Lanthanide ions as required cofactors for DNA catalysts

被引:64
作者
Dokukin, Victor [1 ]
Silverman, Scott K. [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ZN2+-DEPENDENT DEOXYRIBOZYMES; CRYSTAL-STRUCTURE; STRAND SCISSION; HUMAN URACIL; HYDROLYSIS; GLYCOSYLASE; RNA; REPAIR; ENZYMES; RECOGNITION;
D O I
10.1039/c2sc01067d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report that micromolar concentrations of lanthanide ions can be required cofactors for DNA-hydrolyzing deoxyribozymes. Previous work identified deoxyribozymes that simultaneously require both Zn2+ and Mn2+ to achieve DNA-catalyzed DNA hydrolysis (10 12 rate enhancement); a mutant of one such DNA catalyst requires only Zn2+. Here we show that in vitro selection in the presence of 10 mu M lanthanide ion (Ce3+, Eu3+, or Yb3+) along with 1 mM Zn2+ leads to numerous DNA-hydrolyzing deoxyribozymes that strictly require the lanthanide ion as well as Zn2+ for catalytic activity. These DNA catalysts have a range of lanthanide dependences, including some deoxyribozymes that strongly favor one particular lanthanide ion (e.g., Ce3+ >> Eu3+ >> Yb3+) and others that function well with more than one lanthanide ion. Intriguingly, two of the Yb3+-dependent deoxyribozymes function well with Yb3+ alone (Kd,app similar to 10 mM, in the absence of Zn2+) and have little or no activity with Eu3+ or Ce3+. In contrast to these selection outcomes when lanthanide ions were present, new selections with Zn2+ or Mn2+ alone, or Zn2+ with Mg2+/Ca2+, led primarily to deoxyribozymes that cleave DNA by deglycosylation and beta-elimination rather than by hydrolysis, including several instances of depyrimidination. We conclude that lanthanide ions warrant closer attention as cofactors when identifying new nucleic acid catalysts, especially for applications in which high concentrations of polyvalent metal ion cofactors are undesirable.
引用
收藏
页码:1707 / 1714
页数:8
相关论文
共 40 条
[1]   Toward a detailed understanding of base excision repair enzymes: transition state and mechanistic analyses of N-glycoside hydrolysis and N-glycoside transfer [J].
Berti, PJ ;
McCann, JAB .
CHEMICAL REVIEWS, 2006, 106 (02) :506-555
[2]  
Breaker R R, 1994, Chem Biol, V1, P223, DOI 10.1016/1074-5521(94)90014-0
[3]   Oxidative nucleobase modifications leading to strand scission [J].
Burrows, CJ ;
Muller, JG .
CHEMICAL REVIEWS, 1998, 98 (03) :1109-1151
[4]   DNA-catalyzed sequence-specific hydrolysis of DNA [J].
Chandra, Madhavaiah ;
Sachdeva, Amit ;
Silverman, Scott K. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (10) :718-720
[5]   DNA base repair - recognition and initiation of catalysis [J].
Dalhus, Bjorn ;
Laerdahl, Jon K. ;
Backe, Paul H. ;
Bjoras, Magnar .
FEMS MICROBIOLOGY REVIEWS, 2009, 33 (06) :1044-1078
[6]   Probing the binding of Tb(III) and Eu(III) to the hammerhead ribozyme using luminescence spectroscopy [J].
Feig, AL ;
Panek, M ;
Horrocks, WD ;
Uhlenbeck, OC .
CHEMISTRY & BIOLOGY, 1999, 6 (11) :801-810
[7]   DNA-catalyzed hydrolysis of DNA phosphodiesters [J].
Fekry, Mostafa I. ;
Gates, Kent S. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (10) :710-711
[8]   Deoxyribozymes with 2′-5′ RNA ligase activity [J].
Flynn-Charlebois, A ;
Wang, YM ;
Prior, TK ;
Rashid, I ;
Hoadley, KA ;
Coppins, RL ;
Wolf, AC ;
Silverman, SK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (09) :2444-2454
[9]   Lanthanide-mediated DNA hydrolysis [J].
Franklin, SJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (02) :201-208
[10]   Detection of Damaged DNA Bases by DNA Glycosylase Enzymes [J].
Friedman, Joshua I. ;
Stivers, James T. .
BIOCHEMISTRY, 2010, 49 (24) :4957-4967