Method For The Site-Specific Synthesis Of Biopolymers On Solid Supports
The present invention relates to methods for the site-specific synthesis of biopolymers such as nucleic acids or peptides and their respective derivatives on solid supports, wherein the local discrimination of the synthesis is performed by using masks that guide aqueous activating reagents for cleaving off protecting groups to predetermined regions on the support.
1 . Method for the site-specific synthesis of biopolymers in predetermined regions of a solid support by the successive coupling of monomeric and/or oligomeric building blocks, the biopolymers having a defined sequence wherein prior to each coupling step reactive groups that are available in at least one predetermined region of the support for the coupling of a monomeric and/or oligomeric building block are activated in that temporary protecting groups are removed from said reactive groups by adding an activating reagent in aqueous solution.
2 . Method according to claim 1 ,
wherein the temporary protecting groups are removed from such predetermined regions of the support that are predetermined by a mask that is arranged on the support.
3 . Method according to any of the preceding claims,
wherein the support has reactive groups for the coupling of monomeric and/or oligomeric building blocks.
4 . Method for the site-specific synthesis of biopolymers in predetermined regions of a solid support, the biopolymers having a defined sequence, comprising the following steps:
a) arranging a mask on the support, wherein reactive groups that are available on the support for the coupling of monomeric and/or oligomeric building blocks of the biopolymer to be synthesized are provided with protecting groups;
b) activating of reactive groups by removing of temporary protecting groups in the regions that are predetermined by the mask by adding an activating reagent in aqueous solution;
c) coupling of a monomeric and/or oligomeric building block to reactive groups that have been activated in step b); and
d) repeating the steps a) to c) until the desired biopolymers are synthesized in predetermined regions of the support.
5 . Method according to any of the preceding claims,
wherein the mask is separated from the support prior to a coupling step.
6 . Method according to any one of the preceding claims,
wherein the biopolymers are selected from nucleic acids, peptides, and peptide nucleic acids.
7 . Method according to any of the preceding claims,
wherein the temporary protecting groups are selected from dimethyloxytrityl, tert.-butyloxycarbonyl and/or fluorenyl-9-methoxycarbonyl.
8 . Method according to any of the preceding claims,
wherein the activating reagent is a deprotection reagent.
9 . Method according to claim 8 ,
wherein the deprotection reagent is selected from oxalic acid, methanesulfonic acid, trifluoroacetic acid, hydrochloric acid and/or sodium hydroxide.
10 . Method according to any of the preceding claims,
wherein the support is selected from silicon, silica, glass and/or ceramics.
11 . Method according to any of claims 2 to 10 ,
wherein the mask that is arranged on the support adheres to the support.
12 . Method according to any of claims 2 to 11 ,
wherein the mask comprises elastomers at least on the side that contacts the support.
13 . Method according to claim 12 ,
wherein the elastomer is polydimethylsiloxane.
14 . Method according to any of the preceding claims,
wherein the support has a rough surface.
15 . Method according to any of the preceding claims,
wherein the predetermined regions are separated from one another by regions that are inert to the synthesis of biopolymers.
16 . Method according to any of the preceding claims,
wherein the support has markings for arranging a mask on the support.
17 . Method according to any of the preceding claims,
wherein the support comprises 50 to 65,000 predetermined regions.
18 . Method according to any of the preceding claims,
wherein biopolymers that are synthesized in different predetermined regions differ with respect to their sequence.
19 . Method according to any of the preceding claims,
wherein the surface of the support is 100 μm 2 to 1 cm 2 and preferably 3 mm 2 to 25 mm 2 .
20 . Method according to any of the preceding claims,
wherein the sequences of the biopolymers are selected according to their suitability as molecular probes in microarray experiments.
21 . Use of a method according to any of claims 1 to 20 for manufacturing a microarray having biopolymer probes immobilized in predetermined regions.
22 . Use of a method according to any of claims 1 to 20 for manufacturing a microarray having biopolymer probes immobilized in predetermined regions, wherein the predetermined regions are separated from one another by inert regions.
23 . Microarray having biopolymer probes immobilized in predetermined regions, in which the percentage P of biopolymers that have the desired number M of monomers is characterized by the formula P=S M ,
wherein S is the average yield of a coupling step of a monomeric and/or oligomeric building block,
and wherein the density of predetermined regions is at least 1,500 predetermined regions per cm 2 and the average yield S is at least 95%, preferably at least 96%, particularly preferably at least 97%, and most preferably at least 98%.
24 . Microarray according to claim 22 , manufactured by a method according to any of claims 1 to 20 .
25 . Use of deprotection reagents in aqueous solution in the synthesis of biopolymers for cleaving off temporary protecting groups.