Skip to main content

Methods for Determining Activity and Specificity of DNA Binding and DNA Cleavage by Class II Restriction Endonucleases

  • Protocol
Nuclease Methods and Protocols

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 160))

Abstract

Restriction endonucleases coupled with DNA methyltransferases form the restriction-modification (RM) systems that occur ubiquitously among bacteria. They protect bacterial cells against bacteriophage infection by cleaving incoming foreign DNA highly specifically if it contains the recognition sequence. Cellular DNA is protected from cleavage by a specific methylation within the recognition sequence, which is introduced by the methyltransferase (for review, see refs. 1,2). Restriction endonucleases recognize palindromic recognition sites, 4–8 base pairs in length. These enzymes are indispensable tools for genetic engineering. The biology and biochemistry of type II restriction endonucleases has been reviewed recently (3,4) and will be summarized only briefly here. Type IIS restriction enzymes differ from type II enzymes in that they recognize an asymmetric recognition sequence (for review, see ref. 5). Monomeric in solution, these enzymes consist of a DNA recognition domain and a catalytic domain (6).

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

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Noyer-Weidner, M. and Trautner, T. A. (1993) Methylation of DNA in prokaryotes, in DNA Methylation: Molecular Biology and Biological Significance (Jost, J. P. and Saluz, H. P., eds.), Birkhauser Verlag, Basel, pp. 40–108.

    Google Scholar 

  2. Cheng, X. (1995) Structure and function of DNA methyltransferases. Annu. Rev. Biophys. Biomol. Struct. 24, 293–318.

    Article  PubMed  CAS  Google Scholar 

  3. Roberts, R. J. and Halford, S. E. (1993) Type II restriction enzymes, in Nucleases (Linn, S. M., Lloyd, R. S., and Roberts, R. J., eds.), Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, pp. 35–88.

    Google Scholar 

  4. Pingoud, A. and Jeltsch, A. (1997) Recognition and cleavage of DNA by type-II restriction endonucleases. Eur. J. Biochem. 246, 1–22.

    Article  PubMed  CAS  Google Scholar 

  5. Szybalski, W., Kim, S. C., Hasan, N., and Podhajska, A. J. (1991) Class-IIS restriction enzymes—a review. Gene 100, 13–26.

    Article  PubMed  CAS  Google Scholar 

  6. Li, L., Wu, L. P., and Chandrasegaran, S. (1992) Functional domains in FokI restriction endonuclease. Proc. Natl. Acad. Sci. USA 89, 4275–4279.

    Article  PubMed  CAS  Google Scholar 

  7. Alves, J., Urbanke, C., Fliess, A., Maass, G., and Pingoud, A. (1989) Fluorescence stopped-flow kinetics of the cleavage of synthetic oligodeoxynucleotides by the EcoRI restriction endonuclease. Biochemistry 28, 7879–7888.

    Article  PubMed  CAS  Google Scholar 

  8. Baldwin, G. S., Vipond, I. B., and Halford, S. E. (1995) Rapid reaction analysis of the catalytic cycle of the EcoRV restriction endonuclease. Biochemistry 34, 705–714.

    Article  PubMed  CAS  Google Scholar 

  9. Jack, W. E., Terry, B. J., and Modrich, P. (1982) Involvement of outside DNA sequences in the major kinetic path by which EcoRI endonuclease locates and leaves its recognition sequence. Proc. Natl. Acad. Sci. USA 79, 4010–4014.

    Article  PubMed  CAS  Google Scholar 

  10. Terry, B. J., Jack, W. E., and Modrich, P. (1985) Facilitated diffusion during catalysis by EcoRI endonuclease: nonspecific interactions in EcoRI catalysis. J. Biol. Chem. 260, 13,130–13,137.

    PubMed  CAS  Google Scholar 

  11. Ehbrecht, H.-J., Pingoud, A., Urbanke, C., Maass, G., and Gualerzi, C. (1985) Linear diffusion of restriction endonucleases on DNA. J. Biol. Chem. 260, 6160–6166.

    PubMed  CAS  Google Scholar 

  12. Jeltsch, A., Alves, J., Wolfes, H., Maass, G., and Pingoud, A. (1994) Pausing of the restriction endonuclease EcoRI during linear diffusion on DNA. Biochemistry 33, 10,215–10,219.

    Article  PubMed  CAS  Google Scholar 

  13. Jeltsch, A., Wenz, C., Stahl, F., and Pingoud, A. (1996) Linear diffusion of the restriction endonuclease EcoRV on DNA is essential for the in vivo function of the enzyme. EMBO J. 15, 5104–5111.

