4, Sap9, Sap10, Pst1, Pir1, Pir2, Pir3, Pir4, Cis1, Scw4, Scw6, Bgl2, Uth1, Scw1 are the promising and suitable cell wall anchor proteins could be used in construction of yeast cell surface display system. Additionally, this review presents detailed information about all the cell wall proteins in a single work. The future researchers in this field will be able to construct more efficient yeast display system for recombinant protein production at industrial scale using the knowledge presented in this work. Asian J. Med. Biol. Res. June 2019, 5(4): 246-257


2012 ◽  
Vol 512-515 ◽  
pp. 356-360 ◽  
Author(s):  
Ye Wang ◽  
Wen Qian Li ◽  
Xun Li ◽  
Hao Shi ◽  
Fei Wang

A Pichia pastoris cell-surface display system was constructed using a Flo1p anchor system containing N-terminal flocculation functional domain (874 residues, FS), derived from Saccharomyces cerevisiae. The lipase from Rhizopus oryzae with a pro sequence (ProROL) and green fluorescent protein (GFP) gene were successfully cloned and genetically fused to the anchor system with their C-terminus free. Fluorescence microscope was used to detect the GFP displayed on the recombinant P. pastoris cell surface. The results showed that the yeast surface display system using Flo1p as the anchor protein was successfully constructed, and the activity of ProROL displayed on KM71H reached to 217.15 U/g, much higher than 61.30 U/g reported by Matsumoto. Besides, the yeast surface display system could effectively shorten the fermentation time compared with traditional fermentation.


2014 ◽  
Vol 40 (12) ◽  
pp. 2081
Author(s):  
Hong CHEN ◽  
Hai-Xia NIU ◽  
Wen-Jing WANG ◽  
Hao-Ran MA ◽  
Jia-Na LI ◽  
...  

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