Crosslinker-modified nucleic acid probes for improved target identification and biomarker detection

被引:14
作者
Elskens, Joke [1 ]
Madder, Annemieke [1 ]
机构
[1] Univ Ghent, Fac Sci, Dept Organ & Macromol Chem, Krijgslaan 281 Bldg S4, B-9000 Ghent, Belgium
来源
RSC CHEMICAL BIOLOGY | 2021年 / 2卷 / 02期
关键词
LONG NONCODING RNAS; LINKING REACTION; PHOTOAFFINITY PROBES; COVALENT CAPTURE; ABASIC SITES; DNA; PROTEIN; OLIGONUCLEOTIDE; COUMARIN; DUPLEX;
D O I
10.1039/d0cb00236d
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the intricate interaction pattern of nucleic acids with other molecules is essential to gain further insight in biological processes and disease mechanisms. To this end, a multitude of hybridization-based assays have been designed that rely on the non-covalent recognition between complementary nucleic acid sequences. However, the ephemeral nature of these interactions complicates straightforward analysis as low efficiency and specificity are rule rather than exception. By covalently locking nucleic acid interactions by means of a crosslinking agent, the overall efficiency, specificity and selectivity of hybridization-based assays could be increased. In this mini-review we highlight methodologies that exploit the use of crosslinker-modified nucleic acid probes for interstrand nucleic acid crosslinking with the objective to study, detect and identify important targets as well as nucleic acid sequences that can be considered relevant biomarkers. We emphasize on the usefulness and advantages of crosslinking agents and elaborate on the chemistry behind the crosslinking reactions they induce.
引用
收藏
页码:410 / 422
页数:13
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