    PubMed  CAS  Google Scholar 

  14. Jeltsch, A. and Pingoud, A. (1998) Kinetic characterization of linear diffusion of the restriction endonuclease EcoRV on DNA. Biochemistry 37, 2160–2169.

    Article  PubMed  CAS  Google Scholar 

  15. Schulze, C., Jeltsch, A., Franke, I., Urbanke, C., and Pingoud, A. (1998) Crosslinking the EcoRV restriction endonuclease across the DNA-binding site reveals transient intermediates and conformational changes of the enzyme during DNA binding and catalytic turnover. EMBO J. 17, 6757–6766.

    Article  PubMed  CAS  Google Scholar 

  16. Kim, Y., Grable, J. C., Love, R., Greene, P. J., and Rosenberg, J. M. (1990) Refinement of EcoRI endonuclease crystal structure: a revised protein chain tracing. Science 249, 1307–1309.

    Article  PubMed  CAS  Google Scholar 

  17. Winkler, F. K., Banner, D. W., Oefner, C., Tsernoglou, D., Brown, R. S., Heathman, S. P., Bryan, R. K., Martin, P. D., Petratos, K., and Wilson, K. S. (1993) The crystal structure of EcoRV endonuclease and of its complexes with cognate and non-cognate DNA fragments. EMBO J. 12, 1781–1795.

    PubMed  CAS  Google Scholar 

  18. Athanasiadis, A., Vlassi, M., Kotsifaki, D., Tucker, P. A., Wilson, K. S., and Kokkinidis, M. (1994) Crystal structure of PvuII endonuclease reveals extensive structural homologies to EcoRV. Nat. Struct. Biol. 1, 469–475.

    Article  PubMed  CAS  Google Scholar 

  19. Cheng, X., Balendiran, K., Schildkraut, I., and Anderson, J. E. (1994) Structure of PvuII endonuclease with cognate DNA. EMBO J. 13, 3927–3935.

    PubMed  CAS  Google Scholar 

  20. Newman, M., Strzelecka, T., Dorner, L. F., Schildkraut, I., and Aggarwal, A. K. (1994) Structure of restriction endonuclease BamHI and its relationship to EcoRI. Nature 368, 660–664.

    Article  PubMed  CAS  Google Scholar 

  21. Newman, M., Strzelecka, T., Dorner, L. F., Schildkraut, I., and Aggarwal, A. K. (1995) Structure of BamHI endonuclease bound to DNA: partial folding and unfolding on DNA binding. Science 269, 656–663.

    Article  PubMed  CAS  Google Scholar 

  22. Bozic, D., Grazulis, S., Siksnys, V., and Huber, R. (1996) Crystal structure of Citrobacter freundii restriction endonuclease Cfr10I at 2.15 Å resolution. J. Mol. Biol. 255, 176–186.

    Article  PubMed  CAS  Google Scholar 

  23. Newman, M., Lunnen, K., Wilson, G., Greci, J., Schildkraut, I., and Phillips, S. E. V. (1998) Crystal structure of restriction endonuclease BglI bound to its interrupted DNA recognition sequence. EMBO J. 17, 5466–5476.

    Article  PubMed  CAS  Google Scholar 

  24. Venclovas, C., Timinskas, A., and Siksnys, V. (1994) Five-stranded beta-sheet sandwiched with two a-helices: a structural link between restriction endonucleases EcoRI and EcoRV. Proteins 20, 279–282.

    Article  PubMed  CAS  Google Scholar 

  25. Wah, D. A., Hirsch, J. A., Dorner, L. F., Schildkraut, I., and Aggarwal, A. K. (1997) Structure of the multimodular endonuclease FokI bound to DNA. Nature 388, 97–100.

    Article  PubMed  CAS  Google Scholar 

  26. Wah, D. A., Bitinaite, J., Schildkraut, I., and Aggarwal, A. K. (1998) Structure of FokI has implications for DNA cleavage. Proc. Natl. Acad. Sci. USA 95, 10,564–10,569.

    Article  PubMed  CAS  Google Scholar 

  27. Aggarwal, A. K. (1995) Structure and function of restriction endonucleases. Curr. Opin. Struct. Biol. 5, 11–19.

    Article  PubMed  CAS  Google Scholar 

  28. Rosenberg, J. M. (1991) Structure and function of restriction endonucleases. Curr. Opin. Struct. Biol. 1, 104–113.

    Article  CAS  Google Scholar 

  29. Lesser, D. R., Kurpiewski, M. R., and Jen-Jacobson, L. (1990) The energetic basis of specificity in the EcoRI endonuclease-DNA interaction. Science 250, 776–786.

