Engineering T4 Bacteriophage for <i>In Vivo</i> Display by Type V CRISPR-Cas Genome Editing.

ABSTRACT: Bacteriophage T4 has enormous potential for biomedical applications due to its large size, capsid architecture, and high payload capability for protein and DNA delivery. However, it is not very easy to genetically engineer its genome heavily modified by cytosine hydroxymethylation and glucosylation. The glucosyl hydroxymethyl cytosine (ghmC) genome of phage is completely resistant to most restriction endonucleases and exhibits various degrees of resistance to CRISPR-Cas systems. Here, we found that the type V CRISPR-Cas12a system, which shows efficient cleavage of ghmC-modified genome when compared to the type II CRISPR-Cas9 system, can be synergistically employed to generate recombinant T4 phages. Focused on surface display, we analyzed the ability of phage T4 outer capsid proteins Hoc (h

SUBMITTER: Dong J 

PROVIDER: S-EPMC12867177 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature