Microbial carbohydrate-binding toxins - From etiology to biotechnological application

被引:5
作者
Danielewicz, Natalia [1 ,2 ]
Rosato, Francesca [3 ,4 ,5 ]
Dai, Wenyue [6 ,7 ]
Roemer, Winfried [3 ,4 ,5 ,8 ]
Turnbull, W. Bruce [6 ,7 ]
Mairhofer, Juergen [1 ]
机构
[1] EnGenes Biotech GmbH, Mooslackengasse 17, A-1190 Vienna, Austria
[2] Univ Nat Resources & Life Sci, Dept Biotechnol, Muthgasse 11, A-1190 Vienna, Austria
[3] Albert Ludwigs Univ Freiburg, Fac Biol, Schanzlestr 1, D-79104 Freiburg, Germany
[4] Albert Ludwigs Univ Freiburg, Signalling Res Ctr BIOSS, Schanzlestr 18, D-79104 Freiburg, Germany
[5] Albert Ludwigs Univ Freiburg, Signalling Res Ctr CIBSS, Schanzlestr 18, D-79104 Freiburg, Germany
[6] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
[7] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[8] Univ Freiburg, Freiburg Inst Adv Studies FRIAS, D-79104 Freiburg, Germany
关键词
Bacterial toxin; cholera toxin; shiga toxin; vaccine design; toxin-drug conjugate; downstream and upstream processing; fed-batch fermentation; HEAT-LABILE ENTEROTOXIN; UNCONJUGATED CHOLERA-TOXIN; VIBRIO-VULNIFICUS HEMOLYSIN; ESCHERICHIA-COLI; SHIGA-TOXIN; B-SUBUNIT; CRYSTAL-STRUCTURE; BORDETELLA-PERTUSSIS; BOTULINUM NEUROTOXIN; FUSION PROTEIN;
D O I
10.1016/j.biotechadv.2022.107951
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glycan-recognizing toxins play a significant role in the etiology of many diseases afflicting humanity. The carbohydrate recognition domains of these toxins play essential roles in the virulence of many microbial organisms with multiple modes of action, from promoting pore formation to facilitating the entry of toxic enzymatic subunits into the host cell. Carbohydrate-binding domains with an affinity for specific glycan-based receptors can also be exploited for various applications, including detecting glycobiomarkers, as drug delivery systems, and new generation biopharmaceutical products and devices (e.g. glycoselective capture of tumor-derived exosomes). Therefore, understanding how to efficiently express and purify recombinant toxins and their carbohydrate-binding domains can enable opportunities for the formulation of innovative biopharmaceuticals that can improve human health. Here, we provide an overview of carbohydrate-binding toxins in the context of biotechnological innovation. We review 1) structural characteristics concerning the toxins' mode of action; 2) applications and therapeutic design with a particular emphasis on exploiting carbohydrate-binding toxins for production of anti-tumor biopharmaceuticals; discuss 3) possible ways to manufacture those molecules at a bioreactor scale using microbial expression systems, and 4) their purification using their affinity for glycans.
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页数:18
相关论文
共 222 条
[51]   Shiga toxin-mediated retrograde delivery of a topoisomerase I inhibitor prodrug [J].
El Alaoui, Abdessamad ;
Schmidt, Frederic ;
Amessou, Mohamed ;
Sarr, Marianne ;
Decaudin, Didier ;
Florent, Jean-Claude ;
Johannes, Ludger .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (34) :6469-6472
[52]   PURIFICATION OF POLYMYXIN-RELEASED, HEAT-LABILE ENTEROTOXIN OF ESCHERICHIA-COLI [J].
EVANS, DJ ;
EVANS, DG ;
RICHARDSON, SH ;
GORBACH, SL .
JOURNAL OF INFECTIOUS DISEASES, 1976, 133 :S97-S102
[53]   Human colorectal tumors and metastases express Gb3 and can be targeted by an intestinal pathogen-based delivery tool [J].
Falguieres, Thomas ;
Maak, Matthias ;
von Weyhern, Claus ;
Sarr, Marianne ;
Sastre, Xavier ;
Poupon, Marie-France ;
Robine, Sylvie ;
Johannes, Ludger ;
Janssen, Klaus-Peter .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (08) :2498-2508
[54]   Penetration of protein toxins into cells [J].
Falnes, PO ;
Sandvig, K .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (04) :407-413
[55]   Distribution and neurochemical identification of pancreatic afferents in the mouse [J].
Fasanella, Kenneth E. ;
Christianson, Julie A. ;
Chanthaphavong, R. Savanh ;
Davis, Brian M. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2008, 509 (01) :42-52
[56]  
FINKELSTEIN RA, 1966, J IMMUNOL, V97, P25
[57]   PATHOGENESIS OF EXPERIMENTAL CHOLERA IN INFANT RABBITS .I. OBSERVATIONS ON INTRAINTESTINAL INFECTION + EXPERIMENTAL CHOLERA PRODUCED WITH CELL-FREE PRODUCTS [J].
FINKELSTEIN, RA ;
DUTTA, NK ;
NORRIS, HT .
JOURNAL OF INFECTIOUS DISEASES, 1964, 114 (03) :203-+
[58]   PRODUCTION OF HIGHLY PURIFIED CHOLERAGEN AND CHOLERAGENOID [J].
FINKELSTEIN, RA ;
LOSPALLU.JJ .
JOURNAL OF INFECTIOUS DISEASES, 1970, 121 :S63-+
[59]  
Florent J., 2012, Conjugates of the B-Subunit of Shiga Toxin for Anticancer Therapies, Patent No. [WO2014086952A1, 2014086952]
[60]   MONOAMINERGIC, PEPTIDERGIC, AND CHOLINERGIC AFFERENTS TO THE CAT FACIAL NUCLEUS AS EVIDENCED BY A DOUBLE IMMUNOSTAINING METHOD WITH UNCONJUGATED CHOLERA-TOXIN AS A RETROGRADE TRACER [J].
FORT, P ;
SAKAI, K ;
LUPPI, PH ;
SALVERT, D ;
JOUVET, M .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 283 (02) :285-302