WO2008016473A2 - Dinucleotide mrna cap analogs - Google Patents

Abstract

Novel cap analogs which are easily synthesized, resulting in high levels of capping efficiency and transcription and improved translation efficiencies are provided. Such caps are methylated at the N7 position of one or both guanosines of the dinucleotide cap as well as at the 3' position on the ribose ring. Substituent groups on the ribose ring also result in the cap being incorporated in the forward orientation. Also provided are methods useful for preparing capped analogs and using mRNA species containing such analogs are also contemplated herein, as well as kits containing the novel cap analogs.

Description

DINUCLEOTIDE MRNA CAP ANALOGS

Cross-Reference to Related Applications

[0001] This application claims a priority benefit under 35 U.S.C. § 119(e) from U.S. Patent Application No. 60/820,771, filed July 28, 2006, which is incorporated herein by reference. Statement Regarding Federally Funded Sponsored Research or Development

[0002] Work described herein was funded at least in part by an SBIR grant (SBIR Phase II, No. R44GM070156-02) awarded by the National Institutes of Health. The U.S. Government may therefore have certain rights therein.

[0003] The section headings used herein are for organizational purposes only and should not be construed as limiting the subject matter described herein in any way.

Introduction

[0004] Eukaryotic mRNAs bear a "cap" structure at their 5'-termini that is well known to play an important role in translation. Naturally occurring cap structures consist of a 7-methyl guanosine that is linked via a triphosphate bridge to the 5 '-end of the first transcribed nucleotide, resulting in m⁷G(5')ppp(5')N, where N is any nucleotide. The mRNA cap plays an important role in gene expression. It protects the mRNAs from degradation by exonucleases, enables transport of RNAs from the nucleus to the cytoplasm, and participates in assembly of the translation initiation complex. nlOCS^pppCS^G (mCAP) has been used as the primer in transcription with T7 or SP6 RNA polymerase in vitro to obtain RNAs having a cap structure in their 5 '-termini. In vivo, the cap is added en2ymatically. However, over the past 20 years or so, numerous studies have required the synthesis of proteins in an in vitro translation extract supplemented with in vitro synthesized mRNA. The prevailing method for the in vitro synthesis of capped mRNA employs a preformed dinucleotide of the form m'GOOpppCS^G as an initiator of transcription. A disadvantage of using mCAP, a pseudosymmetrical dinucleotide, has always been the propensity of the 3'-OH of either the G or m⁷G (m⁷Guo) moiety to serve as the initiating nucleophile for transcriptional elongation. This leads to the synthesis of two isomeric RNAs of the form m7G(5')pppG(pN)_n and G(5')ppp7G(pN)_n, in approximately equal proportions, depending upon the ionic conditions of the transcription reaction. This may be problematic for various downstream processes, such as in vitro translation or crystallization studies. [0005] Unmethylated cap analog is a modified cap analog in which the methyl group on the guanosine is removed. The selective procedure for methylation of guanosine at N7 and 3' Omethylation and 5' diphosphate synthesis was established (Kore,A. and Parmar,G. Nucleosides, Nucleotides, and Nucleic Acids, 25:337-340, 2006 and Kore A.R., et al. Nucleosides Nucleotides Nucleic Acids 200625(3): 307-14. The Anti-Reverse Cap Analog (ARCA) is a modified cap analog in which the 3¹ OH group is replaced with OCH3. ARCA and triple-methylated cap analogs are incorporated in the forward orientation.

[0006] In the cell, the cap is added in the nucleus and is catalyzed by the enzyme guanylyl transferase. The addition of the cap to the 5' terminal end of RNA occurs after transcription but immediately after transcription initiation so that it is almost impossible to detect. The terminal nucleoside is always a guanine, and is in the reverse orientation to all the other nucleotides, i.e., 5 'Gppp5 'GpNpNp... and the cap contains two nucleotides, connected by a 5 '-5' triphosphate linkage.

[0007] Transcription of RNA usually starts with a nucleoside triphosphate (usually a purine, A or G). When transcription occurs in vitro, it typically includes a phage RNA polymerase such as T7, T3 or SP6, a DNA template containing a phage polymerase promoter, nucleotides (ATP, GTP, CTP and UTP) and a buffer containing magnesium salt. The synthesis of capped RNA includes the incorporation of a cap analog (e.g., N7 methyl GpppG or m7GpppG) in the transcription reaction. Excess m7GppρG to GTP (4:1) favors to increase the opportunity that each transcript will have a 5' cap. The mMESSAGE mMACMNE® kit from Ambion (Ambion, Inc., Austin, TX, a business of Applied Biosystems) recommends this ratio and will typically yield 80% capped RNA to 20% uncapped RNA, although total yields of total RNA are lower as GTP concentration becomes rate limiting as GTP is necessary for the elongation of the transcript.

[0008] The 5' cap structure enhances the translation of mRNA by helping to bind the eukaryotic ribosome and assuring recognition of the proper AUG initiator codon. This function may vary with the translation system and with the specific mRNA being synthesized. The consensus sequence 5'-GCCACCAUGG-3', also known as the "Kozak" sequence, is considered to be the strongest ribosomal binding signal in eukaryotic mRNA. For efficient translation initiation, the key elements are the G residue at the +1 position and the A residue at the -3 position.

[0009] During translation the cap is bound by translation initiation factor eEF-4E and the CBC recruits additional initiation factors. Decapping is catalyzed by proteins dcpl and dcp2 which compete with eIF-4E to bind to the cap. Translation results in amino acids as encoded by the mRNA to join together to form a peptide and occurs as three processes, initiation, elongation and termination. Initiation in eukaryotes involves attachment of a ribosome which scans the mRNA for the first methionine codon. Elongation proceeds with the successive addition of amino acids until a stop codon is reached, terminating translation.

[0010] Capped RNA encoding specific genes can be transfected into eukaryotic cells or microinjected into cells or embryos to study the effect of translated product in the cell or embryo. If uncapped RNA is used, the RNA in these experiments is rapidly degraded and the yield of translated protein is much reduced.

[0011] Isolated dendritic cells from a patient can be transfected with capped RNA encoding immunogen. The dendritic cells translate the capped RNA into a protein that induces an immune response against this protein. In a small human study, immunotherapy with dendritic cells loaded with CEA capped RNA was shown to be safe and feasible for pancreatic patients (Morse et al. Int. J. Gastroinstest. Cancer, 32:1-6, 2002). It was also noted that introducing a single capped RNA species into immature dendritic cells induced a specific T-cell response (Heiser et al. J. Clin. Invest., 109:409-417, 2002.

[0012] The recent literature reveals that chemical modification of m7Guo at either the 2' or 3' OH group results in the cap being incorporated solely in the forward orientation, even though the 2' OH group does not participate in the phosphodiester bond. This observation has prompted investigation of 2' and 3' OH modifications of m7Guo as well as modifications of m7Guo to create double- and triple-methylated cap analogs.

SUMMARY

[0013] A composition is provided comprising:

wherein A is selected from a halogen, OH, OCH₃, H, ter/-butyldimethylsilyl and 2',3'-O- isopropylidene, B is selected from a halogen, OH, OCH₃, NH₂, N₃, NO₂, CF₃, CHO, S, tert- butyldimethylsilyl, LNA, and 2',3'-0-isopropylidene; R] is CH₃ Or void, R₂ is selected from OH, OCH₃ and a halogen, n is 1, 2 or 3, and when B is OH or OCH_3> R₁ is void, and R₂ is OH₃ then A is neither OH nor OCH₃, and when A, B and R₂ are OH, Rj is not CH₃.

[0014] An anti-reverse cap analog composition is also provided which is represented by the formula:

wherein A is selected from a halogen, OH, OCH₃, H, terf-butyldimethylsilyl and 2 ',3'- O-isopropylidene, B is selected from a halogen, OH₅ OCH₃, NH_2, N_3, NO_2, CHO, S, tert- butyldimethylsilyl, LNA, and 2',3'-0-isopropylidene, Ri is void, R₂ is selected from OH, OCH₃ and a halogen, n is 1, 2 or 3; and when A is either OH or OCH₃, then R₂ is not OH.

[0015] A double-methylated cap analog composition is also provided as represented by the formula:

wherein A is selected from a halogen, OH, OCH₃, H,-and 2',3'-O-isopropylidene, B is selected from CF_3>OH, OCH₃, NH₂, N₃, NO₂, CHO₅ LNA₅ and 2',3'-0-isopropylidene, Ri is CH₃, R₂ is selected from OH₅ OCH₃ and a halogen, n is I₅ 2 or 3, and when A is OH, R₂ is not OH.

[0016] A triple-methylated cap analog is provided as represented by the formula:

wherein A is selected from OH and OCH3, B is selected from OH and OCH₃, and n is, I₅ 2 or 3.

