Literature DB >> 2828046

Influence of the protonation degree on the self-association properties of adenosine 5'-triphosphate (ATP).

R Tribolet1, H Sigel.   

Abstract

The concentration dependence of the chemical shifts for the protons H-2, H-8 and H-1' of ATP has been measured in D2O at 27 degrees C under several degrees of protonation in the pD range from 1.5 to 8.4. The results at pD greater than 4.5 are consistent with the isodesmic model of indefinite noncooperative stacking, while those at pD less than 4.5 indicate a preference for the formation of dimeric stacks. The stacking tendency follows the series, ATP4- (K = 1.3 M-1) less than D(ATP)3- (2.1 M-1) less than 1:1 ratio of D(ATP)3-/D2(ATP)-2- (6.0 M-1) much less than D2(ATP)2- (approximately 200 M-1) much greater than D3(ATP)- (K approximately less than 17 M-1) (for reasons of comparison all constants are expressed in the isodesmic model). These results are compared with previous data for adenosine [Ado (K = 15 M-1) greater than 1:1 ratio of Ado/D(Ado)+ (6.0 M-1) greater than D(Ado)+ (0.9 M-1)] and AMP [AMP2- (K = 2.1 M-1) less than D(AMP)- (3.4 M-1) less than 1:1 ratio of D(AMP)-/D2(AMP) +/- (5.6 M-1) greater than D2(AMP) +/- (approximately equal to 2 M-1) greater than D3(AMP)+ (K less than or equal to 1 M-1)] to facilitate the interpretation of the results for the ATP systems. Stack formation of H2(ATP)2- is clearly favored by additional ionic interactions; this is confirmed by measuring via potentiometric pH titrations the acidity constants of H2(ATP)2- in solutions containing different concentrations of ATP. It is suggested that in the [H2(ATP)]4-(2) dimer intermolecular ion pairs (and hydrogen bonds) are formed between the H+(N-1) site of one H2(ATP)2- and the gamma-P(OH)(O)-2 group of the other; in this way (a) the stack is further stabilized, and (b) the positive charges at the adenine residues are compensated (otherwise repulsion would occur as is evident from the adenosine systems). A detailed structure for the [H2(ATP)4-(2) dimer is proposed and some implications of the described stacking properties of ATP for biological systems are indicated.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2828046     DOI: 10.1111/j.1432-1033.1988.tb13742.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  5 in total

1.  Quantum and classical dynamics simulations of ATP hydrolysis in solution.

Authors:  Christopher B Harrison; Klaus Schulten
Journal:  J Chem Theory Comput       Date:  2012-05-21       Impact factor: 6.006

Review 2.  Coordination Chemistry of Nucleotides and Antivirally Active Acyclic Nucleoside Phosphonates, including Mechanistic Considerations.

Authors:  Astrid Sigel; Helmut Sigel; Roland K O Sigel
Journal:  Molecules       Date:  2022-04-19       Impact factor: 4.927

3.  Facilitated formation of high-molecular-weight associates of adenosine 5'-triphosphate (ATP).

Authors:  H Sigel; N A Corfù
Journal:  Naturwissenschaften       Date:  1995-05

Review 4.  Comparison of the π-stacking properties of purine versus pyrimidine residues. Some generalizations regarding selectivity.

Authors:  Astrid Sigel; Bert P Operschall; Helmut Sigel
Journal:  J Biol Inorg Chem       Date:  2014-01-25       Impact factor: 3.358

Review 5.  Self-association of nucleotides. Effects of protonation and metal ion coordination.

Authors:  H Sigel
Journal:  Biol Trace Elem Res       Date:  1989 Jul-Sep       Impact factor: 3.738

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.