| Literature DB >> 31711233 |
Kyungbo Kim1,2, Pereira Araujo3, Nikhil Hebbar3, Ziyuan Zhou1,2, Xirong Zheng1,2, Fang Zheng1,2, Vivek M Rangnekar3,4,5,6, Chang-Guo Zhan1,2.
Abstract
Prostate apoptosis response-4 (Par-4) is a tumor suppressor which protects against neoplastic transformation. Remarkably, Par-4 is capable of inducing apoptosis selectively in cancer cells without affecting the normal cells. In this study, we found that recombinant Par-4 protein had limited serum persistence in mice that may diminish its anti-tumor activity in vivo. To improve the in vivo performance of the short-lived Par-4 protein, we aimed to develop a novel, long-lasting form of Par-4 with extended sequence, denoted as Par-4Ex, without affecting the desirable molecular function of the natural Par-4. We demonstrate that the Par-4Ex protein entity, produced by using the Escherichia coli expression system suitable for large-scale production, fully retains the desirable pro-apoptotic activity of Par-4 protein, but with ~7-fold improved biological half-life. Further in vivo tests confirmed that, due to the prolonged biological half-life, the Par-4Ex protein is indeed more potent in suppressing metastatic tumor growth in mice.Entities:
Keywords: Par-4; biological half-life; metastatic cancer; protein engineering; therapeutic protein
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Year: 2019 PMID: 31711233 PMCID: PMC7191865 DOI: 10.1093/protein/gzz034
Source DB: PubMed Journal: Protein Eng Des Sel ISSN: 1741-0126 Impact factor: 1.650