Amphiphilic DNA Duplex Stabilized by a Hydrophobic Zipper

被引:13
作者
Dohno, Chikara [1 ,2 ]
Shibata, Tomonori [1 ]
Okazaki, Masatsugu [1 ]
Makishi, Shingo [1 ]
Nakatani, Kazuhiko [1 ]
机构
[1] Osaka Univ, Dept Regulatory Bioorgan Chem, Inst Sci & Ind Res ISIR, Ibaraki 5670047, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
Bioorganic chemistry; Amphiphiles; DNA; Hydrophobic effect; MOLECULAR RECOGNITION; LIPID COMPLEX; OLIGONUCLEOTIDES; PHOSPHOTRIESTER; ASSEMBLIES; NUCLEOSIDE; BINDING;
D O I
10.1002/ejoc.201200540
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We have synthesized a new amphiphilic DNA containing an internal hydrophobic region consisting of dodecyl phosphotriester linkages (dod-DNA). dod-DNAs of any arbitrary sequence can be synthesized by standard automated solid-phase synthesis using a set of nucleoside dodecyl phosphoramidites. Although replacement of a phosphodiester linkage with the hydrophobic phosphotriester linkage tended to decrease the thermodynamic stability of the duplex, when multiple dodecyl groups were introduced into both strands of a DNA duplex in a face-to-face arrangement, the resulting duplex was strongly stabilized by the interstrand hydrophobic interaction. The hydrophobic zipper formation provides a tightly associated, electroneutral, and highly hydrophobic region in the originally hydrophilic DNA duplex. As the hydrophobic properties can be adjusted by varying the encoded sequence, dod-DNA is an easy-to-design amphiphilic molecule for controllable vesicles and membrane biotechnology.
引用
收藏
页码:5317 / 5323
页数:7
相关论文
共 36 条
[1]   HYDROPHOBIC EFFECTS ON SIMPLE ORGANIC-REACTIONS IN WATER [J].
BRESLOW, R .
ACCOUNTS OF CHEMICAL RESEARCH, 1991, 24 (06) :159-164
[2]   The ups and downs of nucleic acid duplex stability: structure-stability studies on chemically-modified DNA:RNA duplexes [J].
Freier, SM ;
Altmann, KH .
NUCLEIC ACIDS RESEARCH, 1997, 25 (22) :4429-4443
[3]   Nucleoside, nucleotide and oligonucleotide based amphiphiles:: a successful marriage of nucleic acids with lipids [J].
Gissot, Arnaud ;
Camplo, Michel ;
Grinstaff, Mark W. ;
Barthelemy, Philippe .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2008, 6 (08) :1324-1333
[4]   CRYSTAL-STRUCTURE OF THE HETERODIMERIC BZIP TRANSCRIPTION FACTOR C-FOS-C-JUN BOUND TO DNA [J].
GLOVER, JNM ;
HARRISON, SC .
NATURE, 1995, 373 (6511) :257-261
[5]   GENERAL-SYNTHESIS AND BINDING-AFFINITY OF POSITION-SELECTIVE PHOSPHONODIESTER-INCORPORATED AND PHOSPHOTRIESTER-INCORPORATED OLIGODEOXYRIBONUCLEOTIDES [J].
HAYAKAWA, Y ;
HIROSE, M ;
HAYAKAWA, M ;
NOYORI, R .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (04) :925-930
[6]   A DNA LIPID COMPLEX SOLUBLE IN ORGANIC-SOLVENTS [J].
IJIRO, K ;
OKAHATA, Y .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (18) :1339-1341
[7]   Stereocontrolled Solid-Phase Synthesis of Oligonucleoside H-Phosphonates by an Oxazaphospholidine Approach [J].
Iwamoto, Naoki ;
Oka, Natsuhisa ;
Sato, Terutoshi ;
Wada, Takeshi .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (03) :496-499
[8]   OLIGONUCLEOTIDE N-ALKYLPHOSPHORAMIDATES - SYNTHESIS AND BINDING TO POLYNUCLEOTIDES [J].
JAGER, A ;
LEVY, MJ ;
HECHT, SM .
BIOCHEMISTRY, 1988, 27 (19) :7237-7246
[9]   Preparation of supramolecular chromophoric assemblies using a DNA duplex [J].
Kashida, Hiromu ;
Asanuma, Hiroyuki .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (20) :7196-7204
[10]   Insulator Base Pairs for Lighting-up Perylenediimide in a DNA Duplex [J].
Kashida, Hiromu ;
Sekiguchi, Koji ;
Asanuma, Hiroyuki .
CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (38) :11554-11557