Slow motion in the CAA center dot TTG sequence of a DNA decamer duplex studied by NMR

Citation
C. Kojima et al., Slow motion in the CAA center dot TTG sequence of a DNA decamer duplex studied by NMR, BIOCHEM, 40(24), 2001, pp. 7239-7246
Citations number
57
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMISTRY
ISSN journal
00062960 → ACNP
Volume
40
Issue
24
Year of publication
2001
Pages
7239 - 7246
Database
ISI
SICI code
0006-2960(20010619)40:24<7239:SMITCC>2.0.ZU;2-H
Abstract
In DNA duplexes, pyrimidine-purine steps are believed to be flexible or con formationally unstable. Indeed, several DNA crystal structures exhibit a mu ltitude of conformations for CpA . TpG steps. The question arises of whethe r this structural flexibility is accompanied by dynamical flexibility, i.e. , a question pertaining to the energy barrier between conformations. Except for TpA steps, slow motions on the microsecond-to-millisecond time scale h ave not been detected in duplexes until now. In the present study, such slo w motion was investigated by H-1, C-13, and N-15 NMR relaxation measurement s on a DNA decamer d(CATTTGCATC).d(GATGCAAATG). The DNA decamer was enriche d with 15% C-13 and 98% N-15 isotopes for each adenosine and guanosine resi due. Three lines of evidence support the notion of slow motion in the CAA . TTG moiety. Analysis of N-15 relaxation showed that the order parameter, S -2, of guanosine imino NH groups was about 0.8, similar to that of CH group s for this oligomer, The strong temperature dependence of guanosine NH S-2 in the CAA . TTG sequence indicated the presence of a large-amplitude motio n. Signals of adenosine H8 protons in the CAA . TTG sequence were broadened in 2D H-1 NOESY spectra, which also suggested the existence of slow motion . As well as being smaller than for other adenine residues, the H-1 T-2 val ues exhibited a magnetic field strength dependence for all adenosine H8 sig nals in the ATTTG . CAAAT region, suggesting slow motions more pronounced a t the first adenosine in the CAA . TTG sequence but extending over the CAAA T . ATTTG region. This phenomenon was further examined by the pulse field s trength dependence of the H-1, C-13, and N-15 T-1 rho values. H-1 and C-13 T-1 rho values showed a pulse field strength dependence, but N-15 T-1 rho d id not. Assuming a two-site exchange process, an exchange time constant of 20-300 mus was estimated for the first adenosine in the CAA sequence. The e xact nature of this motion remains unknown.