4.7 Article

How to Find the Right RNA-Sensing CRISPR-Cas System for an In Vitro Application

Journal

BIOSENSORS-BASEL
Volume 12, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/bios12020053

Keywords

RNA sensing; CRISPR-Cas; spacer; in vitro; PAM; sensor design

Funding

  1. King Abdullah University of Science and Technology (KAUST) through the baseline fund [REI/1/4204-01]
  2. Office of Sponsored Research (OSR)

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CRISPR-Cas systems have great potential for RNA biosensing, but there is currently no systematic guide for selecting the most appropriate RNA-targeting CRISPR-Cas system. This study proposes a set of systematic selection criteria and identifies four candidates for in vitro RNA.
CRISPR-Cas systems have a great and still largely untapped potential for in vitro applications, in particular, for RNA biosensing. However, there is currently no systematic guide on selecting the most appropriate RNA-targeting CRISPR-Cas system for a given application among thousands of potential candidates. We provide an overview of the currently described Cas effector systems and review existing Cas-based RNA detection methods. We then propose a set of systematic selection criteria for selecting CRISPR-Cas candidates for new applications. Using this approach, we identify four candidates for in vitro RNA.

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