    Article  PubMed  CAS  Google Scholar 

  30. Thielking, V., Alves, J., Fliess, A., Maass, G., and Pingoud, A. (1990) Accuracy of the EcoRI restriction endonuclease: Binding and cleavage studies with oligodeoxynucleotide substrates containing degenerate recognition sequences. Biochemistry 29, 4682–4691.

    Article  PubMed  CAS  Google Scholar 

  31. Alves, J., Selent, U., and Wolfes, H. (1995) Accuracy of the EcoRV restriction endonuclease: Binding and cleavage studies with oligodeoxynucleotide substrates containing degenerate recognition sequences. Biochemistry 34, 11,191–11,197.

    Article  PubMed  CAS  Google Scholar 

  32. Jeltsch, A., Alves, J., Oelgeschlager, T., Wolfes, H., Maass, G. M., and Pingoud, A. (1993) Mutational analysis of the function of Gln115 in the EcoRI restriction endonuclease, a critical amino acid for recognition of the inner thymidine residue in the sequence-GAATTC-and for coupling specific DNA binding to catalysis. J. Mol. Biol. 229, 221–234.

    Article  PubMed  CAS  Google Scholar 

  33. Stahl, F., Wende, W., Jeltsch, A., and Pingoud, A. (1996) Introduction of asymmetry in the naturally symmetric restriction endonuclease EcoRV to investigate intersubunit communication in the homodimeric protein. Proc. Natl. Acad. Sci. USA 93, 6175–6180.

    Article  PubMed  CAS  Google Scholar 

  34. Stahl, F., Wende, W., Jeltsch, A., and Pingoud, A. (1998) The mechanism of DNA cleavage by the type II restriction enzyme EcoRV: Asp36 is not directly involved in DNA cleavage but serves to couple indirect readout to catalysis. Biol. Chem. 379, 467–473.

    Article  PubMed  CAS  Google Scholar 

  35. Stahl, F., Wende, W., Wenz, C., Jeltsch, A., and Pingoud, A. (1998) Intra-vs intersubunit communication in the homodimeric restriction enzyme EcoRV: Thr37 and Lys38 involved in indirect readout are only important for the catalytic activity of their own subunit. Biochemistry 37, 5682–5688.

    Article  PubMed  CAS  Google Scholar 

  36. Smith, H. O. and Wilcox, K. W. (1970) A restriction enzyme from Haemophilus influenzae. I. Purification and general properties. J. Mol. Biol. 51, 379–391.

    Article  PubMed  CAS  Google Scholar 

  37. Connolly, B. A., Eckstein, F., and Pingoud, A. (1984) The Stereochemical course of the restriction endonuclease EcoRI-catalyzed reaction. J. Biol. Chem. 259, 10,760–10,763.

    PubMed  CAS  Google Scholar 

  38. Grasby, J. A. and Connolly, B. A. (1992) Stereochemical outcome of the hydrolysis reaction catalyzed by the EcoRV restriction endonuclease. Biochemistry 31, 7855–7861.

    Article  PubMed  CAS  Google Scholar 

  39. Jeltsch, A., Alves, J., Maass, G., and Pingoud, A. (1992) On the catalytic mechanism of EcoRI and EcoRV. A detailed proposal based on biochemical results, structural data and molecular modelling. FEBS Lett. 304, 4–8.

    Article  PubMed  CAS  Google Scholar 

  40. Thielking, V., Selent, U., Köhler, E., Wolfes, H., Pieper, U., Geiger, R., Urbanke, C., Winkler, F. K., and Pingoud, A. (1991) Site-directed mutagenesis studies with EcoRV restriction endonuclease to identify regions involved in recognition and catalysis. Biochemistry 30, 6416–6422.

    Article  PubMed  CAS  Google Scholar 

  41. Winkler, F. K. (1992) Structure and function of restriction endonucleases. Curr. Opin. Struct. Biol. 2, 93–99.

    Article  Google Scholar 

  42. Jeltsch, A., Alves, J., Wolfes, H., Maass, G., and Pingoud, A. (1993) Substrate-assisted catalysis in the cleavage of DNA by the EcoRI and EcoRV restriction enzymes. Proc. Natl. Acad. Sci. USA 90, 8499–8503.

    Article  PubMed  CAS  Google Scholar 

  43. Vipond, I. B., Baldwin, G. S., and Halford, S. E. (1995) Divalent metal ions at the active sites of the EcoRV and EcoRI restriction endonucleases. Biochemistry 34, 697–704.

