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Updated: Aug 30, 2025

A Customizable Protocol for String Assembly gRNA Cloning STAgR
Published on: December 26, 2018
PARA: A New Platform for the Rapid Assembly of gRNA Arrays for Multiplexed CRISPR Technologies
Guoliang Yuan1,2, Stanton Martin1,2, Md Mahmudul Hassan1,2,3
1Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
Abstract:
Multiplexed CRISPR technologies have great potential for pathway engineering and genome editing. However, their applications are constrained by complex, laborious and time-consuming cloning steps. In this research, we developed a novel method, PARA, which allows for the one-step assembly of multiple guide RNAs (gRNAs) into a CRISPR vector with up to 18 gRNAs. Here, we demonstrate that PARA is capable of the efficient assembly of transfer RNA/Csy4/ribozyme-based gRNA arrays. To aid in this process and to streamline vector construction, we developed a user-friendly PARAweb tool for designing PCR primers and component DNA parts and simulating assembled gRNA arrays and vector sequences.
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