Background

Hammerhead ribozymes were discovered as self-cleaving motifs in a number of small, circular, pathogenic RNAs in plants [1–3]. Uhlenbeck [4] showed that the ribozyme was able to act in a bimolecular fashion as a true enzyme, ie each ribozyme was able to cleave multiple substrates. Haseloff and Gerlach [5] divided the hammerhead into a form in which the majority of the conserved nucleotides were located on the enzyme strand, with the only sequence requirements for the substrate being UH (H = A, U or C) [6–8]. Since 1988 this configuration, as shown in Figure 1, has been the paradigm for hammerhead ribozyme design. Hammerhead ribozymes are sequence-specific RNA cleaving agents with the potential to control the expression of genes by eliminating specific RNAs. This can be achieved by expressing the ribozyme within the target cell or by delivering it to the cell as a preformed entity. One of the difficulties associated with delivering preformed ribozymes is their instability in vivo, since RNA is degraded very rapidly by ribonucleases present in cells and extracellular fluids. Significant segments of ribonucleotides in the hammerhead ribozyme can be replaced with more nuclease-resistant analogues like DNA, phosphorothioate linkages, or 2' O-methyl analogues; however, within the conserved core of the hammerhead, the majority of ribonucleotides are sensitive to modification. Yang et al [9] demonstrated that predominantly DNA ribozyme analogues with at least 4 ribonucleotides (G5, G8, A9 and A15.1 or G15.2 numbered according to [10]) displayed measurable cleavage activity (albeit reduced 5000-fold). Phosphorothioate modification of DNA hybridising arms and three of the conserved pyrimidines (C3, U4 & U7) resulted in significant increase in stability in human serum with a 6-fold loss in cleavage activity [11]. In the context of 2'-O-methyl substituted ribozyme analogues, at least 5 unmodified ribonucleotides (G5, G8, A9, A15.1 and G15.2) were required for activity [9]. Paolella et al [12] identified a minimum set of 6 ribonucleotides, U4, G5, A6, G8, G12 and A15.1, in the conserved domain in which substitution with 2' O-allyl ribonucleotides inhibited activity. Eckstein's group [13, 14] showed that good activity and stability in foetal calf serum could be achieved with 2'-amino-2'-deoxyuridines at U4 and U7, and 2'-fluoro-2'-deoxycytidine at C3. Hammerheads in which helix II was shortened to only two base pairs, and all the pyrimidines were 2'-fluoro or 2'-methoxyethoxy derivatives except for U4 and U7 which were 2'-amino-2'-deoxy, were only 2–3 fold less active than the unmodified parent hammerhead [15], but showed a 104-fold increase in nuclease stability. A study of the effects of various modified nucleotides on stability and activity of the 2'-O-methyl-pyrimidine modified hammerhead found a number of modifications, including 2'-amino-2'-deoxyuridine, 2'-O-methyl-uridine, and 2'-C-allyl-uridine at positions U4 and U7, supported good rates of cleavage [16]. These modifications result in a greater than 103-fold increase in stability in human serum, while the addition of an inverted thymidine at the 3' end of the oligonucleotide (a 3'-3' linkage) further improved the stability by two orders of magnitude.

Figure 1
figure 1

Schematic representation of Mrz-12/12-A bound to substrate S-30. Helices I and III are formed between the ribozyme and substrate. The standard hammerhead (eg Rz-12/12) has a 4 base pair helix II in place of the single g-c pair in the miniribozyme. The minizyme (Mz-12/12) has no helix II, but has a loop sequence gtttt connecting bases A9 and G12. Upper-case letters represent ribonucleotides, and lower-case letters represent deoxyribonucleotides. Nucleotides which have been further modified in this study are shown in blue.

Full size image

Our laboratory is interested in the relationship between hammerhead design and reactivity. We have described a number of ribozyme derivatives that appear to have promise as RNA cleavage agents. Minizymes (Mz) possess a non-base-pairing tetranucleotide linker in place of helix II [17]. In general, such minizymes are less active than standard hammerheads, although in some instances they show comparable cleavage rate constants [18, 19]. Miniribozymes (Mrz) have a single G10.1–C11.1 base pair joined by a flexible linker in place of helix-loop II [19]. Asymmetric hammerheads are those in which the 5' hybridising arm is restricted to around 5 or 6 nucleotides; this modification eliminates the decrease in cleavage rate that occurs with standard hammerheads when the length of helix I, formed upon binding the substrate, increases to greater than about 6 base pairs [20, 21]. The purpose of this study was to investigate the ability of these various derivatives to cleave an RNA molecule (sequence derived from the mRNA of the cpsII gene of the Malaria-causing organism Plasmodium falciparum [22]) in the context of two substrates, a 30-mer and a 550-mer. Having optimised the cleavage activity of the ribozyme, we planned to chemically modify the nuclease sensitive RNA nucleotides, using readily available protected nucleoside phosphoramidites, to extend the life of the ribozyme in the presence of human serum.

Results

Ribozyme design

The primary target site for cleavage in this study was a previously identified site [23] in the cps II mRNA [22] of Plasmodium falciparum. The chosen target site, centred at position 3733 in the nucleotide sequence (Genbank reference L32150), has the local sequence 5' UAA CUU AUC AAG GUC* AAG AAC AUG AUG UUC 3', where the site of cleavage is denoted by the asterisk. A number of ribozyme designs were tested for their ability to cleave this RNA sequence either as a short (30-mer) oligonucleotide or in a transcribed RNA segment (550 nt). These designs included standard hammerhead ribozymes (Rz) which are defined as those with a helix II consisting of four base pairs closed at the end with a four-nucleotide loop, minizymes (Mz) [17] which lack helix II and instead the two segments of conserved nucleotides are linked between A9 and G12 with a non-base-paired linker (in this case consisting of 5 nucleotides), and finally miniribozymes (Mrz) [19] which have a single G-C base pair replacing helix II and in this instance a linker sequence consisting of four deoxythymidines. In this communication the core of each ribozyme is flanked by hybridising arms composed of DNA of various lengths, where the length is given in the ribozyme's name (e.g. Rz-6/12 has 6 nt in its 5' hybridising arm and 12 nt in its 3' arm). Hammerhead-ribozyme derivatives of these designs were tested for their ability to cleave the 30-mer substrate at pH 7.6, 37°C and 10 mM MgCl2 under pseudo first-order conditions with an excess of ribozyme. Ribozyme concentrations ranged from 50 nM to 10 μM. Cleavage data fitted well to single exponential curves to yield observed rate constants which were plotted against the ribozyme concentration in each experiment to determine the apparent dissociation constant ("Kd") and the maximum cleavage rate constant (kmax) for each ribozyme-substrate pair (Table 1). In terms of catalytic efficiency, the most efficient ribozyme was the standard hammerhead Rz-12/12. Its efficiency is due to a very low "Kd" of 7 nM, despite displaying a kmax some 5-fold less than Mrz-12/12. The highest kmax was displayed by Rz-6/12; however it had a "Kd" about 60-fold greater than Rz-12/12.

Table 1 Kinetic parameters for RNA/DNA unmodified hammerhead ribozyme derivatives.
Full size table

The abilities of all the ribozymes to cleave the same target in the context of transcribed RNA (550 nt) was also examined. Mrz-12/12, by virtue of only a modest decrease in kmax, and marginal increase in "Kd", was by far the most efficient of all the designs tested. In contrast Mrz-8/8, Rz-12/12 and Rz-6/12 displayed "Kd"'s between 2 and 3 mM, which, in the case of Rz-12/12, is an increase of about 400-fold. Interestingly the kmax values displayed by Rz-12/12 and Rz-6/12 were within experimental error, and were the same as displayed by Rz-12/12 for cleavage of the short substrate.

Cleavage of other targets by the miniribozyme

We examined whether the effectiveness of the miniribozyme design was limited to this target site. Miniribozymes, with long (>10 nucleotides) hybridising arms were designed to cleave RNAs of interest to other projects in the laboratory. Tet Mrz was a 53-mer oligonucleotide with conserved bases of RNA and hybridising arms and stem loop II composed of DNA. This Mrz, with hybridising arms of 18 and 19 nucleotides, was targeted to cleave the GUC triplet at position 60 of the Tetrahymena IVS ribozyme [24]. It cleaved the 388-nt transcript, L-21 ScaI, with a rate constant of 4.0 ± 0.2 min-1 (t1/2 = 10 seconds), to about 70%, at pH 7.6, 37°C and 10 mM MgCl2. Another miniribozyme with 14-mer arms (HC Mrz), targeting a segment of Hepatitis C polyprotein mRNA, was tested against a synthetic 29-mer substrate. Under our standard conditions about 70% of the substrate was cleaved, and the cleavage rate (>5 min-1) was too fast to be measured reliably. In contrast, the standard ribozyme HC Rz cleaved 78% of the same substrate with a rate constant of only 0.2 ± 0.02 min-1. Finally, PDGF MRz, with hybridising arms each of 10 ribonucleotides, was tested against both 25-mer synthetic and 707-nt transcribed substrates. Under standard conditions, the 25-mer was ~ 80% cleaved with a rate constant > 5 min-1. Reducing the magnesium ion concentration to 1 mM yielded a rate constant of 2.8 min-1 and 63% cleavage for the 25-mer substrate, and 1.6 min-1 and 45% cleavage for the 707-nt transcript.

Identification of nuclease susceptible sites in human serum

Mrz-12/12 was the most efficient cleaver of the 550-nt cpsII RNA transcript and was used as the platform to test the effect of chemical modification on cleavage activity and nuclease stability. Firstly, the stability of unprotected Mrz-12/12 in RPMI + 10% human serum was determined using 32P 5'-end labelled ribozyme at 37°C (Figure 2). Approximately 90% of the miniribozyme is degraded in 10 seconds, and no full-length material is observed after 10 minutes. Initially there are three main sites of cleavage, at U4, U7 and C15.2. After 10 minutes, nearly all the end-labelled material co-migrates with the band generated by alkaline digestion at U4. That initial, major product has a half-life of about two hours under these conditions, as it is slowly converted to a product one nucleotide shorter, ie its 3' end corresponds to C3 in the original miniribozyme.

Figure 2
figure 2

Degradation of 5' end-labelled Mrz-12/12 A in RPMI + 10% human serum at 37°C. Time of incubation in indicated above each lane. OH-indicates an alkaline digest of the same material. FL indicates the position of the full-length miniribozyme. The position of the fragments terminating at each of the ribonucleotides is indicated by the letters adjacent to the alkaline digest.

Full size image

Nuclease resistant modifications

Commercially available modified phosphoramidites were used to generate hammerhead derivatives which were expected to be protected from nuclease degradation. The effect of the various modifications on the cleavage ability are given in Table 2. In these experiments the concentration of the miniribozyme was fixed at 1 μM and the substrate S-30 at 5 nM. The nucleotide most sensitive to chemical modification was U4. All the 2' modifications tested (amino, deoxythymidine, deoxyuridine, and O-methyl, shown as D, F, G and H, respectively, in Table 2) diminished activity by more than 10-fold. Only the presence of a phosphorothioate linkage between U4 and G5 preserved the activity of the unmodified ribozyme. The ready availability of 2'-O-methyl phosphoramidites, coupled with the previous demonstrations [9, 16] of tolerance to that modification at C3, U7 and C15.2, lead us to synthesise Mrz-J, which we expected to have reasonable activity and nuclease stability. Its cleavage rate constant was actually twice that observed for the unmodified ribozyme, and its stability in serum was increased about 103-fold. The kinetics of degradation in serum (Figure 3) were not straight-forward, displaying a rapid initial decay of about 25% of the starting material, followed by an approximately first-order decay with a half-life around 30 minutes. This second phase accounted for approximately 50% in the total starting material, ie after about 4 hours approximately 25% of the full-length material remained intact and thereafter decayed only very slowly. There was a single major product, corresponding to cleavage at U4, observed over the six hours of the experiment.

Table 2 Cleavage Rate constants for cleavage of S-30 by Chemically Modified Mrz-12/12.
Full size table
Figure 3
figure 3

Degradation of Mrz-12/12 J in RPMI + 10% Human Serum. Experimental conditions are as described in Figure 2.

