TY - JOUR
T1 - Nanogel-Facilitated Protein Intracellular Specific Degradation through Trim-Away
AU - Sui, Binglin
AU - Wang, Mingming
AU - Cheng, Chen
AU - Zhang, Quanguang
AU - Zhang, Jiajia
AU - Fan, Daping
AU - Xu, Peisheng
N1 - Funding Information:
B.S. and M.W. contributed equally to this work. The authors want to thank National Institutes of Health (1R01AG054839‐01A1, 1R41CA254500‐01A1, and 1R21CA252360‐01) for financial support of the research.
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/7/23
Y1 - 2021/7/23
N2 - The recently discovered “Trim-Away” mechanism opens a new window for fast and selective degradation of endogenous proteins. However, the in vivo and clinical application of this approach is hindered by the requirement of special skills and equipment needed for the intracellular delivery of antibodies. Here, an antibody conjugated polymer nanogel system, nanogel-facilitated protein intracellular specific degradation (Nano-ERASER), for intracellular delivery and release of antibody, and degradation of a specific endogenous protein is developed. After being delivered into cells, the antibody is released and forms a complex with its target protein, and subsequently binds to the Fc receptor of Tripartite motif 21 (TRIM21). The resulting complex of target protein/antibody/TRIM21 is then degraded by the proteasome. The efficacy of Nano-ERASER is validated by depleting GFP protein in a GFP expressing cell line. Furthermore, Nano-ERASER successfully degrades the coatomer protein complex ζ1, a vital protein for cancer cells, and kills those cells while sparing normal cells. Benefitting from its convenience and targeted delivery merit, Nano-ERASER technique is promising in providing a reliable tool for endogenous protein function study as well as paves the way for novel antibody-based Trim-Away therapeutic modalities for cancer and other diseases.
AB - The recently discovered “Trim-Away” mechanism opens a new window for fast and selective degradation of endogenous proteins. However, the in vivo and clinical application of this approach is hindered by the requirement of special skills and equipment needed for the intracellular delivery of antibodies. Here, an antibody conjugated polymer nanogel system, nanogel-facilitated protein intracellular specific degradation (Nano-ERASER), for intracellular delivery and release of antibody, and degradation of a specific endogenous protein is developed. After being delivered into cells, the antibody is released and forms a complex with its target protein, and subsequently binds to the Fc receptor of Tripartite motif 21 (TRIM21). The resulting complex of target protein/antibody/TRIM21 is then degraded by the proteasome. The efficacy of Nano-ERASER is validated by depleting GFP protein in a GFP expressing cell line. Furthermore, Nano-ERASER successfully degrades the coatomer protein complex ζ1, a vital protein for cancer cells, and kills those cells while sparing normal cells. Benefitting from its convenience and targeted delivery merit, Nano-ERASER technique is promising in providing a reliable tool for endogenous protein function study as well as paves the way for novel antibody-based Trim-Away therapeutic modalities for cancer and other diseases.
KW - TRIM21
KW - antibody delivery
KW - intracellular release
KW - nanogel
KW - protein degradation
UR - http://www.scopus.com/inward/record.url?scp=85105911536&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85105911536&partnerID=8YFLogxK
U2 - 10.1002/adfm.202010556
DO - 10.1002/adfm.202010556
M3 - Article
AN - SCOPUS:85105911536
SN - 1616-301X
VL - 31
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 30
M1 - 2010556
ER -