Biological activity and biotechnological aspects of peptide nucleic acid

被引:101
作者
Lundin, Karin E. [1 ]
Good, Liam [2 ]
Stromberg, Roger [3 ]
Graslund, Astrid [4 ]
Smith, C. I. Edvard [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Clin Res Ctr, Dept Lab Med, S-14186 Stockholm, Sweden
[2] Karolinska Inst, Ctr Genom & Bioinformat, S-17177 Stockholm, Sweden
[3] Karolinska Inst, Novum, Dept Biosci, S-14157 Huddinge, Sweden
[4] Stockholm Univ, Dept Biochem & Biophys, Arrhenius Lab, S-10691 Stockholm, Sweden
关键词
D O I
10.1016/S0065-2660(06)56001-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
During the latest decades a number of different nucleic acid analogs containing natural nucleobases on a modified backbone have been synthesized. An example of this is peptide nucleic acid (PNA), a DNA mimic with a noncyclic peptide-like backbone, which was first synthesized in 1991. Owing to its flexible and neutral backbone PNA displays very good hybridization properties also at low-ion concentrations and has subsequently attracted large interest both in biotechnology and biomedicine. Numerous modifications have been made, which could be of value for particular settings. However, the original PNA does so far perform well in many diverse applications. The high biostabitity makes it interesting for in vivo use, although the very limited diffusion over lipid membranes requires further modifications in order to make it suitable for treatment in eukaryotic cells. The possibility to use this nucleic acid analog for gene regulation and gene editing is discussed. Peptide nucleic acid is now also used for specific genetic detection in a number of diagnostic techniques, as well as for site-specific labeling and hybridization of functional molecules to both DNA and RNA, areas that are also discussed in this chapter. (c) 2006, Elsevier Inc.
引用
收藏
页码:1 / +
页数:53
相关论文
共 242 条
[11]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[12]  
Beck Frederik, 2002, Methods Mol Biol, V208, P29
[13]   Nuclear delivery of macromolecules: barriers and carriers [J].
Belting, M ;
Sandgren, S ;
Wittrup, A .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (04) :505-527
[14]   Combined triplex/duplex invasion of double-stranded DNA by "tail-clamp" peptide nucleic acid [J].
Bentin, T ;
Larsen, HJ ;
Nielsen, PE .
BIOCHEMISTRY, 2003, 42 (47) :13987-13995
[15]   Superior duplex DNA strand invasion by acridine conjugated peptide nucleic acids [J].
Bentin, T ;
Nielsen, PE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (21) :6378-6379
[16]   Enhanced peptide nucleic acid binding to supercoiled DNA: Possible implications for DNA ''breathing'' dynamics [J].
Bentin, T ;
Nielsen, PE .
BIOCHEMISTRY, 1996, 35 (27) :8863-8869
[17]  
Boffa LC, 2000, CANCER RES, V60, P2258
[18]   AN ASSESSMENT OF THE ANTISENSE PROPERTIES OF RNASE H-COMPETENT AND STERIC-BLOCKING OLIGOMERS [J].
BONHAM, MA ;
BROWN, S ;
BOYD, AL ;
BROWN, PH ;
BRUCKENSTEIN, DA ;
HANVEY, JC ;
THOMSON, SA ;
PIPE, A ;
HASSMAN, F ;
BISI, JE ;
FROEHLER, BC ;
MATTEUCCI, MD ;
WAGNER, RW ;
NOBLE, SA ;
BABISS, LE .
NUCLEIC ACIDS RESEARCH, 1995, 23 (07) :1197-1203
[19]   Resistance of decoy PNA-DNA chimeras to enzymatic degradation in cellular extracts and serum [J].
Borgatti, M ;
Romanelli, A ;
Saviano, M ;
Pedone, C ;
Lampronti, I ;
Breda, L ;
Nastruzzi, C ;
Bianchi, N ;
Mischiati, C ;
Gambari, R .
ONCOLOGY RESEARCH, 2003, 13 (05) :279-287
[20]   Transcription factor decoy molecules based on a peptide nucleic acid (PNA)-DNA chimera mimicking Sp1 binding sites [J].
Borgatti, M ;
Lampronti, I ;
Romanelli, A ;
Pedone, C ;
Saviano, M ;
Bianchi, N ;
Mischiati, C ;
Gambari, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :7500-7509