Full size image

The single degradation site in Mrz-J suggested that a more robust modification at this position would have a significant effect on its lifetime in serum. Mrz-12/12 K was synthesised with a 2'-amino modification at the U4 position and with a 2'-O-methyl modification at each of the three other conserved pyrimidines. Protection of the 3' end was omitted from Mrz-12/12 K because it did not appear to contribute significantly to the stability observed in Mrz-12/12 J. As expected, the cleavage activity of Mrz-12/12 K was significantly reduced compared to Mrz-12/12 J (Table 2), but stability in serum was greatly improved with only minor losses apparent after 5 hours incubation at 37°C (Figure 4). Even after 24 hours in 10% serum, approximately 25% of the radioactivity co-migrated with the full-length material, representing an almost 104-fold increase in stability. Even in the absence of 3' terminal protection there was no 3' exonuclease activity apparent. The amount of 32P label appearing in the gel lanes remained relatively constant throughout the experiment implying a lack of significant phosphatase activity in the serum. The main sites for degradation were the remaining unprotected (purine) ribonucleotides.

Figure 4
figure 4

Degradation of Mrz-12/12 K in RPMI + 10% Human Serum, and by alkaline digest. Experimental conditions are as described in Figure 2.

Full size image

The modifications to the conserved nucleotides in this study were all made in the context of a miniribozyme. Compared to a standard hammerhead, the catalytic domain is expected to be more conformationally flexible, and therefore it should not be assumed that all the changes described here can be directly applied to standard hammerheads with a helix II of four base-pairs. However, as for the miniribozyme, a standard ribozyme containing a 2'-amino modification at U4, was about 15-fold less efficient at cleaving S-30, (kobs = 0.05 min-1, Rz-12/12-L, Table 2), compared to the unmodified ribozyme (Rz-12/12).

Discussion

Work in this laboratory [20, 21] and elsewhere [25] has demonstrated that the cleavage kinetics of any conventional hammerhead ribozyme are significantly inhibited when the length of helix I exceeds about 6 bp. This has been ascribed to an interaction between helices I and II which stabilises an inactive conformation [20]. The angle between helices I and II changes with metal ion concentration [26], and we postulated that a similar change was required for the transformation between more and less active conformations of the ribozyme [20]. This general model is supported by more recent observations using a variety of techniques [27–31] which conclude that the dominant ground-state conformation of the hammerhead is inactive and is in equilibrium with the active form. The results of the present study are in accord with these conclusions.

It is commonly observed, for conventional hammerhead ribozymes, that cleavage efficiencies for long transcripts are about 2 orders of magnitude lower than for short substrates [32]. This has been observed here also for ribozyme derivatives of both the conventional design and of the short-armed (8-nt) miniribozyme (Table 1). In these cases the cause appears to reside largely in the apparent dissociation constant "Kd". In contrast, the longer-armed miniribozyme (Mrz-12/12) shows excellent cleavage kinetics against both short and long substrates. It appears that the more flexible miniribozyme is better suited to binding to the target in the context of a long RNA. These data can be interpreted according to a simple model in which ribozymes possessing a stable helix II form a more rigid three-dimensional structure [33, 34] which does not bind strongly to the long, folded substrate. When binding is achieved at very high ribozyme concentrations, the ribozyme-substrate complex is sterically hindered to such an extent that the complex is locked into a poorly active conformation. Hence Rz-6/12 and Rz-12/12 display similar maximal rate constants. In contrast, the Mrz lacking helix II is more flexible and readily adapts to binding the folded substrate with relatively minor effects on kobs and "Kd". This observation is not specific to target or cleavage triplet, since four unrelated targets, including three long transcripts, one with an AUC cleavage triplet, were cleaved with rate constants much higher than typically reported for cleavage even of short substrates. It is worth noting the magnitude of the observed cleavage rate constants; under our standard conditions these miniribozymes cleave their targets with half-lives in the range of < 5 to 25 seconds.

