Volume 1, Issue 2 (Summer-Fall 2018)                   Mod Med Lab J 2018, 1(2): 84-90 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Omoumi N, Shokrgozar M, Noormohammadi Z. Design and Construction of Recombinant ELP-Intein Cassette for Use in Simple and new Purification Methods of Recombinant Proteins. Mod Med Lab J 2018; 1 (2) :84-90
URL: http://modernmedlab.com/article-1-43-en.html
Abstract:   (7502 Views)

Background and Objective: Use of elastin-like proteins (ELPs) provides high-performance protein purification without need for chromatography. In line with cost reduction and facilitation of recombinant proteins purification, which represent a high percentage of production costs, in this project, we eliminated the need for proteases in the process of separation of recombinant proteins from ELP by designing a cassette using ELPs properties as well as insertion of autocatalytic intein protein between the recombinant protein and ELP.
Methods: In this study, at first Mxe GyrA intein gene was amplified from pTXB1 vector by PCR method and cloned into pUC57-hEGF vector. Then, 8xELP repetitive sequences were first cloned in pUC57 vector and then into pUC57-intein-hEGF vector in the upstream of Intein-hEGF.
Result: The design and construction stages of pUC57-8xELP-Intein-hEGF cassette was successful and the accuracy of 8xELP-Intein-hEGF was confirmed by sequencing.
Conclusion: The use of ELP-intein cassette provides recombinant protein purification only with steps consisting of temperature, salt, and centrifugation, without need for proteolytic enzymes, and access to this technology provides the possibility of production and purification of recombinant proteins with minimum cost and facilities. 

Keywords: Purification, ELP, Intein
Full-Text [PDF 737 kb]   (3220 Downloads)    
Type of Study: Original Research Article | Subject: Laboratory Methods

References
1. Banki MR, Feng L, Wood DW. Simple bioseparations using self-cleaving elastin-like polypeptide tags. Nat Methods 2005;2(9):659-61. [DOI:10.1038/nmeth787] [PMID]
2. Chilkoti A, Dreher MR, Meyer DE. Design of thermally responsive, recombinant polypeptide carriers for targeted drug delivery. Adv Drug Deliv Rev 2002;54(8):1093-111. [DOI:10.1016/S0169-409X(02)00060-1]
3. Chong S, Mersha FB, Comb DG, Scott ME, Landry D, Vence LM, et al. Single-column purification of free recombinant proteins using a self-cleavable affinity tag derived from a protein splicing element. Gene 1997;192(2):271-81. [DOI:10.1016/S0378-1119(97)00105-4]
4. Cui C, Zhao W, Chen J, Wang J, Li Q. Elimination of in vivo cleavage between target protein and intein, in the intein-mediated protein purification. Protein Expr Purif 2006;50(1):74–81. [DOI:10.1016/j.pep.2006.05.019] [PMID]
5. LaVallie ER, McCoy JM, Gene fusion expression systems in Escherichia coli. Curr Opin Biotechnol 1995;6(5):501-6. [DOI:10.1016/0958-1669(95)80083-2]
6. Loughran ST, Loughran NB, Ryan BJ, D'Souza BN, Walls D.. Modified His-tag fusion vector for enhanced protein purification by immobilized metal affinity chromatography. Anal Biochem 2006; 355(1):148–50. [DOI:10.1016/j.ab.2006.05.011] [PMID]
7. Meyer D.E and Chilkoti A. Purification of recombinant proteins by fusion with thermally-responsive polypeptides. Nat Biotechnol 1999;17(11):1112-5. [DOI:10.1038/15100] [PMID]
8. Muralidharan V, Muir TW. Protein ligation an enabling technology for the biophysical analysis of proteins. Nat Methods 2006; 3(6):429–38. [DOI:10.1038/nmeth886] [PMID]
9. Sambrook J, Russell WD. Molecular Cloning: A Laboratory Manual. 3rd ed. New York: Cold Spring Harbor Laboratory Press; 2001; p. 441-542, 691-776.
10. Trabbic-Carlson K, Liu L, Kim B, Chilkoti A. Expression and purification of recombinant proteins from Escherichia coli: Comparison of an elastin-like polypeptide fusion with an oligohistidine fusion. Protein Sci 2004;13(12):3274-84. [DOI:10.1110/ps.04931604] [PMID] [PMCID]
11. Urry DW, Free energy transduction in polypeptides and proteins based on inverse temperature transitions. Prog Biophys Mol Biol 1992;57(1):23-57. [DOI:10.1016/0079-6107(92)90003-O]
12. Wood DW, Harcum SW, Belfort G. Industrial applications of intein technology. In: Belfort M, Derbyshire V, Stoddard BL, Wood DW, eds. Homing endonucleases and inteins, Berlin Heidelberg New York: Springer, vol. 16. 2005; p. 346-77. [DOI:10.1007/3-540-29474-0_20]
13. Xu M.Q and Evans T.C. Recent advances in protein splicing: manipulating proteins in vitro and in vivo. Curr Opin Biotechnol 2005;16(4):440-6. [DOI:10.1016/j.copbio.2005.06.012] [PMID]
14. Zakhartsev M, Momeu C. Purification of glucose oxidase from complex fermentation medium using tandem chromatography. J Chromatogr B Analyt Technol Biomed Life Sci 2007;858(1-2):151-8 [DOI:10.1016/j.jchromb.2007.08.015] [PMID]

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Modern Medical Laboratory Journal