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Protein-DNA interactions: statistical analysis of interatomic contacts in major and minor grooves

https://doi.org/10.18699/VJ17.309

Abstract

The interactions between protein and DNA in essence underlie all processes in a living cell. Understanding the principles of specific recognition of DNA sites will open the way to understand how these processes are controlled and to interfere in their operation. In the paper we studied contacts between the protein and DNA at the atomic level in the structures of all the 3 518 protein­DNA complexes available in PDB by the Voronoi–Delaunay tessellation method. The method unambiguously defines contacts between atoms without any parameters, and characterizes each contact by the distance between atoms and the contact area, which is determined by the corresponding face of the Voronoi polyhedron. It was shown that most contacts are formed between the protein atoms and the sugarphosphate backbone of the DNA (72.9 %). The contact with the atoms of the nucleic bases emerging into the grooves of DNA is 17.0 % for a major groove and 10.1 % for all atomic contacts for a minor groove. Totally, the interaction between protein atoms and nucleic base atoms accounts for 27.1 % of all contacts. Analysis of the accessible surface area of atoms in the major and the minor grooves showed a correlation with the number of contacts (coefficient of linear correlation 0.94 and 0.93, respectively), however, nucleic acid atoms forming hydrogen bonds make contacts more often than may be expected from statistical considerations. It was shown that conformationally stable peptides occur sometimes in the binding regions with DNA. Analysis of the residues in a predefined conformation in 3 518 protein­DNA complexes revealed 159 amino acid residues in a predefined β­bend type I conformation, 15 residues in the conformation of β­bend type I’, and 6 residues in the conformation of β­bend type II. No residues in the conformation of β­bend type II’ were found. Analysis of contacts showed that such residues virtually do not form contacts with DNA. Contacts with nucleic base atoms are found only in the two homologous structures 3qea and 3qe9, where threonine atoms form contacts with atoms of nucleotide bases of the AT­pair.

About the Authors

A. A. Anashkina
Engelhardt Institute of Molecular Biology RAS.
Russian Federation
Moscow.


E. N. Kuznetsov
V.A. Trapeznikov Institute of Control Sciences RAS.
Russian Federation
Moscow.


A. V.  Batianovskii
Institute of Biophysics and Cell Engineering of NAS of Belarus.
Belarus
Minsk.


L. A. Uroshlev
Vavilov Institute of General Genetics RAS.
Russian Federation
Moscow.


V. G. Tumanyan
Engelhardt Institute of Molecular Biology RAS.
Russian Federation
Moscow.


N. G. Esipova
Engelhardt Institute of Molecular Biology RAS.
Russian Federation
Moscow.


References

1. Anashkina A.A., Kuznetsov E.N., Batyanovskii A.V., Gnuchev N.V., Tumanyan V.G., Esipova N.G. Classification of amino acids based on comparative analysis of contacts in DNA-protein complexes and specific DNA-protein interactions. Biophysics. 2013;58(6): 766-770.

2. Anashkina A.A., Kuznetsov E.N., Esipova N.G., Tumanyan V.G. Comprehensive statistical analysis of residues interaction specificity at protein – protein interfaces. Proteins: Struct. Funct. Bioinf. 2007; 67(4):1060-1077. DOI 10.1002/prot.21363.

3. Anashkina A.A., Tumanyan V.G., Kuznetsov E.N., Galkin A.V., Esipova N.G. Relative occurrence of amino acid-nucleotide contacts assessed by Voronoi–Delaunay tessellation of proteinDNA interfaces. Biophysics. 2008;53(3):199-201. DOI 10.1134/S0006350908030032.

4. Batyanovskii A.V., Esipova N.G., Shnoll S.E. Mutual disposition of short conformationally stanch oligopeptides in the 3D structure of globular proteins. Biophysics. 2009;54(6):748-752. DOI 10.1134/S0006350909060153.

5. Batyanovskii A.V., Vlasov P.K. Short protein segments with prevalent conformation. Biophysics. 2008;53(4):264-267. DOI 10.1134/S0006350908040040.

6. Benos P.V., Lapedes A.S., Stormo G.D. Is there a code for protein-DNA recognition? Probab(ilistical)ly… BioEssays. 2002;24(5):466-475. DOI 10.1002/bies.10073.

7. Choo Y., Klug A. Physical basis of a protein-DNA recognition code. Curr. Opin. Struct. Biol. 1997;7(1):117-125. DOI 10.1016/S0959440X(97)80015-2.

8. Corona R.I., Guo J.-T. Statistical analysis of structural determinants for protein-DNA-binding specificity. Proteins. 2016;84(8):1147-1161. DOI 10.1002/prot.25061.

9. Filippova G.N., Qi C.-F., Ulmer J.E., Moore J.M., Ward M.D., Hu Y.J., Loukinov D.I., Pugacheva E.M., Klenova E.M., Grundy P.E., Feinberg A.P., Cleton-Jansen A.M., Moerland E.W., Cornelisse C.J., Suzuki H., Komiya A., Lindblom A., Dorion-Bonnet F., Neiman P.E., Morse H.C., Collins S.J., Lobanenkov V.V. Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter its DNA-binding specificity. Cancer Res. 2002;62(1):48-52.

10. Luscombe N.M., Laskowski R.A., Thornton J.M. Amino acid–base interactions: a three-dimensional analysis of protein – DNA interactions at an atomic level. Nucleic Acids Res. 2001;29(13):2860-2874. DOI 10.1093/nar/29.13.2860.

11. Medvedev N.N. The algorithm for three-dimensional Voronoi polyhedra. J. Comput. Physics. 1986;67(1):223-229. DOI 10.1016/00219991(86)90123-3.

12. Pabo C.O., Nekludova L. Geometric analysis and comparison of protein-DNA interfaces: Why is there no simple code for recognition? J. Mol. Biol. 2000;301(3):597-624. DOI 10.1006/jmbi.2000.3918.

13. Privalov P.L. The state and role of water in biological systems. Biofizika = Biophysics. 1958;3(6):738-743. (in Russian)

14. Torshin I.Yu., Uroshlev L.A., Esipova N.G., Tumanyan V.G. Descriptive statistics of disallowed regions and various protein secondary structures in the context of studying twisted β-hairpins. Biophysics. 2016;61(1):6-12. DOI 10.1134/S0006350916010243.

15. Uroshlev L.A., Torshin I.Yu., Batyanovskii A.V., Esipova N.G., Tumanyan V.G. Disallowed conformations of a polypeptide chain as exemplified by the β-turn of the β-hairpin in the α-spectrin SH3 domain. Biophysics. 2015;60(1):1-9. DOI 10.1134/S0006350915010236.

16. Wolfe S.A., Nekludova L., Pabo C.O. DNA recognition by Cys2His2 zinc finger proteins. Annu. Rev. Biophys. Biomol. Struct. 2000;29: 183-212. DOI 10.1146/annurev.biophys.29.1.183.


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