The unmodified Mrz-12/12 was very unstable in 10% human serum. Degradation occurred by endonucleolytic cleavage at the 3' side of pyrimidine nucleotides. Since the hybridising arms and helix-loop II are composed of DNA, the four remaining ribo-pyrimidine nucleotides in the conserved domain were the critical residues for stabilisation. Modification of all four ribopyrimidines with 2'-aminouridine and 2'-fluorocytidine, (Mrz-12/12 B), resulted in a more than 10-fold decrease in maximum cleavage rate constant. This contrasts with some previous results where a U4, U7-amino derivatised ribozyme with a standard helix II was only marginally diminished in activity [14], and a U4, U7-amino derivatised ribozyme [16], in which all the remaining pyrimidines were modified with 2'-O-methyl groups, was only two-fold less active than the parent ribozyme. The study by Heidenreich et al [14] was confounded by the fact that the cleavage kinetics were measured against a long transcript and are relatively slow compared with rates typically observed for short substrates, and therefore it seems likely that access to the transcript, rather than chemistry of cleavage, may have been rate determining in that case. In a later report [15], a modification pattern identical to miniribozyme B (ie C3, C15.2-fluoro and U4, U7-amino) but in a ribozyme with a standard helix II resulted in a more than 10-fold loss in turnover number (kcat). The series of singly and doubly substituted miniribozymes (C-E) showed clearly that a 2'-aminouridine at position 4 was solely responsible for the loss in activity. This is consistent with the result of Beigelman et al [16], but, in contrast to that result, the cleavage activity of the miniribozyme was not rescued by the addition of an amino group at U7. A phosphorothioate linkage between U4 and G5 (Mrz-12/12 I) was the only modification tested here that did not suppress cleavage activity. This is in accord with interference studies [35, 36] identifying U4 as insensitive to phosphorothioate modification. The results for dU and 2'O-methyl substitutions contrast with Beigelman et al [16] where, in a background of 2'O-methyl-pyrimidines, the effect of those substitutions at U4 were relatively minor.

In serum, Mrz-12/12 J was degraded by cleavage at the U4 phosphorothioate, where an initial, quite rapid degradation was followed by a slower step which is not complete at 6 hours. Chemically synthesised phosphorothioate linkages are a mixture of two enantiomers and it is likely that the multiphase kinetics observed were due in part to the different susceptibility of the two isomers (Rp and Sp) to the nucleases present in the serum [37, 38]. Mrz12/12 K has 2'-amino modification at U4, is very stable in serum, and is only 7-fold less active than the unmodified parent. The products of nuclease cleavage of Mrz-12/12 K indicate that degradation occurred by cleavage at the unprotected ribopurine sites. This derivative was not protected at the 3' terminus, but unlike earlier work [11, 16, 38], there was no evidence in this experiment for 3'-DNA exonuclease activity.

In recent times RNAi has surplanted catalytic RNA as the method of choice for suppression of gene expression in many eukaryotic cells [39]. Results published to date suggest that it may be effective in many settings, including possibly as a therapeutic. However, the mechanistic details of RNAi activity are quite complex and are still being unravelled, and it seems likely that there will be cell types, perhaps whole classes of organisms, that lack the necessary cellular machinery. For this reason, it may be premature to abandon the autonomous catalytic RNAs. During the 1990's, many studies aiming to demonstrate hammerhead ribozymes as gene silencing agents in vivo were not successful. The results obtained here, and in other recent studies on the effect of non-conserved sequences on the kinetics of cleavage [25, 40, 41], are beginning to reveal shortcomings of many studies of that era. That is the in vivo catalytic efficiency of the hammerheads under study was compromised by their simplistic design, which was based on in vitro studies performed with very short substrates. We were too quick to ascribe poor cleavage of transcripts to "accessibility" issues, and too slow to undertake comprehensive studies to understand the phenomenon. The miniribozyme design, and the effective nuclease protection afforded by the simple chemical modifications described here, provide an opportunity to revisit cellular and in vivo experiments with hammerheads that are around two orders of magnitude more efficient.

Conclusions

Long RNA substrates are much more effectively cleaved by miniribozymes than similarly targeted standard hammerheads. The presence of a stable helix II in the standard hammerhead appears to inhibit binding of the ribozyme to the substrate, and prevent the conformational mobility required for activity. Miniribozymes are affected by serum nucleases in a similar way to standard hammerheads, with cleavage occurring at the 3' side of unprotected ribopyrimidines. This work shows that it is readily possible to modify RNA/DNA hammerhead ribozymes, using commercially available reagents, to yield greatly improved nuclease resistance and retention of significant cleavage activity. These modified miniribozymes represent excellent candidates for cellular and in vivo studies on suppression of gene expression.

