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MPD and DNA Bending in Crystals and in Solution
Affiliation:1. College of Chemistry, Xiangtan University, Xiangtan 411105, People''s Republic of China;2. School of Chemical Engineering, Xiangtan University, Xiangtan 411105, People''s Republic of China;3. Key Lab of Environment-friendly Chemistry and Application in Ministry of Education, Xiangtan University, Xiangtan 411105, People''s Republic of China;4. Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Xiangtan University, Xiangtan 411105, People''s Republic of China;1. College of Chemistry, Xiangtan University, Xiangtan 411105, People''s Republic of China;2. School of Chemical Engineering, Xiangtan University, Xiangtan 411105, People''s Republic of China;3. Key Lab of Environment-friendly Chemistry and Application in Ministry of Education, Xiangtan University, Xiangtan 411105, People''s Republic of China;1. FSBEI HE Rostov State Medical University of Ministry of Health of the Russian Federation, 29 Nakhichevansky st., Rostov-on-Don 344022, Russia;2. Chemical Faculty of Southern Federal University, 7 Zorge St., Rostov-on-Don 344090, Russia
Abstract:Bending of 15 to 24° is observed within crystal structures ofB-DNA duplexes, is strongly sequence-dependent, and exhibits no correlation with the concentration of MPD (2-methyl-2,4-pentanediol) in the crystallizing solution. Two types of bends are observed: facultative bends or flexible hinges at junctions between regions of G·C and A·T base-pairs, and a persistent and almost obligatory bend at the center of the sequence R-G-C-Y. Only A-tracts are characteristically straight and unbent in every crystal structure examined to date. A detailed examination of normal vector plots for individual strands of a double helix provides an explanation, in terms of the stacking properties of guanine and adenine bases. The effect of high MPD concentrations, in both solution and crystal, is to decrease local bending somewhat without removing it altogether. MPD gel retardation experiments provide no basis for choosing among the three models that seek to explain macroscopic curvature of DNA by means of microscopic bending: junction bending, bent A-tracts, or bent general- sequence DNA. Crystallographic data on the straightness of A-tracts, the bendability of non-A sequences, and the identity of inclination angles in A-tract and non-A-tractB-DNA support only the general-sequence bending model. The pre-melting transition observed in A-tract DNA probably represents a relaxation of stiff adenine stacks to a flexible conformation more typical of general-sequence DNA.
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