Expression of the First Recombinant Anti-Tumoral Snake Venom Kunitz-Type Serine Protease Inhibitor

被引:10
作者
Morjen, Maram [1 ]
Moslah, Wassim [1 ]
Touihri-Baraketi, Imen [2 ]
Srairi-Abid, Najet [1 ]
Luis, Jose [3 ]
Marrakchi, Naziha [1 ,4 ]
Jebali, Jed [1 ]
机构
[1] Univ Tunis El Manar, Pasteur Inst Tunis, Lab Biomol Venoms & Theranost Applicat, LR20IPT01, Tunis 1002, Tunisia
[2] Inst Natl Rech & Anal Phys Chim INRAP, Lab Subst Nat, Sidi Thabet 2020, Ariana, Tunisia
[3] Univ Aix Marseille, Inst Neuro Physiopathol INP, CNRS, UMR 7051, 27 Bd Jean Moulin, F-13385 Marseille, France
[4] Univ Tunis El Manar, Med Sch Tunis, 15 Djebel Lakhdhar,St La Rabta, Tunis 1007, Tunisia
关键词
snake venom; Kunitz-type serine protease inhibitor; recombinant PIVL; tumorogenesis; DENDROTOXIN-K; CELL-ADHESION; MIGRATION; CLONING; PIVL;
D O I
10.3390/toxins14030170
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
PIVL is a Kunitz-type serine protease inhibitor that was previously characterized from Tunisian snake venom, Macrovipera lebetina transmediterranea. It reduced glioblastoma cells' development and significantly blocked angiogenesis in in-vitro and ex-vivo models. PIVL exerted these effects by interfering with alpha v beta 3 integrin. In order to produce a biological active recombinant, the cDNA cloning and expression of PIVL was performed in Escherichia coli (BL21)-DE3 cells using pET-22b (+) vector. The recombinant PIVL protein (rPIVL) was purified by nickel affinity chromatography and has recognized monoclonal anti-His antibody. Functionally, rPIVL exhibited potent anti-tumor cell effects as well as anti-angiogenesis properties. Interestingly, we found that both native PIVL (nPIVL) and rPIVL modulated PI3/AKT and MAPK signaling pathways. In all, our results showed that we have successfully expressed the first active anti-oncogenic snake venom Kunitz-type protease inhibitor that can be a potential therapeutic drug against glioblastoma, in its native or recombinant form.
引用
收藏
页数:12
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