Methods

Oligonucleotide synthesis

Oligoribonucleotides were synthesised using DNA phosphoramidites and ancillary reagents supplied by Perkin Elmer (Applied Biosystems Division, Foster City, CA), RNA and modified phosphoramidites from Glen Research (Sterling, VA) and using an Applied Biosystems Model 394 DNA synthesiser. Phosphorothioates were introduced by oxidation with Beaucage reagent (Glen Research, Sterling, VA). Deprotection and purification of oligonucleotides were as described previously [20]. The purity of each oligonucleotide was checked by labelling its 5'-end with 32P phosphate using T4 polynucleotide kinase (New England Biolabs, Beverly, MA, USA) and [γ-32P]-ATP (Du Pont, Wilmington, DE), followed by electrophoresis in a 15% polyacrylamide gel containing 7 M urea and visualisation using a Molecular Dynamics PhosphorImaging system (Sunnyvale, CA). The concentrations of the purified oligonucleotides were determined by UV spectroscopy using the following molar extinction coefficients for the various nucleotides at 260 nm: A, 15.4 × 103; G, 11.7 × 103; C, 7.3 × 103; T/U, 8.8 × 103 l mol-1 cm-1. All oligonucleotides were stored in distilled, deionised and autoclaved water at -20°C.

The 550-nt CPSII substrate was transcribed by T7 RNA polymerase from the vector pCPS3b.1 [22] after linearisation with Eco RI restriction enzyme using an Ampliscribe T7 kit (Epicentre Technologies, Madison, WI, USA). The transcription reaction contained CTP, GTP and ATP (unlabelled) at 5 mM, UTP at 0.5 mM and 32P UTP at about 1 nM. The transcription was for 90 minutes at 37°C, followed by the addition of 0.5 μL of DNAaseI and incubation for a further 20 minutes. The mixture was extracted three times with a 1:1 phenol/chloroform mix and once with chloroform, before precipitation of the transcript by the addition of 1/3 volume of 7.5 M ammonium acetate and incubation on ice for at least 2 hours. After recovery of the transcript by centrifugation and washing, the degree of incorporation of 32P-labelled uridine was measured by Cerenkov counting of the transcript and the unincorporated UTP. The Tetrahymena intervening sequence transcript was generated from the ScaI digested pT7L-21 vector [24] (ATCC 40291) using the same method. The PDGF transcript was generated by T3 RNA polymerase transcription from the Eco RI digested vector pBSPDGF-LA using an Ampliscribe T3 kit (Epicentre Technologies, Madison, WI, USA). The vector pBSPDGF-LA was generated by insertion of the Xba I/Eco RI fragment from pmetPDGF-LA [42] into a similarly digested pBluescribe vector.

Oligonucleotide sequences

Deoxyribonucleotides are denoted by lower case letters, ribonucleotides by uppercase letters, modified nucleotides are shown in bold, Cf= 2'-fluoro-2'-deoxycytidine, Cme= 2' O-methylcytidine, Uam= 2'-deoxy-2'-aminouridine, Ume= 2' O-methyluridine, ps = phosphorothioate linkage. S-30, UAA CUU AUC AAG GUC* AAG AAC AUG AUG UUc, * denotes site of cleavage; Mrz-8/8, atgttctt CUGAUGA gttttc GAAAC cttgat; Mrz-12/12, catcatgttctt CUGAUGA gttttc GAAAC cttgataagt; Mz-12/12 catcatgttctt CUGAUGA gtttt GAAAC cttgataagt; Rz-12/12, catcatgttctt CUGAUGA GUCC UUUU GGAC GAAAC cttgataagt; Rz-6/12, gttctt CUGAUGA GUCC UUUU GGAC GAAAC cttgataagt; Mrz-12/12-A (= Mrz-12/12), catcatgttctt CUGAUGA gttttc GAAAC cttgataagt; Mrz-12/12-B, catcatgttctt CfUamGAUamGA gttttc GAAACfcttgataagt; Mrz-12/12-C, catcatgttctt CUamGAUamGA gttttc GAAAC cttgataagt; Mrz-12/12-D, catcatgttctt CUamGAUGA gttttc GAAAC cttgataagt; Mrz-12/12-E, catcatgttctt CUGAUamGA gttttc GAAAC cttgataagt; Mrz-12/12-F, catcatgttctt CtGAUGA gttttc GAAAC cttgataagt; Mrz-12/12-G, catcatgttctt CuGAUGA gttttc GAAAC cttgataagt; Mrz-12/12-H, catcatgttctt CUmeGAUGA gttttc GAAAC cttgataagt; Mrz-12/12-I, catcatgttctt CUps GAUGA gttttc GAAAC cttgataagt; Mrz-12/12-J, catcatgttctt CmeUps GAUmeGA gttttc GAAACmecttgataagtps tps t; Mrz-12/12-K, catcatgttctt CmeUamGAUmeGA gttttc GAAACmecttgataagt; Rz-12/12-L, catcatgttctt CUamGAUGA GUCC UUUU GGAC GAAAC cttgataagt; Tet Mrz, gcaatctattggtttaaa CUGAUGA gttttc GAAAC tagctaccaggtgcatg 3'; HC Mrz, 5' gtcgccacgacgac CUGAUGA gttttc GAAAC gttcccgctggt 3'; HC Rz, 5' gtcgccacgacgac CUGAUGA GGCC GAAA GGCC GAAAC gttcccgctggt 3'; HC S29, 5' ACCAGCGGGAACGUCGUCGUCGUGGCGAc 3'; PDGF Mrz, 5' CAGCUUCCUC CUGAUGA ggtaac GAAAU GCUUCUCt 3' ; PDGF S25, 5' GAAGAGAAGCAUCGAGGAAGCUGUc 3'.

