Structures and properties of multi-stranded nucleic acids

被引:33
作者
Lane, AN
Jenkins, TC
机构
[1] Natl Inst Med Res, Div Mol Struct, Div Mol Struct, London NW7 1AA, England
[2] Univ Bradford, Yorkshire Canc Res Lab Drug Design, Canc Res Grp, Bradford BD7 1DP, W Yorkshire, England
关键词
D O I
10.2174/1385272013375157
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nucleic acids exist in a number of Structural states that may comprise one to four strands. Common features involve base-stacking and pairing of complementary bases via H-bonded interactions, although a wide variety of pairing motifs are found in higher-order structures. Another property is the marked flexibility of nucleic acids reflected in their solution behaviour, thermodynamic stability and interactions with proteins and small ligand molecules. The electrostatic properties of a nucleic acid and its ability to pack into high-order structure(s) are largely determined by the anionic phosphodiester backbone. This feature is particularly evident for triple-helical assemblies, where there is close proximity between phosphates and intrinsic thermodynamic stability is strongly influenced by ionic strength. Structural stabilisation of parallel triplexes can also be modulated by the presence of positive charge, achieved through either N3-protonation of cytosine bases or the deliberate incorporation of charged residues into the third strand. Salt effects are also pronounced in four-stranded structures such as the i-motif and G-tetraplex ("quadruplex") assemblies; indeed, different structures are produced for the latter depending on the nature of the associated cation. High-order nucleic acid structures are currently a focus of intense interest in antisense and antigene strategies toward novel chemotherapeutic agents. An understanding of both their structural details and solution properties is essential for a rational approach to DNA-targeted drug design.
引用
收藏
页码:845 / 869
页数:25
相关论文
共 194 条
[1]   BASE-BASE MISMATCHES - THERMODYNAMICS OF DOUBLE HELIX FORMATION FOR DCA3XA3G + DCT3YT3G (X, Y = A,C,G,T) [J].
ABOULELA, F ;
KOH, D ;
TINOCO, I ;
MARTIN, FH .
NUCLEIC ACIDS RESEARCH, 1985, 13 (13) :4811-4824
[2]   HUMAN TELOMERIC C-STRAND TETRAPLEXES [J].
AHMED, S ;
KINTANAR, A ;
HENDERSON, E .
NATURE STRUCTURAL BIOLOGY, 1994, 1 (02) :83-88
[3]   Ab initio study of stacking interactions in A- and B-DNA [J].
Alhambra, C ;
Luque, FJ ;
Gago, F ;
Orozco, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (19) :3846-3853
[4]   How accurately and precisely can RNA structure be determined by NMR? [J].
Allain, FHT ;
Varani, G .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 267 (02) :338-351
[5]   STRUCTURE OF THE P1 HELIX FROM GROUP-I SELF-SPLICING INTRONS [J].
ALLAIN, FHT ;
VARANI, G .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 250 (03) :333-353
[6]   Conformational and thermodynamic properties of parallel intramolecular triple helices containing a DNA, RNA, or 2′-OMeDNA third strand [J].
Asensio, JL ;
Carr, R ;
Brown, T ;
Lane, AN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (48) :11063-11070
[7]   Comparison of the solution structures of intramolecular DNA triple helices containing adjacent and non-adjacent CG•C+ triplets [J].
Asensio, JL ;
Brown, T ;
Lane, AN .
NUCLEIC ACIDS RESEARCH, 1998, 26 (16) :3677-3686
[8]   Thermodynamic, kinetic, and conformational properties of a parallel intermolecular DNA triplex containing 5′ and 3′ junctions [J].
Asensio, JL ;
Dosanjh, HS ;
Jenkins, TC ;
Lane, AN .
BIOCHEMISTRY, 1998, 37 (43) :15188-15198
[9]   Solution conformation of a parallel DNA triple helix with 5′ and 3′ triplex-duplex junctions [J].
Asensio, JL ;
Brown, T ;
Lane, AN .
STRUCTURE WITH FOLDING & DESIGN, 1999, 7 (01) :1-11
[10]   The contribution of cytosine protonation to the stability of parallel DNA triple helices [J].
Asensio, JL ;
Lane, AN ;
Dhesi, J ;
Bergqvist, S ;
Brown, T .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (05) :811-822