IRES-mediated Pichia pastoris cell-free protein synthesis

Yanan Wang , Ting Wang , Xinjie Chen , Yuan Lu

Bioresources and Bioprocessing ›› 2023, Vol. 10 ›› Issue (1) : 35

PDF
Bioresources and Bioprocessing ›› 2023, Vol. 10 ›› Issue (1) : 35 DOI: 10.1186/s40643-023-00653-4
Research

IRES-mediated Pichia pastoris cell-free protein synthesis

Author information +
History +
PDF

Abstract

Cell-free protein synthesis (CFPS) system is an ideal platform for fast and convenient protein research and has been used for macromolecular assembly, unnatural amino acid embedding, glycoprotein production, and more. To realize the construction of an efficient eukaryotic CFPS platform with the advantages of low cost and short time, a CFPS system based on the yeast Pichia pastoris was built in this study. The internal ribosomal entry site (IRES) can independently initiate translation and thus promote protein synthesis. The Kozak sequences can facilitate translation initiation. Therefore, the screening of IRES and its combination with Kozak was performed, in which cricket paralysis virus (CRPV) exhibited as the best translation initiation element from 14 different IRESs. Furthermore, the system components and reaction environment were explored. The protein yield was nearly doubled by the addition of RNase inhibitor. The cell extract amount, energy regeneration system (phosphocreatine and phosphocreatine kinase), and metal ions (K+ and Mg2+) were optimized to achieve the best protein synthesis yield. This P. pastoris CFPS system can extend the eukaryotic CFPS platform, providing an enabling technology for fast prototyping design and functional protein synthesis.

Keywords

Pichia pastoris / Cell-free protein synthesis / In vitro transcription–translation / IRES

Cite this article

Download citation ▾
Yanan Wang, Ting Wang, Xinjie Chen, Yuan Lu. IRES-mediated Pichia pastoris cell-free protein synthesis. Bioresources and Bioprocessing, 2023, 10(1): 35 DOI:10.1186/s40643-023-00653-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Ahn J-H, Choi C-Y, Kim D-M. Effect of energy source on the efficiency of translational termination during cell-free protein synthesis. Biochem Biophys Res Commun, 2005, 337: 325-329.

[2]

Alfi A, Popov A, Kumar A, . Cell-free mutant analysis combined with structure prediction of a lasso peptide Biosynthetic protease B2. Acs Synth Biol, 2022, 11: 2022-2028.

[3]

Aw R, Spice AJ, Polizzi KM. Methods for expression of recombinant proteins using a Pichia pastoris cell-free system. Curr Protoc Protein Sci, 2020, 102: e115.

[4]

Buntru M, Hahnengress N, Croon A, et al (2022) Data_Sheet_1_Plant-Derived Cell-Free Biofactories for the Production of Secondary Metabolites.DOCX: Figshare.

[5]

Calhoun KA, Swartz JR. Grandi G. Energy systems for ATP regeneration in cell-free protein synthesis reactions. In Vitro Transcription and Translation Protocols, 2007, Totowa, NJ: Humana Press, 3-17.

[6]

Chiba CH, Knirsch MC, Azzoni AR, . Cell-free protein synthesis: advances on production process for biopharmaceuticals and immunobiological products. Biotechniques, 2021, 70: 126-133.

[7]

Das Gupta M, Flaskamp Y, Roentgen R, . ALiCE<sup>®</sup>: A versatile, high yielding and scalable eukaryotic cell-free protein synthesis (CFPS) system. bioRxiv, 2022

[8]

Dondapati SK, Stech M, Zemella A, . Cell-Free protein synthesis: a promising option for future drug development. BioDrugs, 2020, 34: 327-348.

[9]

Dresios J, Chappell SA, Zhou W, . An mRNA-rRNA base-pairing mechanism for translation initiation in eukaryotes. Nat Struct Mol Biol, 2006, 13: 30-34.

[10]

Gibson DG, Young L, Chuang RY, . Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat Methods, 2009, 6: 343-341.

[11]

Gregorio NE, Levine MZ, Oza JP. A user's guide to cell-free protein synthesis. Methods and Protocols, 2019

[12]

Heide C, Buldum G, Moya-Ramirez I, . Design, Development and Optimization of a Functional Mammalian Cell-Free Protein Synthesis Platform. Front Bioeng Biotechnol, 2021

[13]

Hou J, Chen X, Jiang N, . Toward efficient multiple-site incorporation of unnatural amino acids using cell-free translation system. Synth Syst Biotechnol, 2022, 7: 522-532.

[14]

Imamura M, Mori T, Takatsuki H, . Elucidation of the molecular basis of abnormal prion protein (PrP) formation in a cell-free system using baculovirus and Insect cell-derived recombinant PrP. Yakugaku Zasshi-J Pharm Soc Jpn, 2019, 139: 989-992.

[15]

Johnson RJ, McCoy JG, Bingman CA, . Inhibition of human pancreatic ribonuclease by the human ribonuclease inhibitor protein. J Mol Biol, 2007, 368: 434-449.

[16]

Juturu V, Wu JC. Heterologous protein expression in Pichia pastoris: latest research progress and applications. ChemBioChem, 2018, 19: 7-21.

