Oligonucleotides and analogs labeled with energy transfer dyes

Abstract

Novel linkers for linking a donor dye to an acceptor dye in an energy transfer fluorescent dye are provided. These linkers faciliate the efficient transfer of energy between a donor and acceptor dye in an energy transfer dye. One of these linkers for linking a donor dye to an acceptor dye in an energy transfer fluorescent dye has the general structure R 21 Z 1 C(O)R 22 R 28 where R 21 is a C 1-5 alkyl attached to the donor dye, C(O) is a carbonyl group, Z 1 is either NH, sulfur or oxygen, R 22 is a substituent which includes an alkene, diene, alkyne, a five and six membered ring having at least one unsaturated bond or a fused ring structure which is attached to the carbonyl carbon, and R 28 includes a functional group which attaches the linker to the acceptor dye.

1 . A fluorescently-labeled reagent comprising an oligonucleotide or an oligonucleotide analog and an energy transfer dye, wherein energy transfer dye is covalently linked to the oligonucleotide or oligonucleotide analog, and comprises:
 a fluorescein donor dye capable of absorbing light at a first wavelength and emitting excitation energy in response thereto;   a 4,7-dichlororhodamine acceptor dye capable of absorbing the excitation energy emitted by the donor dye and fluorescing at a second wavelength in response thereto; and   a non-nucleosidic linker linking the 5- or 6-position of the fluorescein donor dye to the 5- or 6-position of the 4,7-dichlororhodamine acceptor dye.   
     
     
         2 . The fluorescently-labeled reagent of  claim 1  in which the linker has a backbone that is less than 9 atoms in length. 
     
     
         3 . The fluorescently-labeled reagent of  claim 1  in which the linker comprises a functional group selected from an alkene, a diene, an alkyne, a five membered ring having at least one unsaturated bond, a six membered ring having at least one unsaturated bond and a fused ring structure. 
     
     
         4 . The fluorescently-labeled reagent of  claim 1  in which the energy transfer dye is covalently linked to the 5′-terminus of the oligonucleotide or oligonucleotide analog. 
     
     
         5 . The fluorescently-labeled reagent of  claim 1  in which the energy transfer dye is covalently linked to the 3′-terminus of the oligonucleotide or oligonucleotide analog. 
     
     
         6 . The fluorescently-labeled reagent of  claim 5  in which the energy transfer dye is covalently linked to a base moiety of the oligonucleotide or oligonucleotide analog. 
     
     
         7 . The fluorescently labeled reagent of  claim 6  in which energy transfer dye is covalently linked to the base moiety via the 4′-position of the fluorescein donor dye or the 4′-position of the 4,7-dichlororhodamine acceptor dye. 
     
     
         8 . The fluorescently labeled reagent of  claim 7  in which energy transfer dye is covalently linked to the base moiety by way of an acetylenic amido or alkenic amido linkage. 
     
     
         9 . The fluorescently labeled reagent of  claim 8  in which the acetylenic amido or alkenic amido linkage is selected from —C≡C—CH 2 —NH—C(O)—, 3-amino-1-propyn-1-yl, —C≡C—CH 2 —NH—C(O)—(CH 2 ) 5 —C(O)—, —C═CH—C(O)—NH—(CH 2 ) 5 —NH—C(O)— and —C≡C—CH 2 —O—CH 2 —CH 2 —NR—, where R is hydrogen, a protecting group or alkyl 
     
     
         10 . The fluorescently-labeled reagent of  claim 1  in which the 4,7-dichlororhodamine acceptor dye comprises structure (I): 
       
         
           
           
               
               
           
         
         wherein:
 R 1 , R 2 , R 3  and R 4  are each, independently of one another, selected from hydrogen and alkyl, or alternatively R 1  and R 5 , R 2  and R 6 , R 3  and R 8  and/or R 4  and R 9  are taken together with the atoms to which they are bonded to form a 5, 6 or 7-membered ring; 
 R 5 , R 6 , R 7 , R 8 , R 9  and R 10  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile, alkoxy, phenyl and substituted phenyl, or alternatively, R 6  and R 7  and/or R 9  and R 10  are taken together with the atoms to which they are bonded to form a benzo group; 
 X 1 , X 3  and X 4  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile and alkoxy; and 
 X 3  or X 4  comprises the non-nucleosidic linker linking the fluorescein donor dye. 
 
