Advancing Small-Molecule-Based Chemical Biology with Next-Generation Sequencing Technologies

被引:19
作者
Anandhakumar, Chandran [1 ]
Kizaki, Seiichiro [1 ]
Bando, Toshikazu [1 ]
Pandian, Ganesh N. [2 ]
Sugiyama, Hiroshi [1 ,2 ]
机构
[1] Kyoto Univ, Dept Chem, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
[2] Kyoto Univ, Inst Integrated Cell Mat Sci ICeMS, Sakyo Ku, Kyoto 6068501, Japan
关键词
aptamers; chemical biology; genomics; next-generation sequencing; small molecules; DNA-BINDING MOLECULES; IN-VITRO SELECTION; GENE-EXPRESSION; CHIP-SEQ; SPATIAL-ORGANIZATION; APTAMER SELECTION; EMERGING CLASS; RNA MOLECULES; GROWTH-FACTOR; HIGH-AFFINITY;
D O I
10.1002/cbic.201402556
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
Next-generation-sequencing (NGS) technologies enable us to obtain extensive information by deciphering millions of individual DNA sequencing reactions simultaneously. The new DNA-sequencing strategies exceed their precursors in output by many orders of magnitude, resulting in a quantitative increase in valuable sequence information that could be harnessed for qualitative analysis. Sequencing on this scale has facilitated significant advances in diverse disciplines, ranging from the discovery, design, and evaluation of many small molecules and relevant biological mechanisms to maturation of personalized therapies. NGS technologies that have recently become affordable allow us to gain in-depth insight into small-molecule-triggered biological phenomena and empower researchers to develop advanced versions of small molecules. In this review we focus on the overlooked implications of NGS technologies in chemical biology, with a special emphasis on small-molecule development and screening.
引用
收藏
页码:20 / 38
页数:19
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