ARTIFICAL ANTIBODY POLYPEPTIDES

• US 20020019517A1
• Filed: 06/12/1998
• Published: 02/14/2002
• Est. Priority Date: 06/12/1997
• Status: Active Grant

• Current Assignee: Novartis International Pharmaceutical Limited (Novartis Ag)
• Original Assignee: Research Corporation Technologies
• Inventors: KOIDE, SHOHEI
• Granted Patent: US 6,673,901 B2
• Time in Patent Office: Days
• US Class Current: 530/387.1
• CPC Class Codes: C07K 14/78 Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
• CPC Class Codes: C07K 16/00 Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies antibodies with enzymatic activity, e.g. abzymes C12N9/0002
• CPC Class Codes: C07K 16/18 against material from animals or humans
• CPC Class Codes: C07K 16/40 against enzymes
• CPC Class Codes: C07K 2317/565 Complementarity determining region [CDR]
• CPC Class Codes: C07K 2318/20 Antigen-binding scaffold molecules wherein the scaffold is not an immunoglobulin variable region or antibody mimetics
• CPC Class Codes: C12N 15/1037 Screening libraries presented on the surface of microorganisms, e.g. phage display, E. coli display
• CPC Class Codes: C12N 15/1044 Preparation or screening of libraries displayed on scaffold proteins
• CPC Class Codes: C40B 40/02 Libraries contained in or displayed by microorganisms, e.g. bacteria or animal cells; Libraries contained in or displayed by vectors, e.g. plasmids; Libraries containing only microorganisms or vectors
• CPC Class Codes: G01N 2333/78 Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG]
• CPC Class Codes: G01N 33/68 involving proteins, peptides or amino acids involving lipoproteins G01N33/92
• CPC Class Codes: G01N 33/6845 Methods of identifying protein-protein interactions in protein mixtures
• CPC Class Codes: G01N 33/78 Thyroid gland hormones , e.g. T3, T4, TBH, TBG or their receptors

Abstract

A fibronectin type III (Fn3) polypeptide monobody, a nucleic acid molecule encoding said monobody, and a variegated nucleic acid library encoding said monobody, are provided by the invention. Also provided are methods of preparing a Fn3 polypeptide monobody, and kits to perform said methods. Further provided is a method of identifying the amino acid sequence of a polypeptide molecule capable of binding to a specific binding partner (SBP) so as to form a polypeptide:SSP complex, and a method of identifying the amino acid sequence of a polypeptide molecule capable of catalyzing a chemical reaction with a catalyzed rate constant, k_cat, and an uncatalyzed rate constant, k_uncat, such that the ratio of k_cat/k_uncat is greater than 10.

Claims

1. A fibronectin type III (Fn3) polypeptide monobody comprising a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences,

wherein one or more of the monobody loop region sequences vary by deletion, insertion or replacement of at least two amino acids from the corresponding loop region sequences in wild-type Fn3, and

wherein the β

-strand domains of the monobody have at least a 50% total amino acid sequence homology to the corresponding amino acid sequence of wild-type Fn3'"'"'s β

-strand domain sequences.

2. The monobody of claim 1, wherein at least one loop region is capable of binding to a specific binding partner (SBP) to form a polypeptide:

SBP complex having a dissociation constant of less than 104 moles/liter.

3. The monobody of claim 1, wherein at least one loop region is capable of catalyzing a chemical reaction with a catalyzed rate constant (k_cat) and an uncatalyzed rate constant (k_uncat) such that the ratio of k_cat/k_uncat is greater than 10.

4. The monobody of claim 1, wherein one or more of the loop regions comprise amino acid residues:

i) from 15 to 16 inclusive in an AB loop;

ii) from 22 to 30 inclusive in a BC loop;

iii) from 39 to 45 inclusive in a CD loop;

iv) from 51 to 55 inclusive in a DE loop;

v) from 60 to 66 inclusive in an EF loop; and

vi) from 76 to 87 inclusive in an FG loop.

5. The monobody of claim 1, wherein the monobody loop region sequences vary from the wild-type Fn3 loop region sequences by the deletion or replacement of at least 2 amino acids.

6. The monobody of claim 1, wherein the monobody loop region sequences vary from the wild-type Fn3 loop region sequences by the insertion of from 3 to 25 amino acids.