       
     
     
         11 . The fluorescently-labeled reagent of  claim 1  in which the fluorescein donor dye comprises structure (II): 
       
         
           
           
               
               
           
         
         wherein:
 R 11 , R 12 , R 13 , R 14 , R 15  and R 16  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile, alkoxy, phenyl and substituted phenyl, or alternatively, R 12  and R 13  and/or R 15  and R 16  are taken together with the atoms to which they are bonded to form a benzo group; 
 X 11 , X 12 , X 13 , X 14  and X 15  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile and alkoxy; and 
 X 13  or X 14  comprises the non-nucleosidic linker linking the 4,7-dichlororhodamine acceptor dye. 
 
       
     
     
         12 . The fluorescently-labeled reagent of  claim 1  in which energy transfer dye comprises structure (III): 
       
         
           
           
               
               
           
         
         wherein:
 R 1 , R 2 , R 3  and R 4  are each, independently of one another, selected from hydrogen, methyl and ethyl, or alternatively R 1  and R 5 , R 2  and R 6 , R 3  and R 8  and/or R 4  and R 9  are taken together with the atoms to which they are bonded to form a 5, 6 or 7-membered ring; 
 R 5 , R 6 , R 7 , R 8 , R 9  and R 10  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile, alkoxy, phenyl and substituted phenyl, or alternatively, R 6  and R 7  and/or R 9  and R 10  are taken together with the atoms to which they are bonded to form a benzo group; 
 X 1  and X 3  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile and alkoxy; 
 L is the non-nucleosidic linker; 
 R 11 , R 12 , R 13 , R 14 , R 15  and R 16  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile, alkoxy, phenyl and substituted phenyl, or alternatively, R 12  and R 13  and/or R 15  and R 16  are taken together with the atoms to which they are bonded to form a benzo group; and 
 X 11 , X 12 , X 13  and X 15  are each, independently of one another, selected from hydrogen, fluorine, chlorine, bromine, iodine, carboxyl, alkyl, alkene, alkyne, sulfonate, sulfone, amino, ammonium, amido, nitrile and alkoxy, 
 with the proviso that one of R 8  or R 14  comprises a linkage that covalently links the energy transfer dye to the oligonucleotide or oligonucleotide analog. 
 
       
     
     
         13 . The fluorescently labeled reagent of  claim 12  in which X 1  is carboxylate. 
     
     
         14 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10  and X 3  are each hydrogen. 
     
     
         15 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 3 , R 5 , R 7 , R 8 , R 10  and X 3  are each hydrogen; R 2  and R 4  are each ethyl; and R 6  and R 9  are each methyl. 
     
     
         16 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 2 , R 3  and R 4  are each methyl; and R 5 , R 6 , R 7 , R 8 , R 9 , R 10  and X 3  are each hydrogen. 
     
     
         17 . The fluorescently labeled reagent of  claim 13  in which R 1  and R 5 , R 2  and R 6 , R 3  and R 8  and R 4  and R 9  are taken together with the atoms to which they are bonded to form six-membered rings; and R 7 , R 10  and X 3  are each hydrogen. 
     
     
         18 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , R 10  and X 3  are each hydrogen; R 2  is ethyl; and R 6  is methyl. 
     
     
         19 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 5 , R 7 , R 8 , R 9 , R 10  and X 3  are each hydrogen; R 3 , R 4  and R 6  are each methyl; and R 2  is ethyl. 
     
     
         20 . The fluorescently labeled reagent of  claim 13  in which R 5 , R 6 , R 7 , R 10  and X 3  are each hydrogen; R 1  and R 2  are each methyl; and R 3  and R 8  and R 4  and R 9  are taken together with the atoms to which they are bonded to form six-membered rings. 
     
     
         21 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 2 , R 5 , R 6 , R 7 , R 10  and X 3  are each hydrogen; and R 3  and R 8  and R 4  and R 9  are taken together with the atoms to which they are bonded to form six-membered rings. 
     
     
         22 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 5 , R 6 , R 7 , R 10  and X 3  are each hydrogen; R 2  is ethyl; and R 3  and R 8  and R 4  and R 9  are taken together with the atoms to which they are bonded to form six-membered rings. 
     
     
         23 . The fluorescently labeled reagent of  claim 13  in which R 1 , R 2 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10  and X 3  are each hydrogen; and R 3  and R 4  are each methyl.