antaRNA - Multi-objective inverse folding of pseudoknot RNA using ant-colony optimization

被引:18
|
作者
Kleinkauf, Robert [1 ]
Houwaart, Torsten [1 ]
Backofen, Rolf [1 ,2 ,3 ,4 ]
Mann, Martin [1 ]
机构
[1] Univ Freiburg, Dept Comp Sci, Bioinformat Grp, D-79110 Freiburg, Germany
[2] Univ Freiburg, Ctr Biol Signaling Studies BIOSS, D-79110 Freiburg, Germany
[3] Univ Freiburg, Ctr Biol Syst Anal ZBSA, D-79110 Freiburg, Germany
[4] Univ Copenhagen, Ctr Noncoding RNA Technol & Hlth, DK-1870 Frederiksberg C, Denmark
来源
BMC BIOINFORMATICS | 2015年 / 16卷
关键词
Pseudoknot RNA; Inverse folding RNA; RNAdesign; Synthetic biology; Biotechnology; DESIGN; SERVER;
D O I
10.1186/s12859-015-0815-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Many functional RNA molecules fold into pseudoknot structures, which are often essential for the formation of an RNA's 3D structure. Currently the design of RNA molecules, which fold into a specific structure (known as RNA inverse folding) within biotechnological applications, is lacking the feature of incorporating pseudoknot structures into the design. Hairpin-(H)- and kissing hairpin-(K)- type pseudoknots cover a wide range of biologically functional pseudoknots and can be represented on a secondary structure level. Results: The RNA inverse folding program antaRNA, which takes secondary structure, target GC-content and sequence constraints as input, is extended to provide solutions for such H- and K-type pseudoknotted secondary structure constraint. We demonstrate the easy and flexible interchangeability of modules within the antaRNA framework by incorporating pKiss as structure prediction tool capable of predicting the mentioned pseudoknot types. The performance of the approach is demonstrated on a subset of the Pseudobase++ dataset. Conclusions: This new service is available via a standalone version and is also part of the Freiburg RNA Tools webservice. Furthermore, antaRNA is available in Galaxy and is part of the RNA-workbench Docker image.
引用
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页数:7
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