7. An isolated nucleic acid molecule encoding the polypeptide monobody of claim 1.

8. An expression vector comprising an expression cassette operably linked to the nucleic acid molecule of claim 7.

9. The expression vector of claim 8, wherein the expression vector is an M13 phage-based plasmid.

10. A host cell comprising the vector of claim 8.

11. A method of preparing a fibronectin type ml (Fn3) polypeptide monobody comprising the steps of:

a) providing a DNA sequence encoding a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences wherein at least one loop region contains a unique restriction enzyme site;

b) cleaving the DNA sequence at the unique restriction site;

c) inserting into the restriction site a DNA segment known to encode a peptide capable of binding to a specific binding partner (SBP) or a transition state analog compound (TSAC) so as to yield a DNA molecule comprising the insertion and the DNA sequence of (a); and

d) expressing the DNA molecule so as to yield polypeptide monobody.

14. A kit for performing the method of any one of claims 11-13, comprising a replicatable DNA encoding a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences.

16. The variegated nucleic acid library of claim 15, wherein one or more of the loop regions encodes:

i) an AB amino acid loop from residue 15 to 16 inclusive;

ii) a BC amino acid loop from residue 22 to 30 inclusive;

iii) a CD amino acid loop from residue 39 to 45 inclusive;

iv) a DE amino acid loop from residue 51 to 55 inclusive;

v) an EF amino acid loop from residue 60 to 66 inclusive; and

vi) an FG amino acid loop from residue 76 to 87 inclusive.

17. The variegated nucleic acid library of claim 15, wherein the loop region sequences vary from the wild-type Fn3 loop region sequences by the deletion or replacement of at least 2 amino acids.

18. The variegated nucleic acid library of claim 15, wherein the monobody loop region sequences vary from the wild-type Fn3 loop region sequences by the insertion of from 3 to 25 amino acids.

19. The variegated nucleic acid library of claim 15, wherein a variegated nucleic acid sequence comprising from 6 to 75 nucleic acid bases is inserted in any one of the loop regions of said species.

20. The variegated nucleic acid library of claim 15, wherein the variegated sequence is constructed so as to avoid one or more codons selected from the group consisting of those codons encoding cysteine or the stop codon.

21. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the BC loop.

22. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the DE loop.

23. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the FG loop.

24. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the AB loop.

25. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the CD loop.

26. The variegated nucleic acid library of claim 15, wherein the variegated nucleic acid sequence is located in the EF loop.

27. A peptide display library derived from the variegated nucleic acid library of claim 15.

28. A peptide display library of claim 27, wherein the peptide is displayed on the surface of a bacteriophage or virus.

29. A peptide display library of claim 28, wherein the bacteriophage is M13 or fd.

30. A method of identifying the amino acid sequence of a polypeptide molecule capable of binding to a specific binding partner (SBP) so as to form a polypeptide:

SSP complex wherein the dissociation constant of the said polypeptide;

SBP complex is less than 10<sup>−

6</sup> moles/liter, comprising the steps of;

a) providing a peptide display library according to claim 28;

b) contacting the peptide display library of (a) with an immobilized or separable SBP;

c) separating the peptide;

SBP complexes from the free peptides,

d) causing the replication of the separated peptides of (c) so as to result in a new peptide display library distinguished from that in (a) by having a lowered diversity and by being enriched in displayed peptides capable of binding the SBP;

e) optionally repeating steps (b), (c), and (d) with the new library of (d); and

f) determining the nucleic acid sequence of the region encoding the displayed peptide of a species from (d) and deducing the peptide sequence capable of binding to the SBP.

32. A method of identifying the amino acid sequence of a polypeptide molecule capable of catalyzing a chemical reaction with a catalyzed rate constant, k_cat, and an uncatalyzed rate constant, k_uncat, such that the ratio of k_cat/k_uncat is greater than 10, comprising the steps of:

a) providing a peptide display library according to claim 28;

b) contacting the peptide display library of (a) with an immobilized or separable transition state analog compound (TSAC) representing the approximate molecular transition state of the chemical reaction;

c) separating the peptide;

TSAC complexes from the free peptides;

d) causing the replication of the separated peptides of (c) so as to result in a new peptide display library distinguished from that in (a) by having a lowered diversity and by being enriched in displayed peptides capable of binding the TSAC;

e) optionally repeating steps (b), (c), and (d) with the new library of (d); and

f) determining the nucleic acid sequence of the region encoding the displayed peptide of a species from (d) and hence deducing the peptide sequence.

