Microcystins: Synthesis and structure-activity relationship studies toward PP1 and PP2A

被引:63
作者
Fontanillo, Miriam [1 ]
Koehn, Maja [1 ,2 ,3 ]
机构
[1] European Mol Biol Lab, Genome Biol Unit, Meyerhofstr 1, D-69117 Heidelberg, Germany
[2] Univ Freiburg, Ctr Biol Signalling Studies BIOSS, Schanzlestr 18, D-79104 Freiburg, Germany
[3] Univ Freiburg, Fac Biol, Schanzlestr 1, D-79104 Freiburg, Germany
基金
欧洲研究理事会;
关键词
Microcystin; Protein phosphatases; Inhibitors; Structure-activity relationship; Medicinal chemistry; PROTEIN PHOSPHATASE 2A; SER-THR PHOSPHATASES; PRIMARY LIVER-CANCER; N-BOC-ADDA; OKADAIC ACID; AMINO-ACID; CYCLIC-PEPTIDES; MOLECULAR-MECHANISMS; CRYSTAL-STRUCTURE; TOXIN STRUCTURES;
D O I
10.1016/j.bmc.2017.08.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microcystins are highly toxic cyanotoxins responsible for plant, animal and human poisoning. Exposure to microcystins, mainly through drinkable water and contaminated food, is a current world health concern. Although it is quite challenging, the synthesis of these potent cyanotoxins, analogs and derivatives helps to evaluate their toxicological properties and to elucidate their binding mechanisms to their main targets Protein Phosphatase-1 (PP1) and -2A (PP2A). This review focuses on synthetic approaches to prepare microcystins and analogs and compiles structure-activity relationship (SAR) studies that describe the unique features of microcystins that make them so potent. (C) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:1118 / 1126
页数:9
相关论文
共 128 条
[1]   The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: Rational modifications imparting PP1 selectivity [J].
Aggen, JB ;
Humphrey, JM ;
Gauss, CM ;
Huang, HB ;
Nairn, AC ;
Chamberlain, AR .
BIOORGANIC & MEDICINAL CHEMISTRY, 1999, 7 (03) :543-564
[2]   Exploring the natural role of microcystins -: A review of effects on photoautotrophic organisms [J].
Babica, P ;
Bláha, L ;
Marsálek, B .
JOURNAL OF PHYCOLOGY, 2006, 42 (01) :9-20
[3]   A molecular basis for different interactions of marine toxins with protein phosphatase-1 - Molecular models for bound motuporin, microcystins, okadaic acid, and calyculin A [J].
Bagu, JR ;
Sykes, BD ;
Craig, MM ;
Holmes, CFB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :5087-5097
[4]   COMPARISON OF THE SOLUTION STRUCTURES OF MICROCYSTIN-LR AND MOTUPORIN [J].
BAGY, JR ;
SONNICHSEN, FD ;
WILLIAMS, D ;
ANDERSEN, RJ ;
SYKES, BD ;
HOLMES, CFB .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (02) :114-116
[5]  
BEATTY MF, 1992, J CHEM SOC PERK T 1, P1637
[6]   Phytotoxicity associated to microcystins: a review [J].
Bittencourt-Oliveira, M. C. ;
Hereman, T. C. ;
Cordeiro-Araujo, M. K. ;
Macedo-Silva, I ;
Dias, C. T. ;
Sasaki, F. F. C. ;
Moura, A. N. .
BRAZILIAN JOURNAL OF BIOLOGY, 2014, 74 (04) :753-760
[7]   The extended PP1 toolkit: designed to create specificity [J].
Bollen, Mathieu ;
Peti, Wolfgang ;
Ragusa, Michael J. ;
Beullens, Monique .
TRENDS IN BIOCHEMICAL SCIENCES, 2010, 35 (08) :450-458
[8]   Enzymatic pathway for the bacterial degradation of the cyanobacterial cyclic peptide toxin microcystin LR [J].
Bourne, DG ;
Jones, GJ ;
Blakeley, RL ;
Jones, A ;
Negri, AP ;
Riddles, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (11) :4086-4094
[9]   Protein Ser/Thr phosphatases - the ugly ducklings of cell signalling [J].
Brautigan, David L. .
FEBS JOURNAL, 2013, 280 (02) :324-345
[10]   Molecular Mechanisms of Microcystin Toxicity in Animal Cells [J].
Campos, Alexandre ;
Vasconcelos, Vitor .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2010, 11 (01) :268-287