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Updated: Feb 13, 2026

Protocols for C-Brick DNA Standard Assembly Using Cpf1
Published on: June 15, 2017
Base editing with a Cpf1-cytidine deaminase fusion
Xiaosa Li1,2,3, Ying Wang4, Yajing Liu1,2,3
1School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Abstract:
The targeting range of CRISPR-Cas9 base editors (BEs) is limited by their G/C-rich protospacer-adjacent motif (PAM) sequences. To overcome this limitation, we developed a CRISPR-Cpf1-based BE by fusing the rat cytosine deaminase APOBEC1 to a catalytically inactive version of Lachnospiraceae bacterium Cpf1. The base editor recognizes a T-rich PAM sequence and catalyzes C-to-T conversion in human cells, while inducing low levels of indels, non-C-to-T substitutions and off-target editing.
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