IP Library Granted Patent US 9,783,843
Granted Patent B2
US 9,783,843 · App. 14/155,031 · Granted Oct 10, 2017

Encoded self-assembling chemical libraries (esachel)

Inventors: Dario Neri (Zurich, CH); Samu Melkko (Zurich, CH)
Assignee: Eidgenoessische Technische Hochschule Zurich
C12Q1/6837C07H21/00C12N15/1068C12Q1/6813C40B30/04C40B40/06G01N33/58C07H21/02C07H21/04
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Quick Facts
Patent No.
US 9,783,843
App. No.
14/155,031
Granted
Oct 10, 2017
Kind
B2
Abstract

The invention provides a chemical compound comprising a chemical moiety (p) capable of performing a binding interaction with a target molecule, and an oligonucleotide (b) or functional analogue thereof. The oligonucleotide (b) or functional analogue comprises at least one self-assembly sequence (b1) capable of performing a combination reaction with at least one self-assembly sequence (b1′) of a complementary oligonucleotide or functional analogue bound to another chemical compound comprising a chemical moiety (q). In some embodiments, the chemical compound comprises a coding sequence (b1) coding for the identification of the chemical moiety (p) and further comprises at least one self-assembly moiety (m) capable of performing a combination reaction with at least one self-assembly moiety (m′) of a similar chemical compound comprising a chemical moiety (q). The invention also provides corresponding libraries of chemical compounds as well as methods of biopanning of for target molecules and of identifying such targets.

Claims (23)

1. A chemical library comprising stable combination reaction products between a first number of chemical compounds of a sub-library A with a sublibrary B of chemical compounds, wherein the compounds of the sub-library A comprise:

(i) a chemical moiety (p) capable of performing a binding interaction with a single target molecule, coupled to

(ii) an oligonucleotide (b) or functional analogue thereof, which comprises a variable, unique distinctive sequence tag (b2) coding for the identification of the chemical moiety (p) of its compound and a common self-assembly sequence (b1) capable of performing a combination reaction and of building a stable combination reaction product with a common self-assembly sequence (b1′) of a plurality of chemical compounds of the sub-library B, wherein the sub-library B comprises a second number of chemical compounds each comprising:

(i) a chemical moiety (q) capable of performing a binding interaction with a single target molecule, coupled to

(ii) an oligonucleotide (b′) or functional analogue thereof, which comprises a variable, unique distinctive sequence tag (b2′) coding for the identification of the chemical moiety (q) of its compound, and the common self-assembly sequence (b1′),

wherein the chemical moieties (p,q) are small organic molecules;

wherein the stable combination reaction product comprises an oligomer and chemical moieties (p) and (q) are at the same terminus of the oligomer; and

wherein both chemical moieties (p,q) of the stable combination reaction product of one chemical compound of sub-library A and of one chemical compound of sub-library B bind to the same target molecule;

wherein in sub-library A or in sub-library B the oligonucleotides (b) or (b′), or functional analogues thereof, are coupled to chemical moieties (p,q) via a primary amino group at a 3′ or 5′ extremity.

2. The chemical library of claim 1 , wherein the chemical compounds of sub-library A and sub-library B are capable of forming stable combination reaction products in the absence of said target molecule(s).

3. The chemical library of claim 1 , wherein sub-library A and sub-library B each comprise at least four chemical compounds.

4. The chemical library of claim 1 , wherein the chemical compounds of each sub-library comprise a different chemical moiety (p,q) than other members of the respective sub-library.

5. The chemical library of claim 1 , wherein the chemical moieties (p) of sub-library A are coupled to a 3′ extremity of the oligonucleotide (b1), and wherein the chemical moieties (q) of sub-library B are coupled to a 5′ extremity of the oligonucleotide (b1′).

6. The chemical library of claim 1 , wherein said stable combination reaction products are derived by forming oligomers selected from the group comprising dimers, trimers, and tetramers, by hetero-oligomerization of the self-assembly sequences (b1,b1′) of the oligonucleotides (b,b′), thereby forming heteroduplexes, heterotriplexes or heteroquadruplexes.

7. The chemical library of claim 1 , wherein in sub-library A the self-assembly sequence (b1) is interrupted by a d-spacer, the d-spacer preventing any undesired pairing to the bases of distinctive sequence tag (b2′) which encodes sub-library B, and wherein the oligonucleotide (b) of sub-library A has its distinctive sequence tag (b2) towards the 5′ extremity.

8. The chemical library of claim 1 , wherein each chemical compound of sub-library A further comprises at least one chemical group that is capable of forming a covalent bond with at least one chemical group of a chemical compound of sub-library B with which had been formed a stable combination reaction product.

9. The chemical library of claim 1 , wherein in sub-library A, each oligonucleotide (b) or functional analogue thereof is directly and covalently linked to a chemical moiety (p) and wherein in sub-library B, each oligonucleotide (b′) of or functional analogue thereof is directly and covalently linked to a chemical moiety (q).

10. The chemical library of claim 1 , wherein in the chemical compounds of sub-library A and sub-library B, the respective oligonucleotides (b,b′) or functional analogues thereof further each comprise a linking portion which is situated between the respective self-assembly sequences (b1,b1′) and the respective chemical moieties (p,q).

11. The chemical library of claim 1 , wherein the sequences of the distinctive sequence tags (b2,b2′) of each oligonucleotide (b,b′) or the functional analogues thereof are situated between their respective chemical moieties (p,q) and their respective self-assembly sequences (b1,b1′).

12. The chemical library of claim 1 , wherein in the stable combination reaction products between members of sub-library A and sub-library B, the respective members in each stable combination reaction product are covalently linked to each other.

13. The chemical library of claim 1 , wherein the chemical moiety (p) and the chemical moiety (q) are not covalently linked.

14. The chemical library of claim 1 , wherein the target molecule is a protein.

15. The chemical library of claim 1 , wherein the chemical moieties (p,q) of the stable combination reaction product are different.

Continuity (5)
Continuation 12613475 · Nov 5, 2009
Continuation 12555707 · Sep 8, 2009
Continuation In Part 10507140 · Sep 19, 2005
Continuation 10382107 · Mar 5, 2003
Related Publication 20140128290A1 · May 8, 2014