[0017] When A or B are a halogen, the halogen can be fluorine, chlorine, bromine or iodine. The phophodiester linkage between the guanosine molecules can be a triphosphate linkage, a tetraphosphate linkage or a pentaphosphate linkage.

[0018] An RNA molecule is also provided which has incorporated at its 5' end one of the structures as described above.

[0019] Also provided is a kit for capping an RNA transcript comprising the formula: a) a cap analog have the structure as recited in claim 1 :

wherein a is selected from a halogen, OH, OCH₃, H, TBDMS and 2',3'-O- isopropylidene; B is selected from OH, OCH₃, NH_2, N₃, NO₂, CF_3, CHO, halogen, S, TBDMS₅ LNA, and 2',3'-0-isopropylidene; Ri is CH₃ or void; R₂ is selected from OH, OCThand a halogen; and n is, 1, 2 or 3; wherein when B is OH or OCH_3, and R₁ is void, A is neither OH nor OCH3 if R₂ is OH and b). RNA polymerase. The kit may also comprise nucleotides, ribonuclease inhibitor, enzyme buffer, and nucleotide buffer.

[0020] Also provided is a method of synthesizing a dinucleotide cap analog comprising: a) providing a first nucleoside comprising at least one of a 2' substituent and a 3' substituent on the ribose ring, b) phosphorylating the first nucleoside, forming a first nucleotide, c) methylating the first nucleotide, d) adding a phosphorylated second nucleotide optionally comprising a T ribose ring substituent, and e) linking said first nucleotide with said second nucleotide, forming a dinucleotide cap analog. .

[0021] These and other features of the present teachings are set forth herein.

BRIEF DESCRIPTION OF THE FIGURES

[0022] The skilled artisan will understand that the drawings, described below, are for illustration purposes only. The drawings are not intended to limit the scope of the present teachings in any way.

[0023] Figure 1 illustrates the synthesis scheme for novel double-methylated cap analogs.

[0024] Figure 2 illustrates the synthesis of a novel ARCA.

[0025] Figure 3 illustrates the basic RNA cap structure (mCAP) consisting of Pl- guanosine-5'-yl P3-7-methylguanosine-5'-yl triphosphate (m⁷G5'ppp5^!G).

[0026] Figure 4 illustrates exemplary modified cap analogs. Modifications are at either or both G7 positions and/or the 3' ribose position of the m⁷ Guo.

[0027] Figure 5 shows the results of digestion of AmbLuc poly A RNA with BIp 1

[0028] Figure 6 graphically depicts yields from transcription reactions by using double- and triple-methylated cap analogs in an AmbLuc poly A vector.

[0029] Figure 7 shows the high level of RNA integrity when capped as analyzed with an Agilent 2100 Bϊoanalyzer.

[0030] Figure 8 show the capping efficiency of RNA in a transcription reaction by a gel shift assay.

[0031] Figure 9 illustrates the comparison of protein expression between standard and ARCA, double-methylated, and triple-methylated capped luciferase RNAs with poly(A) tail at different time points after transfection.

[0032] Figure 10 illustrates transcript yield by using modified and normal cap analogs.

[0033] Figure 1 1 illustrates capping efficiency with fluorine-modified cap analogs

[0034] Figure 12 illustrates transfection efficiency of fluorine-modified cap analogs in a luciferase assay

DESCRIPTION OF VARIOUS EMBODIMENTS

[0035] For the purposes of interpreting this specification, the following definitions will apply and whenever appropriate, terms used in the singular will also include the plural and vice versa. In the event that any definition set forth below conflicts with the usage of that word in any other document, including any document incorporated herein by reference, the definition set forth below shall always control for purposes of interpreting this specification and its associated claims unless a contrary meaning is clearly intended (for example in interpreting the document where the term is originally used). The use of "or" herein means "and/or" unless stated otherwise or where the use of "and/or" is clearly inappropriate. The use of "a" herein means "one or more" unless stated otherwise or where the use of "one or more" is clearly inappropriate. The use of "comprise," "comprises," "comprising," "include," "includes," and "including" are interchangeable and not intended to be limiting.

[0036] As used throughout, "Me" is equivalent to "CH₃", "OCH₃" or "OMe" denotes an oxygen atom bound to a methyl group, "CHO" denotes a carbon atom, C, bonded to a hydrogen atom, H, and double-bonded to an oxygen atom, O, (O=CH-) and "Et" denotes "C₂H₅".

[0037] As used herein, the term "ARCA" or anti-reverse cap analog refers to a modified cap analog in which the 3' OH group is replaced with OCH3. The structure is represented as m₂ ⁷'^3'°(5')Gppp(5')G.

[0038] As used herein, the term "cap" refers to a non-extendible di-nucleotide that facilitates translation or localization, and/or prevents degradation of an RNAtranscript when incorporated at the 5' end of an RNA transcript, typically having an m7GpppG or m7GpppA structure. It consists in nature of the modified base 7-methylguanosine joined in the opposite orientation, 5' to 5' rather than 5' to 3', to the rest of the molecule via three phosphate groups i.e., Pl-guanosine-5'-yI P3-7-methylguanosine-5'-yl triphosphate (m⁷G5'ppp5'G).

[0039] As used herein, the term "cap analog" refers to a structural derivative of an RNA cap that may differ by as little as a single element.

[0040] As used herein, the term "double-methylated" cap (dm-CAP) refers to each guanosine molecule of a dinucleotide cap in which each N7 position contains a -CH₃ group. It is illustrated as m⁷ (5')Gppp(5')m⁷G.

[0041] As used herein, the term "triple-methylated" cap (tm-CAP) refers to the presence of a -CH₃ group on each N7 position of the guanosine molecules of a dinucleotide cap and an additional OCH₃ group in the 2' or 3' position of the ribose ring of one of the guanosine molecules. tmCAPs are illustrated as ni2⁷'² ° (5')Gppp(5')m⁷G, m₂ ⁷'³ ° (5')Gppp(5')m⁷G, m⁷(5')Gppp(5') m₂ ⁷'^2'0 G,or m⁷(5')Gppp(5') m₂ ^7l3'°-G.

[0042] As used herein, the term "enzymatically incorporatable" means that a nucleotide is capable of being enzymatically incorporated onto the terminus, e.g. 3¹ terminus, of a polynucleotide chain, or internally through nick-translation of a polynucleotide chain, through action of a template-dependent or template-independent polymerase enzyme. A nucleotide-5 '-triphosphate is an example of an enzymatically incorporatable nucleotide.

[0043] As used herein, the term "enzymatically extendable" or "3' extendable" means a nucleotide or polynuceotide that is capable of being appended to a nucleotide or polynucleotide by enzyme action. A polynucleotide containing a 3' hydroxyl group is an example of an enzymatically extendable polynucleotide.

[0044] As used herein, the term "halogen" refers to nonmetal elements of Group 7A of the Periodic Table of the Elemnts comprising fluorine, F, chlorine, Cl, bromine, Br, iodine, I, and astatine, At. Halogens are monovalent, readily form negative ions and occur as compounds or ions.

[0045] As used herein, the term "locked nucleic acid" (LNA) refers to a bridge between the 2'0 and 4'C methylene bicyclonucleotide monomers.

[0046] As used herein, the term "nucleobase" refers to a nitrogen containing heterocyclic moiety nucleobase. Non-limiting examples of suitable nucleobases include: adenine, cytosine, guanine, thymine, uracil, 5-propynyl-uracil, 2-thio-5-propynyl -uracil, 5- methylcytosine, pseudoisocytosine, 2-thiouracil, 2-thiothymine, 2-aminopurine, N9-(2- amino-6-chloropurine), N9-(2,6-diaminopurine), hypoxanthine, N9-(7-deaza-guanine), N9- (7-deaza-8-aza-guanine) and N8-(8-aza-7-deazaadenine).

[0047] As used herein, the term "nucleoside" refers to a compound consisting of a nucleobase linked to the C-I ' carbon of a ribose sugar or analog thereof. The ribose or analog may be substituted or unsubstituted. Substituted ribose sugars include, but are not limited to, those riboses in which one or more of the carbon atoms, preferably the 3'-carbon atom, is substituted with one or more of the same or different substituents such as -R, -OR, -NRR or halogen (e.g., fluoro, chloro, bromo, or iodo), where each R group is independently -H, Ci-C₆ alkyl or C3-C14 aryl. Particularly, riboses are ribose, T- deoxyribose, 2',3'-dideoxyribose, 3'-haloribose (such as 3'-fluororibose or 3'-chlororibose) and 3'-alkylribose. Typically, when the nucleobase is A or G, the ribose sugar is attached to the N⁹-position of the nucleobase. When the nucleobase is C, T or U, the pentose sugar is attached to the N'-position of the nucleobase (Kornberg and Baker, DNA Replication, 2^nd Ed., Freeman, San Francisco, CA, (1992)). Examples of ribose analogs include arabinose, 2'-O-methyl ribose, and locked nucleoside analogs (e.g., WO 99/14226), for example, although many other analogs are also known in the art.