    Article  PubMed  CAS  Google Scholar 

  44. Kostrewa, D. and Winkler, F. K. (1995) Mg2+ binding to the active site of EcoRV endonuclease: a crystallographic study of complexes with substrate and product DNA at 2 Angstrom resolution. Biochemistry 34, 683–696.

    Article  PubMed  CAS  Google Scholar 

  45. Riggs, A. D., Suzuki, H., and Bourgeois, S. (1970) Lac repressor-operator interaction. I. Equilibrium studies. J. Mol. Biol. 48, 67–83.

    Article  PubMed  CAS  Google Scholar 

  46. Riggs, A. D., Bourgeois, S., and Cohn, M. (1970) The lac repressor-operator interaction. 3. Kinetic studies. J. Mol. Biol. 53, 401–417.

    Article  PubMed  CAS  Google Scholar 

  47. Hinkle, D. C. and Chamberlin, M. J. (1972) Studies of the binding of Escherichia coli RNA polymerase to DNA. II. The kinetics of the binding reaction. J. Mol. Biol. 70, 187–195.

    Article  PubMed  CAS  Google Scholar 

  48. Hinkle, D. C. and Chamberlin, M. J. (1972) Studies of the binding of Escherichia coli RNA polymerase to DNA. I. The role of sigma subunit in site selection. J. Mol. Biol. 70, 157–185.

    Article  PubMed  CAS  Google Scholar 

  49. Wong, I. and Lohman, T. M. (1993) A double-filter method for nitrocellulose-filter binding: Application to protein-nucleic acid interactions. Proc. Natl. Acad. Sci. USA 90, 5428–5432.

    Article  PubMed  CAS  Google Scholar 

  50. Fried, M. and Crothers, D. M. (1981) Equilibria and kinetics of lac repressor-operator interactions by polyacrylamide gel electrophoresis. Nucleic Acids Res. 9, 6505–6525.

    Article  PubMed  CAS  Google Scholar 

  51. Garner, M. M. and Revzin, A. (1981) A gel electrophoresis method for quantifying the binding of proteins to specific DNA regions: application to components of the Escherichia coli lactose operon regulatory system. Nucleic Acids Res. 9, 3047–3060.

    Article  PubMed  CAS  Google Scholar 

  52. Stöver, T., Köhler, E., Fagin, U., Wende, W., Wolfes, H., and Pingoud, A. (1993) Determination of the DNA bend angle induced by the restriction endonuclease EcoRV in the presence of Mg2+. J. Biol. Chem. 268, 8645–8650.

    PubMed  Google Scholar 

  53. Withers, B. E. and Dunbar, J. C. (1993) The endonuclease isoschizomers, SmaI and XmaI bend DNA in opposite orientations. Nucleic Acids Res. 21, 2571–2577.

    Article  PubMed  CAS  Google Scholar 

  54. Vipond, I. B. and Halford, S. E. (1995) Specific DNA recognition by EcoRV restriction endonuclease induced by calcium ions. Biochemistry 34, 1113–1119.

    Article  PubMed  CAS  Google Scholar 

  55. Cal, S. and Connolly, B. A. (1996) The EcoRV modification methylase causes considerable bending of DNA upon binding to its recognition sequence GATATC. J. Biol. Chem. 271, 1008–1015.

    Article  PubMed  CAS  Google Scholar 

  56. Engler, L. E., Welch, K. K., and Jen-Jacobson, L. (1997) Specific binding by EcoRV endonuclease to its DNA recognition site GATATC. J. Mol. Biol. 269, 82–101.

    Article  PubMed  CAS  Google Scholar 

  57. Zhang, X., Duggan, L. J., and Gottlieb, P. A. (1993) Loading dyes used in gel electrophoresis alter the apparent thermodynamic equilibrium of the lac repressor-operator complex. Anal. Biochem 214, 580–582.

    Article  PubMed  CAS  Google Scholar 

  58. Hassanain, H. H., Dai, W., and Gupta, S. L. (1993) Enhanced gel mobility shift assay for DNA-binding factors. Anal. Biochem 213, 162–167.

    Article  PubMed  CAS  Google Scholar 

  59. Erskine, S. G. and Halford, S. E. (1998) Reactions of the EcoRV restriction endonuclease with fluorescent oligodeoxynucleotides: identical equilibrium constants for binding to specific and non-specific DNA. J. Mol. Biol. 275, 759–772.

    Article  PubMed  CAS  Google Scholar 

  60. Taylor, J. D., Badcoe, I. G., Clarke, A. R., and Halford, S. E. (1991) EcoRV restriction endonuclease binds all DNA sequences with equal affinity. Biochemistry 30, 8743–8753.