Cleavage kinetics

Cleavage kinetics were studied at 37°C, pH 7.6 and 10 mM MgCl2 under conditions of ribozyme excess; the substrate concentrations varied between 4 and 20 nM, and the ribozyme concentrations were between 20 nM and 10 μM. The short, synthetic substrates were labelled at their 5' ends using polynucleotide kinase (Roche Molecular Biochemicals) and γ-32P ATP. The long, transcribed substrates were uniformly labelled by including α-32P UTP in the transcription reaction. The ribozymes and 32P-labelled substrates were mixed together in 20 μL of 50 mM Tris buffer and heated to 85°C for two minutes, then incubated at 37°C for 2 minutes. The tube containing the mix was centrifuged, and 2 μL was removed and put into 4 μL quenching solution which contained 90% formamide, 20 mM EDTA and 0.01 % xylene cyanol and bromophenol blue. The reaction was initiated by the addition of 2 μL of 100 mM MgCl2, and 2 μL samples were removed at various times and quenched as described above. The reaction products were separated using 15% denaturing polyacrylamide gels (containing 7 M urea), and then imaged using a Molecular Dynamics PhosphorImager. At each time-point, the amount of the substrate cleaved was calculated and plotted versus time. The data were fitted by a least-squares method using the program MacCurveFit [43], to an equation of the form: Pt = P∞-(exp(-kobst)PΔ) where Pt is the amount of product at time t, P∞ is amount of product generated in the exponential phase of the reaction, kobs is the first-order rate constant for the reaction, and PΔ is the difference in the amount of product at t = 0 and P∞. Some reactions resulted in biphasic kinetics in which the first-order phase described above was followed by a slower step which was accommodated adequately in the curve-fitting process by the addition of a linear term, Pt = {P∞-(exp(-kobst)PΔ)} + d*t. Apparent dissociation constants "Kd" and the maximal first-order rate constants kmax were determined from the plot of kobs versus ribozyme concentration according to the simple binding isotherm: kmax = (kobs * [Rz])/("Kd" + [Rz]) by least-squares fitting using the program MacCurveFit.

Serum stability

Ribozymes labelled at their 5' end with 32P phosphate were dissolved in RPMI medium (Gibco) at 2 μM and the reactions were initiated by adding human serum (pooled human serum, Red Cross Blood Bank, Sydney, NSW), to a final concentration of 10%. A 2 μL sample was removed immediately and the remainder incubated at 37°C with samples removed at the times indicated in Figures 2,3,4. The samples were quenched by addition to 4 μL of 90% formamide containing 20 mM EDTA and 0.01% bromophenol blue and xylene cyanol. The products of nuclease digestion in each sample were separated on 15% polyacrylamide gels containing 7 M urea and imaged using a Molecular Dynamics PhosphorImager.