An Antibody-CRISPR/Cas Conjugate Platform for Target-Specific Delivery and Gene Editing in Canceropen access
- Authors
- Yang, Seungju; Im, San Hae; Chung, Ju Yeon; Lee, Juhee; Lee, Kyung-Hun; Kang, Yoo Kyung; Chung, Hyun Jung
- Issue Date
- Jun-2024
- Publisher
- Wiley-VCH Verlag
- Keywords
- antibody conjugation; cancer therapy; CRISPR/Cas; in vivo gene editing; specific delivery
- Citation
- Advanced Science, v.11, no.21
- Indexed
- SCIE
SCOPUS
- Journal Title
- Advanced Science
- Volume
- 11
- Number
- 21
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/70221
- DOI
- 10.1002/advs.202308763
- ISSN
- 2198-3844
- Abstract
- The CRISPR/Cas system has been introduced as an innovative tool for therapy, however achieving specific delivery to the target has been a major challenge. Here, an antibody-CRISPR/Cas conjugate platform that enables specific delivery and target gene editing in HER2-positive cancer is introduced. The CRISPR/Cas system by replacing specific residues of Cas9 with an unnatural amino acid is engineered, that can be complexed with a nanocarrier and bioorthogonally functionalized with a monoclonal antibody targeting HER2. The resultant antibody-conjugated CRISPR/Cas nanocomplexes can be specifically delivered and induce gene editing in HER2-positive cancer cells in vitro. It is demonstrated that the in vivo delivery of the antibody-CRISPR/Cas nanocomplexes can effectively disrupt the plk1 gene in HER2-positive ovarian cancer, resulting in substantial suppression of tumor growth. The current study presents a useful therapeutic platform for antibody-mediated delivery of CRISPR/Cas for the treatment of various cancers and genetic diseases. Here, an antibody-CRISPR/Cas conjugate platform that enables specific delivery and target gene editing in HER2-positive cancer is introduced. It is demonstrated that the in vivo delivery of the antibody-CRISPR/Cas nanocomplexes can effectively disrupt the plk1 gene in HER2-positive ovarian cancer, resulting in substantial suppression of tumor growth. image
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