[17]

Kanoi BN, Nagaoka H, Morita M, . Leveraging the wheat germ cell-free protein synthesis system to accelerate malaria vaccine development. Parasitol Int, 2021

[18]

Karbalaei M, Rezaee SA, Farsiani H. Pichia pastoris: a highly successful expression system for optimal synthesis of heterologous proteins. J Cell Physiol, 2020, 235: 5867-5881.

[19]

Kelwick R, Webb AJ, MacDonald JT, . Development of a Bacillussubtilis cell-free transcription-translation system for prototyping regulatory elements. Metab Eng, 2016, 38: 370-381.

[20]

Kim GW, Siddiqui A. N6-methyladenosine modification of HCV RNA genome regulates cap-independent IRES-mediated translation via YTHDC2 recognition. Proc Natl Acad Sci U S A, 2021

[21]

Kim YJ, Yu HH, Park YJ, . Anti-biofilm activity of cell-free supernatant of Saccharomyces Cerevisiae against Staphylococcus aureus. J Microbiol Biotechnol, 2020, 30: 1854-1861.

[22]

Li ZX, Li YT, Lin XM, . Supramolecular protein assembly in cell-free protein synthesis system. Bioresour Bioprocess, 2022

[23]

Lin SY, Wang YC, Hsiao CL. Prebiotic iron originates the peptidyl transfer origin. Mol Biol Evol, 2019, 36: 999-1007.

[24]

Marshall GR, Feng JA, Kuster DJ. Back to the future: ribonuclease a. Biopolymers, 2008, 90: 259-277.

[25]

Mezhyrova J, Mors K, Glaubitz C, . Fruitós EG, Giralt AA, . Applications of cell-free synthesized membrane protein precipitates. Methods in molecular biology (Clifton, NJ), 2022, New York, NY: Springer, US.

[26]

Olafsdóttir G, Svansson V, Ingvarsson S, . In vitro analysis of expression vectors for DNA vaccination of horses: the effect of a Kozak sequence. Acta Vet Scand, 2008, 50(1): 44.

[27]

Perez JG, Stark JC, Jewett MC. Cell-Free synthetic biology: engineering beyond the cell. Cold Spring Harb Perspect Biol, 2016

[28]

Pestova TV, Lomakin IB, Hellen CUT. Position of the CrPV IRES on the 40S subunit and factor dependence of IRES/80S ribosome assembly. EMBO Rep, 2004, 5: 906-913.

[29]

Rinnofner C, Felber M, Pichler H. Mapelli V, Bettiga M. Strains and molecular tools for recombinant protein production in Pichia pastoris. Methods in molecular biology (Clifton, NJ), 2022, New York, NY: Springer, US.

[30]

Smolskaya S, Logashina YA, Andreev YA. Escherichia coli extract-based cell-free expression system as an alternative for difficult-to-obtain protein biosynthesis. Int J Mol Sci, 2020

[31]

Takahashi K, Sato G, Doi N, . A relationship between NTP and cell extract concentration for cell-free protein expression. Life, 2021, 11: 237.

[32]

Thoring L, Dondapati SK, Stech M, . High-yield production of "difficult-to-express" proteins in a continuous exchange cell-free system based on CHO cell lysates. Sci Rep, 2017

[33]

Várnai A, Tang C, Bengtsson O, . Expression of endoglucanases in Pichia pastoris under control of the GAP promoter. Microb Cell Factories, 2014, 13: 57.

[34]

Vilkhovoy M, Adhikari A, Vadhin S, . The evolution of cell free biomanufacturing. Processes, 2020, 8: 675.

[35]

Wang S, Rong Y, Wang Y, . Homogeneous production and characterization of recombinant N-GlcNAc-protein in Pichia pastoris. Microb Cell Factories, 2020

[36]

Wang Y, Chen X, Gao W, . Mechanism investigation for efficient cell-free unnatural amino acid embedding. Process Biochem, 2022, 122: 306-314.

[37]

Yang Y, Wang ZF. IRES-mediated cap-independent translation, a path leading to hidden proteome. J Mol Cell Biol, 2019, 11: 911-919.

[38]

Yang ZL, Zhang ZS. Engineering strategies for enhanced production of protein and bio-products in Pichia pastoris: a review. Biotechnol Adv, 2018, 36: 182-195.

[39]

Yang Y, Fan XJ, Mao MW, . Extensive translation of circular RNAs driven by N-6-methyladenosine. Cell Res, 2017, 27: 626-641.

[40]

Zemella A, Thoring L, Hoffmeister C, . Cell-free protein synthesis: pros and cons of prokaryotic and eukaryotic systems. ChemBioChem, 2015, 16: 2420-2431.

[41]

Zhang LK, Liu WQ, Li J. Establishing a Eukaryotic Pichia pastoris cell-free protein synthesis system. Front Bioeng Biotechnol, 2020

[42]

Zheng X, Zhang Y, Zhang X, . Fhl1p protein, a positive transcription factor in Pichia pastoris, enhances the expression of recombinant proteins. Microb Cell Fact, 2019

Funding

National Natural Science Foundation of China(22278241)

National Key R&D Program of China(2018YFA0901700)

Institute Guo Qiang, Tsinghua University(2021GQG1016)

Department of Chemical Engineering-iBHE Joint Cooperation Fund

AI Summary AI Mindmap
PDF

194

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/