[0048] As used herein, the term "nucleotide" refers to a phosphate ester of a nucleoside as a monomer unit or within a polynucleotide.

[0049] As used herein, the term "nucleotide triphosphate" refers to a nucleotide with a triphosphate ester group at the 5' position.

[0050] As used herein, nucleosides and/or nucleotides of the present teachings can comprise "natural sugars" (i.e., -ribose, 2'-deoxyribose, and the like) or sugar analogues.

[0051] As used herein, the term "sugar analog" refers to analogs of the sugar ribose. Exemplary ribose sugar analogs include, but are not limited to, substituted or unsubstituted furanoses having more or fewer than 5 ring atoms, e.g., erythroses and hexoses and substituted or unsubstituted 3-6 carbon acyclic sugars. Typical substituted furanoses and acyclic sugars are those in which one or more of the carbon atoms are substituted with one or more of the same or different -R, -OR, -NRR or halogen groups, where each R is independently -H, (Ci-Cβ) alkyl or (C₁-Ci₄) aryl. Examples of substituted furanoses having 5 ring atoms include but are not limited to 2'-deoxyribose, 2'-(Ci-C₆)alkylribose, 2' -(C₁- C_όJalkoxyribose, 2'-(C₅-Ci₄)aryloxyribose, 2',3'-dideoxyribose, 2',3'-didehydroribose_J 2'-deoxy-3'-haloribose, 2'-deoxy-3'-fluororibose, 2'-deoxy-3'-chlororibose, 2'-deoxy- 3'-aminoribose, 2'-deoxy-3'-(Ci-C₆)alkylribose, 2'-deoxy-3'-(Ci-C₆)alkoxyribose, 2'-deoxy-3'-(C₅-Ci₄)aryloxyribose, 3'-(Ci-C₆)alkylribose-5'-triphosphate, 2'-deoxy-3'-(Ci- C₆)alkylribose-5'-triphosphate.2'-deoxy-3'-(Ci -C₆)alkoxyribose-5 '-triphosphate, T- deoxy~3'-(Cs-C]₄)aryloxyribose-5'-triphosphate, 2'-deoxy-3'-haloribose-5'-rriphosphate, 2'-deoxy-3'-aminoribose-5'-triphosphate, 2',3'-dideoxyribose-5'-triphosphate or 2',3'-didehydroribose-5'-triphosphate. Further sugar analogs also include so called locked nucleic acids (LNAs) having the structure

and those described in Wengel, et al. WO 99/14226, incorporated herein by reference.

[0052] As used herein, the terms "polynucleotide", "oligonucleotide" and "nucleic acid' are used interchangeably and refer to single stranded and double stranded polymers of nucleotide monomers, including ribonucleotides (RNA) and 2'-deoxyribonucleotides (DNA) linked by internucleotide phosphodiester bond linkages. A polynucleotide may be composed entirely of deoxyribonucleotides, entirely of ribonucleotides or chimeric mixtures thereof.

[0053] As used herein, the term "terminator" means an enzymatically incorporatable nucleotide which prevents subsequent incorporation of nucleotides to the resulting polynucleotide chain and thereby halts polymerase-mediated extension. Typical terminators lack a 3'-hydroxyl substituent and include 2',3'-dideoxyribose, 2\,3'-didehydroribose, and 2',3'- dideoxy-3'-haloribose₅ e.g.3'-deoxy-3'-fluoro-ribose or 2',3'-dideoxy-3^r-fluororibose, for example. Alternatively, a ribofuranose analog can be used, such as 2',3'-dideoxy-β-D- ribofuranosyl, β-D-arabinofuranosyl, 3'-deoxy-β-D-arabinofuranosyl, 3'-amino-2',3'- dideoxy-β-D-ribofuranosyl, and 2',3'-dideoxy-3'-fluoro-β-D-ribofuranosyl (see, for example, Chidgeavadze et al., Nucleic Acids Res., 12: 1671-1686 (1984), and Chidgeavadze et al. FEB. Lett., 183: 275-278 (1985)). Nucleotide terminators also include reversible nucleotide terminators (Metzker et al. Nucleic Acids Res., 22(20):4259 (1994)).

[0054] As used herein, the term "nonextendable" or "3¹ nonextendable" refers to the fact that a terminator is incapable, or substantially incapable, of being extended in the 3' direction by a template -dependent DNA or RNA polymerase.

[0055] As used herein, the term "TBDMS refers to /ert-butyldimethylsilyl.

[0056] As used herein, the term "void" refers to the absence of a substituent group at the Ri position of the cap analog. The lack of a substituent group results in no positive chare o the imidazole ring. In one embodiment the substituent group may be a CH₃ group. When the CH₃ group is present, there is a positive charge on the imidazole ring.

[0057] Cap analog is used for the synthesis of 5' capped RNA molecules in in vitro transcription reactions. Substitution of cap analog for a portion of the GTP in a transcription reaction results in the incorporation of the cap structure into a corresponding fraction of the transcripts. Capped mRNAs are generally translated more efficiently in reticulocyte lysate and wheat germ in vitro translation systems. It is important that in vitro transcripts be capped for microinjection experiments because uncapped mRNAs are rapidly degraded. Cap analogs are also used as a highly specific inhibitor of the initiation step of protein synthesis.

[0058] In one embodiement novel ARCA, double- and triple-methylated cap analogs are disclosed. The cap structures have been synthesized and designed to attach in the forward orientation, i.e., 5'Gppp5'GpNpNp.... The resulting novel cap analogs have been demonstrated to improve the yield and efficiency of transcription compared to the standard cap analog as shown in Figures 6, 8, and 10.

[0059] These analogs also have novel substituent groups at the 2' and/or 3' positions of the ribose ring which also resulting in attaching of the cap in the forward orientation. In one embodiement, fluorine attached at the 2' or 3' position of the ribose.ring has been shown to improve both capping efficiency and translation efficiency as shown in Figures 11 and 12.

[0060] The synthesis of capped RNA which is not only efficiently capped and yields high levels of transcribed RNA is an area of unmet need. One approach which is being used by Ambion is disclosed in US patent application 2005/0287539, incorporated herein by reference. The synthesis of cap analogs which incorporate in only the forward orientation will improve transcription and translation efficiency.

[0061] The teachings of Darynkiewicz et al. in US Patent No. 7,074,596 have attemped to present synthesis methods and methylation methods for anti-reverse cap analogs. The method of methylation as taught was not reproducible in our hands, neither was the synthesis of a linker and methods for linking the nucleotides.

[0062] Thus, there exists in the art an unmet need for high yield transcription reactions that efficiently synthesize RNA. The resulting RNA finds use in a variety of applications, including ribozyme, antisense and biophysical studies, and gene array analysis. Additionally, capped RNA transcripts are used for applications requiring protein synthesis such as in vivo expression (e.g., microinjection, transfection and infection experiments) and in vitro translation.

[0063] In order to overcome the problem of synthetic mCAP attaching to RNA in the reverse orientation around 50% of the time, when NTPs and cap RNA are present in comparable concentrations, the present application teaches chemically convenient and reproducible methods for the synthesis of modified cap analog, anti-reverse cap analog (ARCA), and double- and triple- methylated cap analogues (Figures 1 and 2). [0064] The design and synthesis of novel cap analogs such as m7,2'FG[5']ppp[5']G and m7,2TG[5']ppp[5']m7G, a double-methylated cap, in which various moieties at the 2' and 3' positions on the ribose ring have been substituted are presented (Figure 2).

[0065] Also discovered and synthesized are triple-methylated caps. Such caps include m27,2'OG[5^I]ppp[5^I]m7G, m27,2OG[5']ppp[5'] m2'OG₅ m27₅3'OG[5^l]ppp[5^I]m7G, and m27₅2OG[5']ppp[5'] m27,2'OG. Additionally, details of the compatibility of new, modified cap analogs with respect to transcription, capping and translation efficiency by using HeLa cells in comparison with the standard and conventional ARCA cap analog is presented.

[0066] Structures were confirmed by ¹H NMR and ³¹P NMR. Transcripts produced with T7 RNA polymerases using "anti-reverse" cap analogs (ARCAs) were of the predicted length and indistinguishable in size and homogeneity from those produced with m⁷GpppG. Transfection assays were performed by using standard cap analog-capped and ARCA- capped luciferase in in vitro transcribed RNA with HeLa cells. Finally, luciferase activity was measured and revealed that ARCA-capped transcripts were 2.2 to 2.5 fold higher than that of m⁷GpppG-capped transcripts. This finding also suggest that the presence of reverse caps in conventional in v/ϊro-synthesized mRNA reduces their translation efficiency.

[0067] Those having ordinary skill in the art will understand that many modifications, alternatives, and equivalents are possible.

[0068] All such modifications,- alternatives, and equivalents are intended to be encompassed herein.

MATERIALS AND METHODS Reagents

[0100] AU of the reagents and solvents are used as such without further purification, unless otherwise stated. Guanosine 5 '-diphosphate, Dimethyl sulfate, anhydrous dimethylformamide , 2,2'-dithiodipyridine (Aldrithiol), Triphenylphosphine, trimethylphosphate ((OMe)₃P), phosphorous oxychloride, phosphorous pentoxide, orthophosphoric acid, anhydrous methylene chloride, dichloromethane, Tributylamine, anhydrous pyridine were purchased from Sigma-Aldrich Co. 3'-O-Me-Guanosine is available from Chemgene, Boston, MA. Imidazolide GMP, lmidazolide GDP, Imidazolide 2'F-GMP, Imidazolide 3'CF₃-GDP, Imidazolide m⁷GMP, IM tris(triethylammonium) phosphate, and tributylammonium orthophosphate were made as taught herein or in A. Kore, and G. Parmar, Synthetic Comm., 36:3393-3399, 2006, incorporated herein by reference in its entirety.

[0101] The cap analogs were analyzed by ¹H NMR and ³¹P NMR (Broker Avance), 400 MHz. ¹H was collected at 400.1446006 MHz and the ³¹P was collected at 161.9968531, both using a QNP probe. Mass Spectroscopy (i.e., Applied Biosystems/Sciex MDX API 150 model) and MALDI-TOF (Applied Biosystems Voyager DE-PRO model), and analytical HPLC (Aliance, Water's) was performed using Hypersil SAX columns, 5 μm, 250 X 4.6 mm (Altech).

EXAMPLES

[0102] Aspects of the present teachings may be further understood in light of the following examples, which should not be construed as limiting the scope of the present teachings in any way.

[0103] While the present teachings are described in conjunction with various embodiments, it is not intended that the present teachings be limited to such embiodiements. On the contrary, the present teachings encompass various alternatives, modifications, and equivalents, as will be appreciated by those of skill in the art.

EXAMPLE l

[0104] Synthesis of 7-Methyl Guanosine 5'-diphosphate In a clean, dry 2000 mL round bottom flask equipped with a stirring bar and under a stream of argon slowly dissolve dry and finely powdered guanosine 5 '-diphosphate (1), (10.0 g, 20.5 mmol), either in free acid or sodium as a counter ion form, in 200 mL water, adjusting pH to 4.0 with glacial acetic acid. Dimethyl sulfate (20 mL, 119.04 mmol) was then added over a period of one hour with constant stirring at room temperature and the reaction continued for an addition hour during which time a decrease in pH was observed but pH was kept between pH 3.8 to 4.0 by drop-wise addition of 10 mM NaOH and methylations was monitored by analytical HPLC for progress. Methylation was determined to be 98% complete within 2 h. After 2 h, the reaction mixture was extracted with CHCl3(3 X 200 mL) to remove unreacted excess dimethyl sulfate.

[0105] The resulting aqueous layer was further evaporated on a rotary evaporator to remove any chloroform traces, and then further diluted to 1.5 L with water and loaded on an anion exchange resin, i.e., DEAE Sepharosa fast flow packed in a BPG 100 column (Amersham GE, Piscataway, NJ, USA). BPG (biological process glass) 100 specification: 100/500 column (100 mm in diameter and 50 cm in height), packed with DEAE Sepharosa fast flow resin to the bed volume of 400 mm. The desired compound was eluted by using four bed volumes of gradient from 0 to 80% of 1 M TEAB buffer (triethyammonium bicarbonate), pH 7.5, at a flow rate of 100 mL/min, using AKTA purifier 100 FPLC (Amersham GE). At 45% TEAB buffer, 7-methylguanosine 5 '-diphosphate (m⁷GDP) was eluted as a large broad peak, with a strong ultraviolet absorbance at 254 run. The residual bicarbonate was removed by co-evaporating with methanol, 3 X 600 mL. The resulting residue was transferred to a centrifuge tube, and 8.9 g sodium perchlorate dissolved in 1.1 L acetone was added and cooled 2 h at 4⁰C. The resulting mixture was centrifuged and the supernatant liquid was discarded. The precipitate was ground with a new portion of acetone, cooled and centrifuged, repeating once. The precipitate was dried in a vacuum desiccator over P₂O₅. The resulting amorphous white powder was 7 methyl-guanosine 5'- diphosphate. Taken from Kore,A. and Parmar,G. Nucleosides, Nucleotides, and Nucleic Acids, 25:337-340, 2006, incorporated herein by reference in its entirety.

EXAMPLE 2 Synthesis of NucIeoside-5'-diphosphates

[0106] Although the following procedure illustrates synthesis of guanosine-5'- diphosphate, one of skill in the art would be able to use the procedure for the synthesis of adenosine-5' -diphosphate, uridine-5'-diphosphate, and cytidine-5'-diphosphate and analogs thereof. In a clean, dry 500 mL round bottom flask equipped with a stirring bar the triethylammonium salt of guanosine 5 '-monophosphate (10.0 g, 21.5 mmol) in anhydrous dimethylformamide (200 mL) was stirred together, triethylamine was added (2.4 mL, 142.8 mmol) and allowed to stir for 5 min, followed by the addition of Imidazole (5.86 g, 86.1 mmol), 2,2'-dithiodipyridine (7.4 g, 33.58 mmol), and triphenylphosphine (8.9 g, 33.9 mmol). Stirring was continued for 2 h at room temperature. The reaction was allowed to go to completion as determined by HPLC and then poured slowly into a mixture of sodium perchlorate (7 g) in acetone (1500 mL), and then cooled for 30 min. at 4⁰C. The reaction mixture was centrifuged, discarding the supernatant. Traces of imidazole and triphenylphosphine were removed by grinding the solid with a new portion of acetone (400 mL), cooling and again centrifuged, repeating once. The precipitate was dried in a vacuum oven over P₂O₅ at 24⁰C (30 mbar pressure). The ribonucleoside-5'-phosphoroimidazolide thus obtained was dissolved in dimethylforamide (200 mL), and a 1 M solution of tributylammonium orthophosphate in dimethylformamide (80 mL) was added drop-wise to the vigorously stirred mixture over a period of 30 min. Zinc chloride (2 g, 14.67 mmol) was added and the reaction mixture stirred at room temperature for 3 h. Completion of the reaction was monitored by HPLC. The reaction mixture was quenched with water (50 mL) and extracted with chloroform (3 X 200 mL), concentrated in a rotary evaporator and then purified by application to an anion exchange resin.

[0107] Purification by column chromatography was accomplished with a DEAE Sepharose fast flow resin packed in an XK 50/60 column (50 mm diameter and 60 cm long) (Amersham GE). The desired compound was eluted by using four bed volumes of gradient from 0 to 80% of 1 M TEAB buffer pH 7.5 (triethylammonium bicarbonate) at a 'flow rate of 20 mL/min, using an AKTA purifier 100 FPLC (Amersham GE). At 55% TEAB buffer, the desired product (nucleoside-5'-diphosphate) was eluted as a large broad peak, with a strong ultraviolet absorbance at 254 nm. The nucleoside-5'-diphosphate-containing fractions were pooled and evaporated using a rotary evaporator to give triethylamine salt of the desired diphosphate compound. Taken from A. Kore, and G. Parmar, Synthetic Comm., (2006) supra.

EXAMPLE 3

Synthesis of 3'-O-Methyl Guanosine Monophosphate (3'-0-Me-GMP) TEA Salt (Compound 2)

[0108] In a clean, dry 500 mL round bottom flask equipped with a stirring bar and under a stream of argon slowly add dry and finely powdered 3'-O-Me-Guanosine (1), (6 g, 20 mmol) to a mixture of trimethylphosphate ((OMe)₃P) (50 mL) and phosphorous oxychloride (POCI₃) (6 mL, 60 mmol) at O⁰C in small portions with continuous stirring under argon. The mixture was kept at 0 — 4⁰C and allowed to stir at least 19 hrs. Diethyl ether (200 mL) was added to extract the excess phosphorous oxychloride and to simultaneously precipitate the 3'-O-methylguanosine-5'-phosphodichloridate, which was then pelleted by centrifugation and dissolved in 100 mL ice-cold 5% NaHCO₃ in water. The resulting aqueous solution was adjusted to pH ~1.5 using 1 N NaOH. After stirring at 0 - 4 ⁰C for an additional 20 h, the pH was adjusted to 7.0 and the resulting mixture was applied to a column of DEAE Sephadex A25. The column was washed with 5 mM TEAB buffer, pH 7.5 and then eluted with freshly prepared IM Triethylammonium bicarbonate (TEAB) buffer, pH 7.5. Fractions containing the 3'-O-Me GMP TEA salt (2) were pooled, concentrated to dryness.

EXAMPLE 4 Synthesis of 3'-0-Me-GMP Imidazolide (Compound 3)

[0109] In a clean, dry 1 L round bottom flask equipped with a stirring bar and under a stream of argon slowly add anhydrous DMF (144 mL) and the triethylamine (0.933 mL, 9.23 mmol) allow to stir for at least 5 min. To this slowly was add the dry and finely powdered 3'-0-Me-GMP TEA salt (2), (3.5 g, 7.34 mmol) in small portions with continuous stirring under argon. Thereafter the Imidazole (2.05 g, 30.1 mmol), Aldrithiol (2.65 g, 12.02 mmol), and triphenylphosphine (3.13 g, 11.9 mmol) were added and the reaction allowed to stir at room temperature for at least 2-3 h, during which the reactants became soluble making the reaction appear clear yellow colored. Upon completion, sodium perchlorate (3.0 g, 24.5 mmol) dissolved in acetone with continuous stirring and to this mixture, slowly added, was the reaction mixture. This mixture was then poured in two IL nalgene bottles and cooled in a refrigerator at -8O⁰C for 30 minutes. The mixture was then subjected to centrifugation at 3000 rpm for 15 min and the supernatant was discarded. The precipitate was ground with a new portion of acetone and centrifuged. The process was repeated once more and the precipitate was dried in a vacuum desiccator over phosphorous pentoxide, yielding 3'-0-Me-GMP Imidazolide.

EXAMPLE 5 Synthesis of 3'0-Me-GDP TEA salt (Compound 4)

[0110] Synthesis of Tris(triethylammonium) phosphate linker:

Anhydrous orthophosphoric acid (22.5 g, 229.59 mmol) was added to 50 mL of anhydrous methylene chloride in a clean, oven dried 250 mL flask equipped with a stirring bar. Tributylamine (54.6 mL, 229.6 mmol) was then added into the solution drop wise through an addition funnel over a period of 30 min. The mixture was left stirring for 1 h. CH₂Cl₂ was then evaporated and the reaction residue was co-evaporated with 3 X 30 mL of anhydrous pyridine and then 2 X 30 mL of anhydrous DMF. The Tris(triethylammonium) phosphate linker product was dissolved in 100 mL anhydrous DMF so as to have a final concentration of 1 M, and stored over 4A molecular sieves at 4⁰C. [0111] In a clean, dry IL round bottom flask equipped with a stirring bar and under a stream of argon anhydrous DMF (40 mL) was slowly added and stirred for at least 5 minutes. To this was slowly added finely powdered 3'-0-Me-GMP Imidazolide (3), (3.0 g, 7.04 mmol) in small portions with continuous stirring under argon. Zinc chloride (2.0 g, 14.6 7 mmol) was added in small portions until the contents were dissolved. Thereafter, the tris(triethylammonium) phosphate linker andl M tributylammonium orthophosphate (40 mL) was added slowly to the reaction mixture under argon and the reaction was allowed to stir at room temperature for 5 h. The reaction when followed on HPLC showing complete conversion of the starting material, 3'-0-Me-GMP Imidazolide (3) to its corresponding diphosphate. Upon completion, the reaction was supplemented with water, 100 mL, and the resultant mixture was extracted with chloroform (3 X 250 mL), subjected to volume reduction (~100 mL) by evaporation and applied to DEAE Sephadex A25 column, eluting with a linear gradient of freshly prepared 1 M TEAB, pH 7.5. The fractions containing the pure 3'O-Me-GDP TEA salt (compound 4) were eluted, combined and evaporated to dryness.

EXAMPLE 6 Synthesis of m₂ ^7>3'⁰GDP (Compound 5)

[0112] To a stirred solution of 3'-0-Me-GDP TEA salt (4), (4.0 g, 6.1 mmol) in 100 mL of nuclease free water, concentrated glacial acetic acid was slowly added to adjust the pH of the solution to 4.0; dimethyl sulfate ((Me)₂SO₄) (20 mL, 210 mmol) was slowly added drop wise over a period of 60 min, while maintaining the pH~4.0-4.5 with 50 mM NaOH. The reaction was allowed to stir at room temperature for 2 h and methylation was > monitored by HPLC. After 2 h, the reaction mixture was extracted with CHCl₃ (3 X 250 mL) to remove unreacted dimethyl sulfate. The aqueous layer was applied to a DEAE Sephadex column and the fractions containing the product were pooled, evaporated and dried in a vacuum desiccator over phosphorous pentoxide to give 3'-O-Me (N⁷-Me) GDP (compound 5) as a fine powder.

EXAMPLE 7 Synthesis of m₂ ^{7l3 O}G[5']ppp[5']G (Compound 7)

[0113] In a clean, dry IL round bottom flask equipped with a stirring bar and under a stream of argon anhydrous DMF (165 mL) was slowly added and allowed to stir. To this was slowly add finely powdered 3'-0-Me-GDP TEA salt (5), (4.0 g, 5.84 mmol) in small portions with continuous stirring under argon. Zinc chloride (2.0 g, 14.67 mmol) was added in small portions until the contents were dissolved. Thereafter, the Imidazolide GMP (compound 6) (6.00 g, 14.08 mmol) was slowly added to the reaction mixture under argon. The reaction was allowed to stir at room temperature and methylation was monitored by HPLC. Upon complete disappearance of starting material, 3'-0-Me-GDP TEA salt, the reaction was poured into a solution of EDTA (3.0 g) in water (200 mL) and pH adjusted to 7.0 with saturated NaHCOs. This was then applied to a DEAE Sephadex column, eluted with a linear gradient of freshly prepared 1 M TEAB, pH 7.5 and the fractions containing the product were pooled, evaporated and dried to give pure 3'-O-Me-N7-Me-G[5']ppp[5']G (compound 7), stored at -2O⁰C.

EXAMPLE 8 Synthesis of m₂ ^7>3'oG[5']ppp[5']in⁷G (Compound 8)

,[0114] To a stirred solution of compound 7 (500 mg, 0.612 mmol) in 5.0 mL water, concentrated glacial acetic acid was added slowly to adjust the pH of the solution to 4.0 and to this mixture dimethyl sulfate (2.0 mL, 21.1 mmol) was slowly added drop-wise over a period of 60 min, while maintaining the at pH~4.0-4.5 with 50 mM NaOH. The reaction was allowed to stir at room temperature for 2 h and methylation was monitored by HPLC. After 2 h, the reaction mixture was extracted with CHC13 (3 X 50 mL) to remove unreacted dimethyl sulfate. The aqueous layer was applied to a DEAE Sephadex column and the fractions containing the product were pooled, evaporated and dried to give pure trimethylated CAP (m27,3OG[5']ppp[5']m7G ). (compound 8) which was then passed through a Strata AW column to remove the salt and make it a free acid form.

EXAMPLE 9 Synthesis of 2'F GMP (Compound 14):

[0115] To a stirred solution OfPOCl₃ (3.97 g, 26.3 mmol) and (OMe)₃P (20.0 mL) at O⁰C under nitrogen atmosphere, 2'-fluro guanosine (2.5 g, 8.77 mmol) was added and the reaction mixture was stirred for 2 h at O⁰C. After 2 h, 50.0 mL water was added to the reaction mixture. The resulting reaction mixture was washed with ethyl acetate (2 X 50 mL) to remove the phosphorylating agent. The collected aqueous solution was adjusted to pH 1.5 drop-wise with IN NaOH and allowed to stir at 4⁰C for 12 h. After 12 h, the aqueous solution was concentrated under a rotor evaporator to around 20 mL. To a solution of sodium perchlorate (3.0 g) in 100 mL acetone in a centrifuge tube at O⁰C this concentrated solution (20.0 mL) was added slowly for 2 minutes. The resulting mixture was centrifυged and the supernatant liquid was removed. This precipitate was dissolved in 500 mL water and adjusted the pH to 5.5 with saturated NaHCCb and loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0-lM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and dried in a vacuum desiccator over phosphorous pentoxide (P2O₅) to give 2'F GMP as a fine white powder (compound 14) (Yield: 3.54 g, 87%).

EXAMPLE 10 Synthesis of Imidazolide 2'F GMP (Im2'F GMP) (Compound 15):

[0116] To a stirred solution of 2¹F GMP TEA salt 14 (2.0 g, 4.3 mmol) in a 50 mL dry DMF₅ imidazole (1.50 g, 21.5 mmol), triphenyl phosphine (PPh₃) (2.26 g, 8.6 mmol), aldrithiol (1.90 g, 8.6 mmol) and triethylamine (0.43 g, 4.3 mmol) were added. The reaction mixture was stirred under nitrogen atmosphere at room temperature for 5 h. To a solution of sodium perchlorate (2.0 g) in 100 mL acetone in a centrifuge tube at 0⁰C, the above reaction mixture was added slowly for 5 minutes. The resulting mixture was centrifuged and the supernatant liquid was removed. The solid was ground with a new portion of acetone (100 mL), cooled, and centrifuged again. This process was repeated twice, and the resulting solid was dried in a vacuum desiccator over P₂O₅ to give Imidazolide 2¹F GMP as a white powder (compound 15) (Yield: 1.44 g, 81%).

EXAMPLE 11 Synthesis of 2'F GDP (Compound 16):

[0117] To a stirred solution of Imidazolide 2¹F GMP 15 (1.2 g, 2.89 mmol) and Zinc chloride (0.38 g, 2.89 mmol) in 10.0 mL dry DMF, 18 mL of IM tris(triethylammonium) phosphate (tris(Et₃NH)₃PO₄) in DMF was added under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 3 h. After 3 h, the reaction mixture was diluted with 50.0 mL of water. The resulting reaction mixture was washed with ethyl acetate (2 X 50 mL) to remove the phosphorylating agent. The collected aqueous solution was adjusted to pH 5.5 with saturated NaHCCb and loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and dried in vacuum desiccator over phosphorous pentoxide to give 2'F GDP as a fine white powder (compound 16) (Yield 134 g, 72%).

EXAMPLE 12 Synthesis of m⁷'^{2 ;r}GDP (Compound 17):

[0118] To a stirred solution of 2'F GDP 16 (0.75 g, 1.16 mmol) in 20.0 mL of water, acetic acid was added slowly to adjust the pH of the solution to 4.0. To this mixture, dimethyl sulfate (3.0 mL) was added drop-wise over a period of 30 min. and the reaction mixture was allowed to stir at room temperature for 4 h. As the methylation proceeds, the pH decreased to around pH 2.0 and was re-adjusted back to pH 4.0 using a IM NaOH solution. After 4h, the reaction mixture was extracted with CHC13 (3 X 50 mL) to remove unreacted, excess dimethyl sulfate. The collected aqueous solution was adjusted to pH 5.5 with saturated NaHCC>₃ and applied onto a DEAE Sephadex column. The final product was monitored for methylation by HPLC?? αn<i eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and dried in vacuum desiccator over phosphorous pentoxide to give m^7>2/rGDP as a fine white powder (compound 17) (Yield 0.64 g, 83%).

EXAMPLE 13 Synthesis of m^{7>2 f}GpppG (Compound 18):

[0119] To a stirred solution of m^GDP 17 (0.2 g, 0.3 mmol) and Imidazolide GMP (ImGMP) (0.19g, 0.45 mmol) in 10.0 mL dry DMF, Zinc chloride (81 mg, 0.6 mmol) was added under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 1 h. After 1 h, the reaction mixture was added to a solution of EDTA disodium (0.45 g, 1.2 mmol) in 100.0 mL of water at 0°C. The resulting aqueous solution was adjusted to pH 5.5 with saturated NaHCO₃ and loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and concentrated to 10.0 mL TEA salt of compound 18. The resulting 10.0 mL was passed through a Strata-X-AW column and washed with 10.0 mL water followed by 10.0 mL MeOH. Then, compound 18 was eluted with 15.0 mL OfNH₄OHTMeOHZH₂O (2/25/73) and the collected solution was evaporated and dried to give m^7>2VrGpppG as a fine white powder (compound 18) (Yield: 0.15 g, 58%).

[0120] HPLC Analysis: The starting imidzaolide gave a peak at 3.49 min. and the GDP peak was at 5.95 min. The new product peak was at 7.13 min. The crude reaction mixture after 1 h gave 97% of the product peak (7.14 min.) and 3% of the starting material peak (5.95 min.).

[0121] Data for 18. ¹H NMR (D₂0, 400 MHz) δ 8.02 (s, IH)₅ 6.14 (d, J= 14.4 Hz, IH), 5.80 (d, J= 5.6 Hz, IH), 5.41 - 5.27 (m, IH), 4.63 - 4.47 (m, 3H), 4.39 -4.24 (m, 6H), 4.03 (s, 3H); ³¹P NMR (D₂0, 162 MHz) δ -10.4 (d, J = 16.8 Hz), -10.54 (d, J= 18.6 Hz), -21.95 (t, J= 19.3 Hz); ¹⁹F NMR (D₂O, 376 MHz) δ -20.47 (m); MS (m/z): 803

EXAMPLE 14

Synthesis of m^{7l 2}'^"FG[S']ppp[5']m⁷G (Compound 20):

[0122] To a stirred solution of m^GDP 17 (0.25 g, 0.38 mmol) and Imidazolide m⁷GMP (m⁷-ImGMP) (0.24g, 0.57 mmol) in 10.0 mL dry DMF, Zinc chloride (0.10 g, 0.76 mmol) was added under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 6 h. After 6 h, the reaction mixture was added to a solution of EDTA disodium (0.57 g, 1.52 mmol) in 100.0 mL of water at 0⁰C. The resulting aqueous solution was adjusted to pH 5.5 with saturated NaHCOsand loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fraction O_CLs=- containing the product were pooled, evaporated and concentrated to 10.0 mL TEA salt of compound 20. The resulting 10.0 mL was passed through a Strata-X-AW column and washed with 10.0 mL water followed by 10.0 mL MeOH. Then, compound 20 was eluted with 15.0 mL OfNH₄OHZMeOHZH₂O (2Z25Z73) and the collected solution was evaporated and dried to give m^{7> 2 "F}Gpρpm⁷G as a fine white powder (compound 20) (Yield: 0.21 g, 64%).

[0123] Data for 20: ¹HNMR (D₂O, 400 MHz) δ 6.31 (d, J= 14.8 Hz, IH), 6.02 (d, J- 3.2 Hz, IH), 5.53 - 5.37 (m, IH), 4.75 - 4.62 (m, 2H), 4.52 - 4.38 (m, 5H)₅4.30 - 4.21 (m, 2H), 4.1 1 (s, 6H); ³¹P NMR (D₂0, 162 MHz) δ -10.35 (d, J= 11.8 Hz), -10.50 (d, J= 10.0 Hz), -21.80 (t, J= 19.1 Hz); ¹⁹FNMR (D₂0, 376 MHz) δ -20.51 (m); MS (mZz): 817 [M]⁺.

EXAMPLE 15 rt

Synthesis of m₂ ⁷'^2'0G[5'lppp[5']m^2'0G (Compound 23):

[0124] To a stirred solution of m₂ ⁷'^2'°GDP (N7Me2'O-MeGDP) 21 (0.22 g, 0.33 mmol) and Imidazolide m^2'°[GMP (Im2'O-MeGMP) 22 (0.14g, 0.33 mmol) in 10.0 mL dry DMF₅ Zinc chloride (0.09 g, 0.66 mmol) was added under nitrogen atmosphere and the reaction mixture was stirred at room temperaturefor 2 h. After 2 h, the reaction mixture was added to a solution of EDTA disodium (0.49 g, 1.32 mmol) in 100.0 mL of water at 0⁰C. The resulting aqueous solution was adjusted to pH 5.5 with saturated NaHCO₃ and loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and concentrated to 10.0 mL TEA salt of compound 23. The resulting 10.0 mL was passed through a Strata-X-AW column and washed with 10.0 mL water followed by 10.0 mL MeOH. Then, compound 23 was eluted with 15.0 mL OfNH₄OHMeOHyH₂O (2/25/73) and the collected solution was evaporated and dried to give mj'¹ °G[5']ppp[5']m^{2 0}G as a fine white powder (compound 23) (Yield: 0.18 g, 63%).

[0125] Data for 23: ¹H NMR (D₂0, 400 MHz) δ 8.00 (s, 2H), 5.90 (d, J= 2.0 Hz, IH), 5.83 (d, J= 5.2 Hz, IH), 4.59 (t, J= 4.4 Hz, IH), 4.53 - 4.41 (m, 2H), 4.33 - 4.22 (m, 6H), 4.16 (m, IH), 4.06 (s, 3H), 3.60 (s, 3H), 3.45 (s, 3H); ³¹P NMR (D₂O, 162 MHz) δ - 10.35 (t, J= 17.8 Hz), -21.83 (t, J= 18.0 Hz); MS (m/z): 831 [M]⁺-

EXAMPLE 16

rt

21 24

Synthesis of TO₂ ^{712 0}G[S⁵IpPp[S⁹Im₂ ^{712 0}G (Compound 25):

[0126] To a stirred solution of m₂ ^{7> 2'}°GDP (N7Me2 '-0-MeGDP) 21 (0.18 g, 0.27 mmol) and Imidazolide m₂ ^7>2'0GMP (Im N7Me-2^'-O-MeGMP) 24 (0.18g, 0.41 mmol) in 10.0 mL dry DMF, Zinc chloride (0.07 g, 0.54 mmol) was added under nitrogen atmosphere and the reaction mixture was stirred at room temperaturefor 6 h. After 6 h, the reaction mixture was added to a solution of EDTA disodium (0.40 g, 1.08 mmol) in 100.0 mL of water at O⁰C. The resulting aqueous solution was adjusted to pH 5.5 with saturated NaHCO₃ and loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and concentrated to 10.0 mL TEA salt of compound 25. The resulting 10.0 mL was passed through a Strata-X-AW column and washed with 10.0 mL water followed by 10.0 mL MeOH. Then, compound 25 was eluted with 15.0 mL of NH₄OHyMeOHZH₂O (2/25/73) and the collected solution was evaporated and dried to give m₂ ⁷'^2'°G[5']ppp[5']m₂ ^7l2'oG as a fine white powder (compound 25) (Yield: 0.13 g, 54%).

[0127] Data for 25: ¹H NMR (D₂O₅400 MHz) δ 6.10 (d, J= 2.8 Hz₅2H)₅4.59 (t, J = 5.2 Hz, 2H), 4.43 - 4.23 (m₅ 8H), 4.11 (s, 6H), 3.61 (s, 6H); ³¹P NMR (D₂0, 162 MHz) δ -10.32 (d, J= 18.] Hz), -21.72 (t, J= 20.7 Hz); MS (m/z): 845 [M-H]⁺.

EXAMPLE 17

rt

21

Synthesis of m₂ ^{7 ro}G[5']ppp[5']in⁷G (Compound 26):

[0128] To a stirred solution of m₂ ⁷'^2'°GDP (N7Me2⁵ -0-MeGDP) 21 (0.20 g, 0.3 mmol) and Imidazolide m⁷GDP QmN⁷MeGMP) (0.19 g, 0.45 mmol) in 10.0 mL dry DMF, Zinc chloride (0.08 g, 0.6 mmol) was added under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 6 h. After 6 h, the reaction mixture was added tb a solution of EDTA disodium (0.45 g, 1.2 mmol) in 100.0 mL of water at O⁰C. The resulting aqueous solution was adjusted to pH 5.5 with saturated NaHCOsand loaded on a DEAE Sephadex column. The desired product was eluted using a linear gradient of 0 - IM TEAB buffer, pH 7.5 and the fractions containing the product were pooled, evaporated and concentrated to 10.0 mL TEA salt of 26. The resulting 10.0 mL was passed through a Strata-X-AW column and washed with 10.0 mL water followed by 10.0 mL MeOH. Then, compound 26 was eluted with 15.0 mL OfNH₄OHZMeOHZH₂O (2Z25Z73) and the collected solution was evaporated and dried to give a fine white powder (compound 26) (Yield: 0.16 g, 62%)

[0129] Data for 26: ¹H NMR (D₂0, 400 MHz) δ 6.10 (d, J= 2.8 Hz, IH)₅ 6.01 (d, J = 3.6 Hz, IH), 4.63 (t, J= 5.6 Hz, IH), 4.58 (t, J= 5.6 Hz, IH)₅ 4.49 (t, J= 5.6 Hz₅ IH), 4.41 - 4.31 (m, 5H), 4.27 - 4.23 (m, 2H), 4.12 (s, 6H), 3.60 (s, 3H); ³¹P NMR (D₂O₅ 162 MHz) δ -10.36 (d, J= 19.0 Hz)₅ -21.77 (t, J= 19.3 Hz); MS (mZz): 829 [M]⁺.

EXAMPLE 18 T7 RNA Transcription:

[0130] T7 RNA polymerase transcription was performed by using mMESSAGE mMACHINE® T7 Kit (Ambion) in 20 μL final volume, and contains the following reagents at the final concentrations indicated: 1 μg linearized AmbLuc PoIyA DNA, IX reaction buffer,7.5mM of each ATP₅ UTP, and CTP₅ 1.5mM GTP₅ 6.5 raM of mCAP and 2' fluoro cap analogs, and 50 UZμl of T7 RNA polymerase. The transcription reactions were incubated at 37⁰C for 2 hours. In order to hydrolyze the remaining plasmid DNA₅ 1 μL of turbo DNAse was added to the reaction mixture, and further incubated at 37⁰C for 15 minutes. The transcribed capped and uncapped mRNAs were purified by using the MEGAclear™ Kit (Ambion).

[0131] AmbLuc PoIy(A) (Ambion), transcription produced comparable yields for modified and standard cap analogs (see Figures 5 and 6). The Bioanalyzer assay indicates that all the mRNAs are not degraded and retain great integrity (see Figure T).

EXAMPLE 19 Translation Assay:

[0132] Protein expression from mCAP, double methylated, triple methylated, and ARCA capped luciferase RNAs, at different time points after transfection with HeLa cells indicates that the transcripts containing triple methylated cap are more highly translated in transfected cells. Comparison of protein expression with mCAP and double methylated cap suggest that the double methylated cap transcript produces one fold higher protein, while ARCA produces 3 fold higher, and triple methylated cap produces 4 fold higher protein in in vivo with HeLa cells. See Figure 9.

[0133] All modified cap compounds tested are substrates for T7 polymerase, as determined by gel shift assays that clearly revealed that capped RNAs were formed, based on slower migration relative to uncapped RNAs (see Figures 8 and 10).

[0134] The examples above described particular cap analogs, however, there are additional cap analogs conceived which will also function in practicing the invention as illustrated below:

General Structure of CAP

EXAMPLE 20

[0135] The coupling reaction of m^'^GDP (N7Me-2'FGDP) with Imidazolide ²⁷OMP (lm2'FGMP), or Imidazolide m^7>2'FGMP (N7MeIm2TGMP) in the presence of ZnCI₂ as the catalyst affords the corresponding cap analogs A and B.

EXAMPLE 21

[0136] The coupling reaction of m^7>3WHjGDP (N7Me-3 'NH₂GDP) with Imidazolide ²⁷⁷GMP (lm2'FGMP), or Imidazolide m^GMP (N7MeIm2'FGMP) in the presence of ZnCl₂ as the catalyst affords the corresponding cap analogs E and F.

EXAMPLE 22

The coupling reaction of m⁷'^3VWj2dGDP (N7Me-3'NH₂2'dGDP) with the corresponding substituted Imidazolide GMP (ImGMP), Imidazolide m⁷GMP (m7-ImGMP), Imidazolide ^2F GMP (lm2'FGMP), or Imidazolide m⁷"^2"^ GMP (N7MeIm2 'FGMP)₅ respectively, in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs K, L₅ M, and N.

Scheme to Make C, D, G, H, I, J, O, P, Q, and R:

EXAMPLE 23

Scheme to Make m^7l3'CFjG[5 ]ppp[5']G and πT^'Gβ^'lpppβ ] m⁷G: [0138] The coupling reaction of m⁷-^ycFjGO? (N7Me-3 'CF₃GDP) with Imidazolide

GMP (ImGMP) or Imidazolide m⁷GMP (m⁷-ImGMP) in the presence of ZnCl₂ as the catalyst affords the corresponding cap analogs C and D.

EXAMPLE 24

[0139] T he coupling reaction of m⁷'^3WO'GDP (N7Me-3 'NO₂GDP) or m⁷-^3w^GDP (N7Me-3'NH₃GDP) with Imidazolide GMP (ImGMP) or Imidazolide m⁷GMP (m⁷- ImGMP) in the presence Of ZnCl₂ as the catalyst affords the corresponding cap analogs G, H, I, and J.

EXAMPLE 25

[0140] T he coupling reaction of m⁷'^3W<jDP (N7Me-3 'N₃GDP) with Imidazolide

GMP (ImGMP) or Imidazolide m⁷GMP (m⁷-ImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs O and P.

EXAMPLE 26

[0141] The coupling reaction of m^7>3Wj2^'dGDP (N7Me-3'N₃2'dGDP) with Imidazole GMP (ImGMP) or Imidazolide m⁷GMP (m7-ImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs Q and R.

EXAMPLE 27

The coupling reaction of m₂ ^{7>3 O}GDP (N7Me-3 OMe-GDP) with Imidazolide m^2'°GMP (Imm²'°GMP) or Imidazolide m₂ ^7a'oGMP (N7Me-2 'OMeImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs S and T.

EXAMPLE 28

The coupling reaction of m⁷'³'^c"°GDP (N7Me-3 'CHOGDP) with Imidazolide GMP (ImGMP) or Imidazolide m⁷GMP (m7-ImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs U and V. EXAMPLE 29

The coupling reaction of m₂ ⁷'^3'°GDP (N7Me-3 'OMeGDP) with Imidazolide ^ZFGMP (lm2'FGMP) or Imidazolide m⁷'^2'FGMP (N7MeIm2'FGMP) in the presence of ZnCl₂ as the catalyst affords the corresponding cap analogs W and X.

EXAMPLE 30

The coupling reaction of m⁷'^3'F2^'dGDP (N7Me-3'F-2'dGDP) or m⁷'^3's2^'dGDP (N7Me-3'S-2'dGDP) with Imidazolide GMP (ImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs Y and Z.

EXAMPLE 31

_m ^7,2Ttø^Ms_GMp (N7Me-2'TBDMS-GMP) with Imidazolide GMP (ImGMP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs Aa and Bb.

EXAMPLE 32

The coupling reaction of m^7>LNAGDP (N 7Me-LNA-GDP) with Imidazolide GDP (ImGDP) or Imidazolide m⁷GDP (m7-ImGDP) in the presence of ZnCl₂ as the catalyst affords the corresponding cap analogs Cc and Dd.

EXAMPLE 33

[0148] The coupling reaction of m⁷-^2'3' ^b°^Pr°^py'^idineGDP (N7Me- 2'3'isopropylideneGDP) with Imidazolide GDP (ImGDP) or Imidazolide m⁷GDP (m7- ImGDP) in the presence OfZnCl₂ as the catalyst affords the corresponding cap analogs Ee and Ff.

[01491 Although the present disclosure is described with respect to certain embodiments and examples, various modifications may be made without departing from the spirit and scope of the invention.

Claims

What is claimed: 1. A composition comprising

wherein:

A is selected from a halogen, OH, OCH₃, H, tert-butyldimethylsilyl and 2',3 '-O-isopropylidene;

B is selected from a halogen, OH₅ OCH₃, NH_2, N_3, NO₂, CF₃, CHO, S₅ ferf-butyldimethylsilyl, LNA, and 2',3 '-O-isopropylidene;

R₁ is CH₃ or void;

R₂ is selected from OH, OCH₃ and a halogen; n is 1, 2 or 3; and when B is OH or OCH_3, R₁ is void, and R₂ is OH₅ then A is neither OH nor OCH₃, and when A₅ B and R₂ are OH, R₁ is not CH₃.

2. The composition as recited in claim 1, wherein A is fluorine.

3. The composition as recited in claim I₅ wherein B is fluorine.

4. The composition as recited in claim 1 , wherein R₂ is fluorine.

5. The composition as recited in claim 1 attached to the 5' end of an RNA molecule.

6. The composition as recited in claim 2 attached to the 5' end of an RNA molecule.

7. The composition as recited in claim 3 attached to the 5' end of an RNA molecule.

8. The composition as recited in claim 4 attached to the 5' end of an RNA molecule.

9. The composition as recited in claim 1 , wherein:

A is selected from a halogen, OH₅ OCH₃, H, *er/-butyldimethylsilyl and 2'₅3'-O- isopropylidene; B is selected from a halogen, OH, OCH₃, NH₂, N₃, NO₂, CHO, S₅ tert- butyldimethylsilyl, LNA, and 2',3'-0-isopropylidene;

Ri is void;

R₂ is selected from OH, OCH₃ and a halogen; n is 1, 2 or 3; and when A is either OH or OCH₃, then R₂ is not OH.

10. The composition as recited in claim 9, wherein A is fluorine.

11. The composition as recited in claim 9, wherein B is fluorine.

12. The composition as recited in claim 9, wherein R₂ is fluorine.

13. The composition as recited in claim 9 attached to the 5' end of an RNA molecule.

14. The composition as recited in claim 10 attached to the 5' end of an RNA molecule.

15. The composition as recited in claim 11 attached to the 5' end of an RNA molecule.

16. The composition as recited in claim 12 attached to the 5' end of an RNA molecule.

17. The composition as recited in claim 1, wherein:

A is selected from a halogen, OH, OCH₃, H,-and 2',3'-O-isopropylidene;

B is selected from CF_3, OH, OCH₃, NH_2, N_3, NO₂, CHO, LNA, and 2',3'- O-isopropylidene;

Ri is CH₃;

R₂ is selected from OH, OCH₃ and a halogen; n is I₅2 or 3, and when A is OH, R₂ is not OH.

18. The composition as recited in claim 17, wherein A is fluorine.

19. The composition as recited in claim 17, wherein R₂ is fluorine.

20. The composition as recited in claim 17 attached to the 5' end of an RNA molecule.

21. The composition as recited in claim 18 attached to the 5' end of an RNA molecule.

22. The composition as recited in claim 19 attached to the 5' end of an RNA molecule.

23. The composition as recited in claim 1, comprising the structure wherein:

A is selected from OH and OCH₃;

B is selected from OH and OCH₃;

R₁ is CH₃;

R₂ is OCH₃; and n is 1, 2 or 3.

24. The composition as recited in claim 23, wherein A is OH and B is OCH₃.

25. The composition as recited in claim 23, wherein A is OCH₃ and B is OH

26. The composition as recited in claim 23 attached to the 5' end of an RNA molecule.

27. The composition as recited in claim 24 attached to the 5' end of an RNA molecule.

28. The composition as recited in claim 25 attached to the 5' end of an RNA molecule.

29. A kit for capping an RNA transcript comprising: a) an cap analog having the structure:

wherein:

A is selected from a halogen, OH, OCH3, H, tert-butyldimethylsilyl and 2',3'-O-isopropylidene;

B is selected from a halogen, OH, OCH₃, NH₂,N_3iNO₂,CF_3>CHO, S, /er/-butyldimethylsilyl, LNA, and 2',3'-O-isopropylidene; Ri is CH3 or void;

R₂ is selected from OH, OCH₃ and a halogen; n is 1, 2 or 3; and when B is OH or 0CH_3> R] is void, and R₂ is OH, then A is neither OH nor OCH₃, and when A, B and R₂ are OH, Ri is not CH3, and b). RNA polymerase.

30. A method of synthesizing a dinucleotide cap analog comprising: a) providing a first nucleoside comprising at least one of a 2' substituent and a 3' substituent on the ribose ring, b) phosphorylating the first nucleoside, forming a first nucleotide, c) methylating the first nucleotide, d) adding a phosphorylated second nucleotide optionally comprising a T ribose ring substituent, ,and e) linking said first nucleotide with said second nucleotide, forming a dinucleotide cap analog.

31. The method of claim 30 wherein said ribose ring comprises a substituent at the 2' position.

32. The method of claim 31 wherein the 2' substituent is selected from a halogen, OH, OCH₃, H, ter/-butyldimethylsilyl and 2',3'-O-isopropylidene.

33. The method of claim 32 wherein the halogen is fluorine.

34. The method of claim 30 wherein said ribose ring comprises a substituent at the 3' position.

35. The method of claim 34 wherein the 3' substituent is selected from a halogen, OH, OCH₃, NH₂, N₃, NO₂, CF₃, CHO, S, tert-butyldimethylsilyl, LNA, and 2',3'- O-isopropylidene.

36. The method of claim 35 wherein the halogen is fluorine.

37. The method of claim 30 wherein said step e) is followed by f) methylating said second nucleotide.

38. The method of claim 30 wherein said first nucleoside is guanosine.

39. The method of claim 38 wherein step c) comprises methylating the N7 position on the nucleotide.

40. The method of claim 30 wherein said second nucleotide is guanylic acid.

41. The method of claim 30 wherein the 2' substituent of said second nucleotide is a halogen, OH or CH₃.

42. The method of claim 41 wherein the halogen is fluorine.

43. The method of claim 30 further comprising f) methylating said second nucleotide.

44. The method of claim 43 wherein step f) comprises methylating position N7.

45. The method of claim 30 wherein said linking is catalyzed by ZnCl₂.

46. The kit of claim 29 further comprising nucleotides.

47. The kit of claim 29 further comprising ribonuclease inhibitor.

48. The kit of claim 29 further comprising enzyme buffer.

49. The kit of claim 29 further comprising nucleotide buffer.