Bioengineered protein phosphatase 2A Update on need

被引:1
|
作者
Rubiolo, Juan A. [1 ]
Lopez-Alonso, Henar [2 ]
Alfonso, Amparo [2 ]
Vega, Felix V. [1 ]
Vieytes, Mercedes Rodriguez [1 ]
Botana, Luis M. [2 ]
机构
[1] Fac Vet, Dept Fisiol, Lugo, Spain
[2] Fac Vet, Dept Farmacol, Lugo, Spain
关键词
recombinant PP2AC; insect larvae; harmful algal blooms; eutrophication; natural toxin detection; CATALYTIC SUBUNIT-ALPHA; HARMFUL ALGAL BLOOMS; OKADAIC ACID; FUNCTIONAL EXPRESSION; INHIBITION ASSAY; POTENT INHIBITOR; IDENTIFICATION; HEALTH; PURIFICATION; CLIMATE;
D O I
10.4161/bioe.22461
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
Harmful algal blooms caused by phytoplankton can occur in all aquatic environments. Some of the algae present in these blooms are capable of producing extremely potent toxins. Due to climate change and eutrophication, harmful algal blooms are increasing on a global scale. One kind of toxin producing algae are those that produce okadaic acid, its derivatives (dinophysistoxin-1 and 2), and microcystins. These toxins are potent inhibitors of protein phosphatase 2A, so this protein is used to detect the mentioned toxins in natural samples. Originally protein phosphatase 2A purified from animal tissues was used, but enzyme activity and stability fluctuations prevented the use of the enzyme in detection kits. Expression of the enzyme as a recombinant protein provided a solution to this problem. For this purpose, several strategies have been followed. We evaluated the activity, specificity and stability of the human protein phosphatase 2A catalytic subunit a expressed in insect larvae and showed that this expression system can be a reliable source of high quantities of stable enzyme.
引用
收藏
页码:72 / 77
页数:6
相关论文
共 50 条
  • [31] Protein Phosphatase 2A as a Potential Target for Anticancer Therapy
    Kalev, Peter
    Sablina, Anna A.
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2011, 11 (01) : 38 - 46
  • [32] Protein phosphatase 2A, a novel and unexplored anticancer target
    Sakoff, JA
    Ackland, SP
    Garg, MB
    Walkom, CC
    McCluskey, A
    EUROPEAN JOURNAL OF CANCER, 2002, 38 : S94 - S94
  • [33] Protein phosphatase 2A may participate in hepatocytic differentiation
    Enjoji, M
    Nakamuta, M
    Nawata, H
    IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2002, 38 (01) : 5 - 6
  • [34] Protein phosphatase 2A may participate in hepatocytic differentiation
    Munechika Enjoji
    Makoto Nakamuta
    Hajime Nawata
    In Vitro Cellular & Developmental Biology - Animal, 2002, 38 (1) : 5 - 6
  • [35] Inhibition of Protein Phosphatase 2A: Focus on the Glutamatergic System
    Zimmer, Eduardo R.
    Leuzy, Antoine
    Souza, Diogo O.
    Portela, Luis V.
    MOLECULAR NEUROBIOLOGY, 2016, 53 (06) : 3753 - 3755
  • [36] Total Synthesis of the Protein Phosphatase 2A Inhibitor Lactodehydrothyrsiferol
    Clausen, Dane J.
    Wan, Shuangyi
    Floreancig, Paul E.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (22) : 5178 - 5181
  • [37] Adenosinergic modulation of protein phosphatase 2A in the murine heart
    Tikh, Eugene I.
    Fenton, Richard A.
    Dobson, James G., Jr.
    FASEB JOURNAL, 2007, 21 (06): : A793 - A793
  • [38] A METAL-DEPENDENT FORM OF PROTEIN PHOSPHATASE 2A
    CAI, LW
    CHU, YF
    WILSON, SE
    SCHLENDER, KK
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (01) : 274 - 279
  • [39] The Structure of Protein Phosphatase 2A and Its Inhibition of Tumorigenesis
    Li Tian-Zhu
    Xiang Ben-Qiong
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2009, 36 (02) : 133 - 142
  • [40] Shugoshin collaborates with protein phosphatase 2A to protect cohesin
    Laboratory of Chromosome Dynamics, Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Tokyo 113-0032, Japan
    不详
    不详
    不详
    Nature, 2006, 1 (46-52)