    Article  PubMed  CAS  Google Scholar 

  61. Thielking, V., Selent, U., Köhler, E., Landgraf, Z., Wolfes, H., Alves, J., and Pingoud, A. (1992) Mg2+ confers DNA binding specificity to the EcoRV restriction endonuclease. Biochemistry 31, 3727–3732.

    Article  PubMed  CAS  Google Scholar 

  62. Jeltsch, A., Maschke, H., Selent, U., Wenz, C., Köhler, E., Connolly, B. A., Thorogood, H., and Pingoud, A. (1995) DNA binding specificity of the EcoRV restriction endonuclease is increased by Mg2+ binding to a metal ion binding site distinct from the catalytic center of the enzyme. Biochemistry 34, 6239–6246.

    Article  PubMed  CAS  Google Scholar 

  63. Szczelkun, M. D. and Connolly, B. A. (1995) Sequence-specific binding of DNA by the EcoRV restriction and modification enzymes with nucleic acid and cofactor analogues. Biochemistry 34, 10,724–10,733.

    Article  PubMed  CAS  Google Scholar 

  64. Halford, S. E. and Goodall, A. J. (1988) Modes of DNA cleavage by the EcoRV restriction endonuclease. Biochemistry 27, 1771–1777.

    Article  PubMed  CAS  Google Scholar 

  65. Brownlee, G. G. and Sanger, F. (1969) Chromatography of 32P-labeled oligonucleotides on thin layers of DEAE-cellulose. Eur. J. Biochem. 11, 395–3999.

    Article  PubMed  CAS  Google Scholar 

  66. Fierke, C. A. and Hammes, G. G. (1995) Transient kinetic approaches to enzyme mechanisms. Methods Enzymol. 249, 3–37.

    Article  PubMed  CAS  Google Scholar 

  67. Johnson, K. A. (1995) Rapid quench kinetic analysis of polymerases, adenosinetri-phosphatases, and enzyme intermediates. Methods Enzymol. 249, 38–61.

    Article  PubMed  CAS  Google Scholar 

  68. Zebala, J., Choi, J., and Barany, F. (1992) Characterization of steady state, single-turnover, and binding kinetics of the TaqI restriction endonuclease. J. Biol. Chem. 267, 8097–8105.

    PubMed  CAS  Google Scholar 

  69. Groll, D. H., Jeltsch, A., Selent, U., and Pingoud, A. (1997) Does the restriction endonuclease EcoRV employ a two-metal-ion mechanism for DNA cleavage? Biochemistry 36, 11,389–11,401.

    Article  PubMed  CAS  Google Scholar 

  70. Erskine, S. G., Baldwin, G. S., and Halford, S. E. (1997) Rapid-reaction analysis of plasmid DNA cleavage by the EcoRV restriction endonuclease. Biochemistry 36, 7567–7576.

    Article  PubMed  CAS  Google Scholar 

  71. Jeltsch, A., Fritz, A., Alves, J., Wolfes, H., and Pingoud, A. (1993) A fast and accurate enzyme-linked immunosorbent assay for the determination of the DNA cleavage activity of restriction endonucleases. Anal. Biochem. 213, 234–240.

    Article  PubMed  CAS  Google Scholar 

  72. Wenz, C., Hahn, M., and Pingoud, A. (1998) Engineering of variants of the restriction endonuclease EcoRV that depend in their cleavage activity on the flexibility of sequences flanking the recognition site. Biochemistry 37, 2234–2242.

    Article  PubMed  CAS  Google Scholar 

  73. Glasner, W., Merkl, R., Schmidt, S., Cech, D., and Fritz, H. J. (1992) Fast quantitative assay of sequence-specific endonuclease activity based on DNA sequencer technology. Biol. Chem. Hoppe Seyler 373, 1223–1225.

    Article  PubMed  CAS  Google Scholar 

  74. van Holde, K. E., Johnson, W. C., and Ho, P. S. (1998) Principles of Physical Biochemistry. Prentice Hall, Upper Saddle River, NJ.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2001 Humana Press Inc.

About this protocol

Cite this protocol

Jeltsch, A., Pingoud, A.M. (2001). Methods for Determining Activity and Specificity of DNA Binding and DNA Cleavage by Class II Restriction Endonucleases. In: Schein, C.H. (eds) Nuclease Methods and Protocols. Methods in Molecular Biology™, vol 160. Humana Press. https://doi.org/10.1385/1-59259-233-3:287

Download citation

  • DOI: https://doi.org/10.1385/1-59259-233-3:287

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-679-6

  • Online ISBN: 978-1-59259-233-3

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics