Skip to main content
Log in

31P-NMR spectra of AP4

  • Original Papers
  • Published:
Research in Experimental Medicine

Summary

31P-NMR spectra were obtained from adenosine-5′-tetraphosphate under a variety of conditions and the four discernible resonances assigned. The pK-value of the metal-free compound was determined to be 6.4, the pK-value of the Mg2+ complex to be 5.3. The dissociation constant for the AP4⋅Mg2+ complex was estimated to be 10−4 M from the downfield shift of the resonances assigned to theγ- andδ-phosphorus nuclei. The binding of a second metal ion can also be followed by NMR; the dissociation constant for this ternary complex is several orders of magnitude larger than that for the binary complex.

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.

Similar content being viewed by others

References

  • Clonek T, Burt CT, Barany M (1981) NMR analysis of intact tissue including several examples of normal and diseased human muscle determinations. In: Damadian R (ed) NMR basic principles and progress, vol 19. NMR in medicine. Springer, Berlin Heidelberg New York, pp 121–159

    Google Scholar 

  • Feldhaus P, Froehlich T, Goody RS, Isakov M, Schirmer RH (1975) Synthetic inhibitors of adenylate kinases in the assay of ATPases and phosphokinases. Eur J Biochem 57:197–204

    PubMed  Google Scholar 

  • Gadian DG, Radda GK, Richards RE, Seeley PJ (1979)31-P NMR in living tissue: the road from a promising to an important tool in biochemistry. In: Shulman RG (ed) Biological applications of magnetic resonance. Academic Press, New York, pp 463–535

    Google Scholar 

  • Hoult DI, Busby SJW, Gadian DG, Radda GK, Richards RE, Seeley PJ (1974) Observation of tissue metabolites using31-P nuclear magnetic resonance. Nature 252:285–287

    PubMed  Google Scholar 

  • Jaffe E, Cohn M (1978)31-P Nuclear magnetic resonance spectra of the thiophosphate analogues of adenine nucleotides; effects of pH and Mg2+ binding. Biochemistry 17 [4]:652–657

    PubMed  Google Scholar 

  • Jardetzky O, Roberts GKC (1981) NMR in molecular biology. Academic Press, New York

    Google Scholar 

  • Keidel WD, Keidel J, Reiman V, Csatary N (1984) Study for clarifying two unknown peaks in the phosphorus magnetic resonance spectra appearing during the breakdown of high energy phosphates in ischemic heart and skeletal muscle. Res Exp Med 184:73–84

    Google Scholar 

  • Navon G, Shulman RG, Yamare T, Eccleshall TR, Lam KB, Baronofsky J, Marmur J (1978) “Phosphorus-31 nuclear magnetic resonance studies of wild-type and glycolytic pathway mutants ofSaccharomyces cerevisiae. Biochemistry 18:4487–4499

    Google Scholar 

  • Plateau P, Gueron M, Blanquet S (1981) Determination of dinucleoside 5′, 5‴-p1, P4-tetraphosphates by P31 and H1 NMR spectroscopy. Biochimie 63:837–830

    Google Scholar 

  • Son T-D, Roux M, Ellenberger M (1975) Interaction of Mg2+ ions with nucleoside triphosphates by phosphorus magnetic resonance spectroscopy. Nucleic Acids Res 2 [7]:1101–1110

    PubMed  Google Scholar 

  • Wuethrich K (1976) NMR in biological research: peptides and proteins. North-Holland, Amsterdam

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Klaus, W., Rösch, P. & Goody, R.S. 31P-NMR spectra of AP4 . Res. Exp. Med. 185, 145–150 (1985). https://doi.org/10.1007/BF01854900

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01854900

Key words

Navigation