Skip to main content

Advertisement

Log in

Efficient affinity-tagging of M13 phage capsid protein IX for immobilization of protein III-displayed oligopeptide probes on abiotic platforms

  • Applied genetics and molecular biotechnology
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

We developed a genetic approach to efficiently add an affinity tag to every copy of protein IX (pIX) of M13 filamentous bacteriophage in a population. Affinity-tagged phages can be immobilized on a surface in a uniform monolayer in order to position the pIII–displayed peptides or proteins for optimal interaction with ligands. The tagging consists of two major steps. First, gene IX (gIX) of M13 phage is mutated in Escherichia coli via genetic recombineering with the gIX::aacCI insertion allele. Second, a plasmid that co-produces the affinity-tagged pIX and native pVIII is transformed into the strain carrying the defective M13 gIX. This genetic complementation allows the formation of infective phage particles that carry a full complement (five copies per virion) of the affinity-tagged pIX. To demonstrate the efficacy of our method, we tagged a M13 derivative phage, M13KE, with Strep-tag II. In order to tag pIX with Strep-tag II, the phage genes for pIX and pVIII were cloned and expressed from pASG-IBA4 which contains the E. coli OmpA signal sequence and Strep-Tag II under control of the tetracycline promoter/operator system. We achieved the maximum phage production of 3 × 1011 pfu/ml when Strep-Tag II-pIX-pVIII fusion was induced with 10 ng/ml of anhydrotetracycline. The complete process of affinity tagging a phage probe takes less than 5 days and can be utilized to tag any M13 or fd pIII-displayed oligopeptide probes to improve their performance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Agrawal S, Kulabhusan PK, Joshi M, Bodas D, Paknikar KM (2016) A high affinity phage-displayed peptide as a recognition probe for the detection of Salmonella Typhimurium. J Biotechnol 231:40–45. https://doi.org/10.1016/j.jbiotec.2016.05.027

    Article  CAS  PubMed  Google Scholar 

  • Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (eds)(1993) Curr Prot Mol Biol. Greene Publishing Associates, Inc. and John Wiley & Sons, Inc.

  • Bertani G (1951) Studies on lysogenesis. I The mode of phage liberation by lysogenic Escherichia coli. J Bacteriol 62(3):293–300

    Article  CAS  Google Scholar 

  • Bishop-Hurley SL, Rea PJ, McSweeney CS (2010) Phage-displayed peptides selected for binding to Campylobacter jejuni are antimicrobial. Protein Eng Des Sel 23(10):751–757. https://doi.org/10.1093/protein/gzq050

    Article  CAS  PubMed  Google Scholar 

  • Brigati J, Williams DD, Sorokulova IB, Nanduri V, Chen IH, Turnbough CL Jr, Petrenko VA (2004) Diagnostic probes for Bacillus anthracis spores selected from a landscape phage library. Clin Chem 50(10):1899–1906

    Article  CAS  Google Scholar 

  • Chai Y, Li S, Horikawa S, Park MK, Vodyanoy V, Chin BA (2012) Rapid and sensitive detection of Salmonella Typhimurium on eggshells by using wireless biosensors. J Food Prot 75(4):631–636. https://doi.org/10.4315/0362-028x.jfp-11-339

    Article  PubMed  Google Scholar 

  • Chan S-W, Bye JM, Jackson P, Allain J-P (1996) Human recombinant antibodies specific for hepatitis C virus core and envelope E2 peptides from an immune phage display library. J Gen Virol 77(10):2531–2539. https://doi.org/10.1099/0022-1317-77-10-2531

    Article  CAS  PubMed  Google Scholar 

  • Chung WJ, Lee DY, Yoo SY (2014) Chemical modulation of M13 bacteriophage and its functional opportunities for nanomedicine. Int J Nanomedicine 9:5825–5836. https://doi.org/10.2147/IJN.S73883

    Article  PubMed  PubMed Central  Google Scholar 

  • Datsenko KA, Wanner BL (2000) One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A 97(12):6640–6645

    Article  CAS  Google Scholar 

  • Deng X, Wang L, You X, Dai P, Zeng Y (2018) Advances in the T7 phage display system (review). Mol Med Rep 17(1):714–720. https://doi.org/10.3892/mmr.2017.7994

    Article  CAS  PubMed  Google Scholar 

  • Hanahan D (1983) Studies on transformation of Escherichia coli with plasmids. J Mol Biol 166(4):557–580

    Article  CAS  Google Scholar 

  • Houbiers MC, Spruijt RB, Demel RA, Hemminga MA, Wolfs CJ (2001) Spontaneous insertion of gene 9 minor coat protein of bacteriophage M13 in model membranes. Biochim Biophys Acta 1511(2):309–316

    Article  CAS  Google Scholar 

  • Huang S, Li SQ, Yang H, Johnson ML, Wan J, Chen I, Petrenko VA, Barbaree JM, Chin BA (2008) Optimization of phage-based magnetoelastic biosensor performance. Sensor Trans J on Microsyst: Technol Appl 3:87–96

    CAS  Google Scholar 

  • Huang S, Yang H, Lakshmanan RS, Johnson ML, Wan J, Chen IH, Wikle HC 3rd, Petrenko VA, Barbaree JM, Chin BA (2009) Sequential detection of Salmonella typhimurium and Bacillus anthracis spores using magnetoelastic biosensors. Biosens Bioelectron 24(6):1730–1736. https://doi.org/10.1016/j.bios.2008.09.006

    Article  CAS  PubMed  Google Scholar 

  • Lakshmanan RS, Guntupalli R, Hu J, Kim DJ, Petrenko VA, Barbaree JM, Chin BA (2007) Phage immobilized magnetoelastic sensor for the detection of Salmonella typhimurium. J Microbiol Methods 71(1):55–60. https://doi.org/10.1016/j.mimet.2007.07.012

    Article  CAS  PubMed  Google Scholar 

  • Li SQ, Johnson ML, Wan J, Petrenko VA, Chin BA (2008) Microfabricated magnetoelastic biosensors for the detection of Bacillus anthracis spores. ECS Trans 16:177–185

    Article  CAS  Google Scholar 

  • Loset GA, Roos N, Bogen B, Sandlie I (2011) Expanding the versatility of phage display II: improved affinity selection of folded domains on protein VII and IX of the filamentous phage. PLoS One 6(2):e17433. https://doi.org/10.1371/journal.pone.0017433

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lu X, Weiss P, Block T (2004) A phage with high affinity for hepatitis B surface antigen for the detection of HBsAg. J Virol Methods 119(1):51–54

    Article  CAS  Google Scholar 

  • Martinez E, Bartolome B, de la Cruz F (1988) pACYC184-derived cloning vectors containing the multiple cloning site and lacZ alpha reporter gene of pUC8/9 and pUC18/19 plasmids. Gene 68(1):159–162

    Article  CAS  Google Scholar 

  • Mechaly A, Zahavy E, Fisher M (2008) Development and implementation of a single-chain Fv antibody for specific detection of Bacillus anthracis spores. Appl Environ Microbiol 74(3):818–822. https://doi.org/10.1128/aem.01244-07

    Article  CAS  PubMed  Google Scholar 

  • Mimmi S, Maisano D, Quinto I, Iaccino E (2019) Phage display: an overview in context to drug discovery. Trends Pharmacol Sci 40(2):87–91. https://doi.org/10.1016/j.tips.2018.12.005

    Article  CAS  PubMed  Google Scholar 

  • Moon JS, Choi EJ, Jeong NN, Sohn JR, Han DW, Oh JW (2019) Research progress of M13 bacteriophage-based biosensors. Nanomaterials (Basel) 9(10). https://doi.org/10.3390/nano9101448

    Article  CAS  Google Scholar 

  • Muzard J, Platt M, Lee GU (2012) M13 bacteriophage-activated superparamagnetic beads for affinity separation. Small 8(15):2403–2411. https://doi.org/10.1002/smll.201200099

    Article  CAS  PubMed  Google Scholar 

  • Nam KT, Peelle BR, Lee SW, Belcher AM (2004) Genetically driven assembly of nanorings based on the M13 virus. Nano Lett 4(1):23–27. https://doi.org/10.1021/nl0347536

    Article  CAS  Google Scholar 

  • Nanduri V, Bhunia AK, Tu S-I, Paoli GC, Brewster JD (2007) SPR biosensor for the detection of L. monocytogenes using phage-displayed antibody. Biosens Bioelectron 23(2):248–252

    Article  CAS  Google Scholar 

  • Niyomdecha S, Limbut W, Numnuam A, Kanatharana P, Charlermroj R, Karoonuthaisiri N, Thavarungkul P (2018) Phage-based capacitive biosensor for Salmonella detection. Talanta 188:658–664. https://doi.org/10.1016/j.talanta.2018.06.033

    Article  CAS  PubMed  Google Scholar 

  • Olsen EV, Sorokulova IB, Petrenko VA, Chen IH, Barbaree JM, Vodyanoy VJ (2006) Affinity-selected filamentous bacteriophage as a probe for acoustic wave biodetectors of Salmonella typhimurium. Biosens Bioelectron 21(8):1434–1442

    Article  CAS  Google Scholar 

  • Park M-K, Wikle HC, Chai Y, Horikawa S, Shen W, Chin BA (2012) The effect of incubation time for Salmonella Typhimurium binding to phage-based magnetoelastic biosensors. Food Control 26:539–545

    Article  Google Scholar 

  • Park M-K, Li S, Chin BA (2013a) Detection of Salmonella typhimurium grown directly on tomato surface using phage-based magnetoelastic biosensors. Food Bioprocess Technol 6:682–689

    Article  CAS  Google Scholar 

  • Park M-K, Park JH, Wikle HC 3rd, Chin BA (2013b) Evaluation of phage-based magnetoelastic biosensors for direct detection of Salmonella Typhimurium on spinach leaves. Sensors Actuators B Chem 176:1134–1140

    Article  CAS  Google Scholar 

  • Petrenko VA (2008) Landscape phage as a molecular recognition interface for detection devices. Microelectron J 39(2):202–207. https://doi.org/10.1016/j.mejo.2006.11.007

    Article  CAS  Google Scholar 

  • Petrenko VA, Smith GP, Gong X, Quinn T (1996) A library of organic landscapes on filamentous phage. Protein Eng 9:797–801

    Article  CAS  Google Scholar 

  • Rahbarnia L, Farajnia S, Babaei H, Majidi J, Veisi K, Ahmadzadeh V, Akbari B (2017) Evolution of phage display technology: from discovery to application. J Drug Target 25(3):216–224. https://doi.org/10.1080/1061186X.2016.1258570

    Article  CAS  PubMed  Google Scholar 

  • Ramji S, Lakshmanan RS, Guntupalli R, Petrenko VA, Chin BA (2007a) Phage based magnetoelastic sensor for the detection of Salmonella typhimurium. J Microbiol Methods 71(1):55–60

    Article  Google Scholar 

  • Ramji S, Lakshmanan RS, Hu J, Petrenko VA, Barbaree JM, Chin BA (2007b) Detection of Salmonella typhimurium in fat free milk using a phage immobilized magnetoelastic sensor. Sensors Actuators B 126(2):544–550

    Article  Google Scholar 

  • Sawada T, Serizawa T (2018) Filamentous viruses as building blocks for hierarchical self-assembly toward functional soft materials. Bull Chem Soc Jpn 91(3):455–466. https://doi.org/10.1246/bcsj.20170428

    Article  CAS  Google Scholar 

  • Schmidt TG, Koepke J, Frank R, Skerra A (1996) Molecular interaction between the strep-tag affinity peptide and its cognate target, streptavidin. J Mol Biol 255(5):753–766. https://doi.org/10.1006/jmbi.1996.0061

