Advances in SELEX and application of aptamers in the central nervous system

被引:70
作者
Yang, Yan [2 ]
Yang, Dongliang [2 ]
Schluesener, Hermann J. [1 ]
Zhang, Zhiren [1 ]
机构
[1] Univ Tubingen, Inst Brain Res, D-72076 Tubingen, Germany
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Ctr Med Expt, Wuhan 430030, Peoples R China
来源
BIOMOLECULAR ENGINEERING | 2007年 / 24卷 / 06期
基金
中国国家自然科学基金;
关键词
SELEX; aptamers; central nervous system;
D O I
10.1016/j.bioeng.2007.06.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
SELEX (Systematic Evolution of Ligands by Exponential Enrichment) is a screening technique that involves the progressive selection of highly specific ligands by repeated rounds of partition and amplification from a large combinatorial nucleic acid library. The products of the selection are called aptamers, which are short single stranded DNA or RNA molecules, binding with high affinity, attributed to their specific three-dimensional shapes, to a large variety of targets, ranging from small molecules to complex mixtures. Various improvement of the original SELEX method described in 1990 have been obtained recently, such as capillary electrophoresis SELEX, Toggle-SELEX, Tailored-SELEX, Photo-SELEX, and others. These new variants greatly shorten time of selection and improve aptamer affinity and specificity. Such aptamers have great potential as detecting and/or diagnostic reagents. Furthermore, some aptamers specifically inhibit biological functions of targeted proteins, and are considered as potent therapeutic lead structures evaluated in preclinical disease models. Recently, one aptamer has been approved by Food and Drug Administration of US for treating age-related macular degeneration. This review presents recent advances in the field of SELEX with special emphasis on applications of aptamers as analytical, diagnostic and therapeutic tools in the central nervous system. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:583 / 592
页数:10
相关论文
共 66 条
[51]   Structural determinants of conformationally selective, prion-binding aptamers [J].
Sayer, NM ;
Cubin, M ;
Rhie, A ;
Bullock, M ;
Tahiri-Alaoui, A ;
James, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :13102-13109
[52]   RNA aptamers as pathway-specific MAP kinase inhibitors [J].
Seiwert, SD ;
Nahreini, TS ;
Aigner, S ;
Ahn, NG ;
Uhlenbeck, OC .
CHEMISTRY & BIOLOGY, 2000, 7 (11) :833-843
[53]   Characterization and application of a novel RNA aptamer against the mouse prion protein [J].
Sekiya, S ;
Noda, K ;
Nishikawa, F ;
Yokoyama, T ;
Kumar, PKR ;
Nishikawa, S .
JOURNAL OF BIOCHEMISTRY, 2006, 139 (03) :383-390
[54]  
Seo HS, 2000, J MICROBIOL BIOTECHN, V10, P707
[55]   Modular aptameric sensors [J].
Stojanovic, MN ;
Kolpashchikov, DM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (30) :9266-9270
[56]  
Takemura K, 2006, EXP BIOL MED, V231, P204
[57]   Structures of MLSBK antibiotics bound to mutated large ribosomal subunits provide a structural explanation for resistance [J].
Tu, D ;
Blaha, G ;
Moore, PB ;
Steitz, TA .
CELL, 2005, 121 (02) :257-270
[58]   SYSTEMATIC EVOLUTION OF LIGANDS BY EXPONENTIAL ENRICHMENT - RNA LIGANDS TO BACTERIOPHAGE-T4 DNA-POLYMERASE [J].
TUERK, C ;
GOLD, L .
SCIENCE, 1990, 249 (4968) :505-510
[59]   In vitro selection of RNA molecules that displace cocaine from the membrane-bound nicotinic acetylcholine receptor [J].
Ulrich, H ;
Ippolito, JE ;
Pagán, OR ;
Eterovic, VA ;
Hann, RM ;
Shi, H ;
Lis, JT ;
Eldefrawi, ME ;
Hess, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14051-14056
[60]   3-DIMENSIONAL STRUCTURE OF THE COMPLEX OF 4-GUANIDINO-NEUSAC2EN AND INFLUENZA-VIRUS NEURAMINIDASE [J].
VARGHESE, JN ;
EPA, VC ;
COLMAN, PM .
PROTEIN SCIENCE, 1995, 4 (06) :1081-1087