The interaction of amino acids, peptides, and proteins with DNA

被引:23
作者
Solovyev, Andrey Y. [1 ]
Tarnovskaya, Svetlana I. [2 ]
Chernova, Irina A. [1 ]
Shataeva, Larisa K. [1 ]
Skorik, Yury A. [1 ,3 ]
机构
[1] Russian Acad Sci, Inst Macromol Cpds, St Petersburg 199004, Russia
[2] St Petersburg State Polytech Univ, St Petersburg 195251, Russia
[3] St Petersburg State Chem Pharmaceut Acad, St Petersburg 197022, Russia
关键词
Amino acid; Regulatory peptide; Protein; DNA binding; Melting temperature; REGULATORY PEPTIDES; CALF THYMUS; BASE; POLYPEPTIDE; TRANSITIONS; COMPLEXES; CLUSTERS; BINDING;
D O I
10.1016/j.ijbiomac.2015.03.054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amino acids that carry charges on their side groups can bind to double stranded DNA (dsDNA) and change the strength of the double helix. Measurement of the DNA melting temperature (T-m) confirmed that acidic amino acids (Glu, Asp) weaken the H-bonds between DNA strands, whereas basic amino acids (Arg, Lys) strengthen the interaction between the strands. A rank correlation exists between the amino acid isoelectric points and the observed changes in T-m. A similar dependence of the hyperchromic effect on the isoelectric point of a protein (pepsin, insulin, cortexin, and protamine) was observed for DNA-protein complexes at room temperature. Short peptides (KE, AEDG, and KEDP) containing a mixture of acidic and basic amino acid residues also affect T-m and the stability of the double helix. A model for binding Gin and Lys to dsDNA was explored by a docking simulation. The model shows that Glu, in an untwisted shape, binds to dsDNA in its major groove and disrupts three H-bonds between the strands, thereby destabilizing the double helix. Lys, in an untwisted shape, binds to the external side of the dsDNA and forms two bonds with O atoms of neighboring phosphodiester groups, thereby strengthening the DNA helix. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
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