    Article  CAS  PubMed  Google Scholar 

  • Schweizer HP (1993) Small broad-host-range gentamycin resistance gene cassettes for site-specific insertion and deletion mutagenesis. Biotechniques 15(5):831–834

    CAS  PubMed  Google Scholar 

  • Shen W, Lakshmanan RS, Mathison LC, Petrenko VA, Chin BA (2009) Phage coated magnetoelastic micro-biosensors for real-time detection of Bacillus anthracis spores. Sensors Actuators B Chem 137:501–506

    Article  CAS  Google Scholar 

  • Smith GP (1985) Filamentous phage fusion: novel expression vectors that display cloned antigens on the surface of the viron. Science 228:1315–1317

    Article  CAS  Google Scholar 

  • Sorokulova IB, Olsen EV, Chen IH, Fiebor B, Barbaree JM, Vodyanoy VJ, Chin BA, Petrenko VA (2005) Landscape phage probes for Salmonella typhimurium. J Microbiol Methods 63(1):55–72

    Article  CAS  Google Scholar 

  • Tan WS, Tan GH, Yusoff K, Seow HF (2005) A phage-displayed cyclic peptide that interacts tightly with the immunodominant region of hepatitis B surface antigen. J Clin Virol 34(1):35–41

    Article  CAS  Google Scholar 

  • Tan Y, Tian T, Liu W, Zhu Z, C JY (2016) Advance in phage display technology for bioanalysis. Biotechnol J 11(6):732–745. https://doi.org/10.1002/biot.201500458

    Article  CAS  PubMed  Google Scholar 

  • Turnbough CL Jr (2003) Discovery of phage display peptide ligands for species-specific detection of Bacillus spores. J Microbiol Methods 53(2):263–271

    Article  CAS  Google Scholar 

  • Wan J, Shu H, Huang S, Fiebor B, Chen IH, Petrenko VA, Chin BA (2007a) Phage-based magnetoelastic wireless biosensors for detecting Bacillus anthracis spores. IEEE Sensors J 7(3):470–477

    Article  Google Scholar 

  • Wan JH, Johnson ML, Guntupalli VA, Petrenko VA, Chin BA (2007b) Detection of Bacillus anthracis spores in liquid using phage-based magnetoelastic micro-resonators. Sensors Actuators B Chem 127(2):559–566

    Article  CAS  Google Scholar 

  • Wu CH, Liu IJ, Lu RM, Wu HC (2016) Advancement and applications of peptide phage display technology in biomedical science. J Biomed Sci 23:8. https://doi.org/10.1186/s12929-016-0223-x

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

This research was partially supported by the United States Department of Agriculture National Institute of Food and Agriculture grant USDA-2016-67,021-25,005 and Alabama Agricultural Experimental Station Hatch grant ALA0SUH to Suh and Chin. Zhou Tong was supported by the Chinese Scholarship Council fellowship. Anwar Kalalah was supported by a scholarship from the Kingdom of Saudi Arabia.

Author information

Authors and Affiliations

Authors

Contributions

Zhou Tong, Laura Silo-Suh, Anwar Kalalah, and Paul Dawson performed the experiments. Bryan Chin and Sang-Jin Suh conceived and designed the study. Laura Silo-Suh and Sang-Jin Suh analyzed the data and supervised the project. Zhou Tong wrote the initial draft of the paper, and Laura Silo-Suh and Sang-Jin Suh revised the manuscript. All authors reviewed the manuscript.

Corresponding author

Correspondence to Sang-Jin Suh.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tong, Z., Silo-Suh, L.A., Kalalah, A. et al. Efficient affinity-tagging of M13 phage capsid protein IX for immobilization of protein III-displayed oligopeptide probes on abiotic platforms. Appl Microbiol Biotechnol 104, 1201–1209 (2020). https://doi.org/10.1007/s00253-019-10338-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-019-10338-8

Keywords

Navigation