CHEMICAL MODIFICATION OF HAMMERHEAD RIBOZYMES - CATALYTIC ACTIVITY AND NUCLEASE RESISTANCE

被引:200
|
作者
BEIGELMAN, L
MCSWIGGEN, JA
DRAPER, KG
GONZALEZ, C
JENSEN, K
KARPEISKY, AM
MODAK, AS
MATULICADAMIC, J
DIRENZO, AB
HAEBERLI, P
SWEEDLER, D
TRACZ, D
GRIMM, S
WINCOTT, FE
THACKRAY, VG
USMAN, N
机构
[1] RIBOZYME PHARMACEUT INC,DEPT CHEM & BIOCHEM,BOULDER,CO 80301
[2] RIBOZYME PHARMACEUT INC,DEPT CELL BIOL & ENZYMOL,BOULDER,CO 80301
关键词
D O I
10.1074/jbc.270.43.25702
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
A systematic study of selectively modified, 36-mer hammerhead ribozymes has resulted in the identification of a generic, catalytically active and nuclease stable ribozyme motif containing 5 ribose residues, 29-30 2'-O-Me nucleotides, 1-2 other 2'-modified nucleotides at positions U4 and U7, and a 3'-3'-linked nucleotide ''cap.'' Eight 2'-modified uridine residues were introduced at positions U4 and/or U7. From the resulting set of ribozymes, several have almost wild-type catalytic activity and significantly improved stability. Specifically, ribozymes containing 2'-NH2 substitutions at U4 and U7, or 2'-C-allyl substitutions at U4, retain most of their catalytic activity when compared to the all-RNA parent. Their serum half-lives were 5-8 h in a variety of biological fluids, including human serum, while the all-RNA parent ribozyme exhibits a stability half-life of only similar to 0.1 min. The addition of a 3'-3'-linked nucleotide ''cap'' (inverted T) did not affect catalysis but increased the serum half-lives of these two ribozymes to >260 h at nanomolar concentrations. This represents an overall increase in stability/activity of 53,000-80,000-fold compared to the all-RNA parent ribozyme.
引用
收藏
页码:25702 / 25708
页数:7
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