4.7 Article

MPBind: a Meta-motif-based statistical framework and pipeline to Predict Binding potential of SELEX-derived aptamers

Journal

BIOINFORMATICS
Volume 30, Issue 18, Pages 2665-2667

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btu348

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Funding

  1. Morgridge Institute for Research
  2. Institute for Collaborative Biotechnologies through the Army Research Office
  3. Garland Initiative at UCSB
  4. NIH [1U54DK093467]

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A Summary: Aptamers are 'synthetic antibodies' that can bind to target molecules with high affinity and specificity. Aptamers are chemically synthesized and their discovery can be performed completely in vitro, rather than relying on in vivo biological processes, making them well-suited for high-throughput discovery. However, a large fraction of the most enriched aptamers in Systematic Evolution of Ligands by EXponential enrichment (SELEX) rounds display poor binding activity. Here, we present MPBind, a Meta-motif-based statistical framework and pipeline to Predict the Binding potential of SELEX-derived aptamers. Using human embryonic stem cell SELEX-Seq data, MPBind achieved high prediction accuracy for binding potential. Further analysis showed that MPBind is robust to both polymerase chain reaction amplification bias and incomplete sequencing of aptamer pools. These two biases usually confound aptamer analysis.

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