Literature DB >> 30942916

Bismaleimide cross-linked anthrax toxin forms functional octamers with high specificity in tumor targeting.

Elyse S Fischer1, Warren A Campbell1, Shihui Liu2, Rodolfo Ghirlando3, Rasem J Fattah1, Thomas H Bugge2, Stephen H Leppla1.   

Abstract

In recent years, anthrax toxin has been reengineered to act as a highly specific antiangiogenic cancer therapeutic, shown to kill tumors in animal models. This has been achieved by modifying protective antigen (PA) so that its activation and toxicity require the presence of two proteases, matrix metalloproteinase (MMP) and urokinase plasminogen activator (uPA), which are upregulated in tumor microenvironments. These therapeutics consist of intercomplementing PA variants, which are individually nontoxic, but form functional toxins upon complementary oligomerization. Here, we have created a dual-protease requiring PA targeting system which utilizes bismaleimide cross-linked PA (CLPA) rather than the intercomplementing PA variants. Three different CLPA agents were tested and, as expected, found to exclusively form octamers. Two of the CLPA agents have in vitro toxicities equal to those of previous intercomplementing agents, while the third CLPA agent had compromised in vitro cleavage and was significantly less cytotoxic. We hypothesize this difference was due to steric hindrance caused by cross-linking two PA monomers in close proximity to the PA cleavage site. Overall, this work advances the development and use of the PA and LF tumor-targeting system as a practical cancer therapeutic, as it provides a way to reduce the drug components of the anthrax toxin drug delivery system from three to two, which may lower the cost and simplify testing in clinical trials. HIGHLIGHT: Previously, anthrax toxin has been reengineered to act as a highly specific antiangiogenic cancer therapeutic. Here, we present a version, which utilizes bismaleimide cross-linked protective antigen (PA) rather than intercomplementing PA variants. This advances the development of anthrax toxin as a practical cancer therapeutic as it reduces the components of the drug delivery system to two, which may lower the cost and simplify testing in clinical trials.
© 2019 The Protein Society.

Entities:  

Keywords:  anthrax toxin; bismaleimide cross-linker; cancer therapy; matrix metalloprotease; oligomerization; protective antigen; urokinase plasminogen activator

Mesh:

Substances:

Year:  2019        PMID: 30942916      PMCID: PMC6511737          DOI: 10.1002/pro.3613

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  48 in total

Review 1.  Anthrax lethal and edema toxins in anthrax pathogenesis.

Authors:  Shihui Liu; Mahtab Moayeri; Stephen H Leppla
Journal:  Trends Microbiol       Date:  2014-03-27       Impact factor: 17.079

2.  Tobacco etch virus protease: mechanism of autolysis and rational design of stable mutants with wild-type catalytic proficiency.

Authors:  R B Kapust; J Tözsér; J D Fox; D E Anderson; S Cherry; T D Copeland; D S Waugh
Journal:  Protein Eng       Date:  2001-12

3.  A urokinase-activated recombinant anthrax toxin is selectively cytotoxic to many human tumor cell types.

Authors:  Ralph J Abi-Habib; Ravibhushan Singh; Shihui Liu; Thomas H Bugge; Stephen H Leppla; Arthur E Frankel
Journal:  Mol Cancer Ther       Date:  2006-10       Impact factor: 6.261

4.  Anthrax lethal factor cleaves the N-terminus of MAPKKs and induces tyrosine/threonine phosphorylation of MAPKs in cultured macrophages.

Authors:  G Vitale; R Pellizzari; C Recchi; G Napolitani; M Mock; C Montecucco
Journal:  Biochem Biophys Res Commun       Date:  1998-07-30       Impact factor: 3.575

5.  Cytotoxicity of the matrix metalloproteinase-activated anthrax lethal toxin is dependent on gelatinase expression and B-RAF status in human melanoma cells.

Authors:  Randall W Alfano; Stephen H Leppla; Shihui Liu; Thomas H Bugge; Meenhard Herlyn; Keiran S Smalley; Jennifer L Bromberg-White; Nicholas S Duesbery; Arthur E Frankel
Journal:  Mol Cancer Ther       Date:  2008-05       Impact factor: 6.261

6.  Mapping dominant-negative mutations of anthrax protective antigen by scanning mutagenesis.

Authors:  Michael Mourez; Ming Yan; D Borden Lacy; Lisa Dillon; Lori Bentsen; Amy Marpoe; Clémence Maurin; Eileen Hotze; Darran Wigelsworth; Ruth-Anne Pimental; Jimmy D Ballard; R John Collier; Rodney K Tweten
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-17       Impact factor: 11.205

7.  Anthrax edema factor toxicity is strongly mediated by the N-end rule.

Authors:  Clinton E Leysath; Damilola D Phillips; Devorah Crown; Rasem J Fattah; Mahtab Moayeri; Stephen H Leppla
Journal:  PLoS One       Date:  2013-08-28       Impact factor: 3.240

8.  Efficient cell-specific uptake of binding proteins into the cytoplasm through engineered modular transport systems.

Authors:  Wouter P R Verdurmen; Manuel Luginbühl; Annemarie Honegger; Andreas Plückthun
Journal:  J Control Release       Date:  2014-12-17       Impact factor: 11.467

9.  Residues 1-254 of anthrax toxin lethal factor are sufficient to cause cellular uptake of fused polypeptides.

Authors:  N Arora; S H Leppla
Journal:  J Biol Chem       Date:  1993-02-15       Impact factor: 5.486

10.  Anti-tumor activity of anthrax toxin variants that form a functional translocation pore by intermolecular complementation.

Authors:  Shihui Liu; Qian Ma; Rasem Fattah; Thomas H Bugge; Stephen H Leppla
Journal:  Oncotarget       Date:  2017-05-09
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