34. An isolated polypeptide identified by the method of claim 30

35. An isolated polypeptide identified by the method of claim 32.

36. A kit for identifying the amino acid sequence of a polypeptide molecule capable of binding to a specific binding partner (SBP) so as to form a polypeptide:

SSP complex wherein the dissociation constant of the said polypeptide;

SBP complex is less than 10<sup>−

6</sup> moles/liter, comprising the peptide display library of claim 28.

37. A kit for identifying the amino acid sequence of a polypeptide molecule capable of catalyzing a chemical reaction with a catalyzed rate constant, k_cat, and an uncatalyzed rate constant, k_uncat, such that the ratio of k_cat/k_uncat is greater than 10, comprising the peptide display library of claim 28.

39. A polypeptide derived by using the kit of claim 37.

12. A method of preparing a fibronectin type III (Fn3) polypeptide monobody comprising the steps of:

(a) providing a replicatable DNA sequence encoding a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences, wherein the nucleotide sequence of at least one loop region is known;

(b) preparing polymerase chain reaction (PCR) primers sufficiently complementary to the known loop sequence so as to be hybridizable under PCR conditions, wherein at least one of the primers contains a modified nucleic acid sequence to be inserted into the DNA;

(c) performing polymerase chain reaction using the DNA sequence of (a) and the primers of (b);

(d) annealing and extending the reaction products of (c) so as to yield a DNA product; and

(e) expressing the polypeptide monobody encoded by the DNA product of (d).

13. A method of preparing a fibronectin type III (Fn3) polypeptide monobody comprising the steps of:

a) providing a replicatable DNA sequence encoding a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences, wherein the nucleotide sequence of at least one loop region is known;

b) performing site-directed mutagenesis of at least one loop region so as to create a DNA sequence comprising an insertion mutation; and

c) expressing the polypeptide monobody encoded by the DNA sequence comprising the insertion mutation.

15. A variegated nucleic acid library encoding Fn3 polypeptide monobodies comprising a plurality of nucleic acid species each comprising a plurality of loop regions, wherein the species encode a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences,

wherein one or more of the loop region sequences vary by deletion, insertion or replacement of at least two amino acids from corresponding loop region sequences in wild-type Fn3, and

wherein the β

-strand domain sequences of the monobody have at least a 50% total amino acid sequence homology to the corresponding amino acid sequences of β

-strand domain sequences of the wild-type Fn3.

31. A method of preparing a variegated nucleic acid library encoding Fn3 polypeptide monobodies having a plurality of nucleic acid species each comprising a plurality of loop regions, wherein the species encode a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences, wherein one or more of the loop region sequences vary by deletion, insertion or replacement of at least two amino acids from corresponding loop region sequences in wild-type Fn3, and wherein the β

-strand domain sequences of the monobody have at least a 50% total amino acid sequence homology to the corresponding amino acid sequences of β

-strand domain sequences of the wild-type Fn3, comprising the steps of

a) preparing an Fn3 polypeptide monobody having a predetermined sequence;

b) contacting the polypeptide with a specific binding partner (SBP) so as to form a polypeptide;

SSP complex wherein the dissociation constant of the said polypeptide;

SBP complex is less than 10<sup>−

6</sup> moles/liter;

c) determining the binding structure of the polypeptide;

SBP complex by nuclear magnetic resonance spectroscopy or X-ray crystallography; and

d) preparing the variegated nucleic acid library, wherein the variegation is performed at positions in the nucleic acid sequence which, from the information provided in (c), result in one or more polypeptides with improved binding to the SBP.

33. A method of preparing a variegated nucleic acid library encoding Fn3 polypeptide monobodies having a plurality of nucleic acid species each comprising a plurality of loop regions, wherein the species encode a plurality of Fn3 β

-strand domain sequences that are linked to a plurality of loop region sequences, wherein one or more of the loop region sequences vary by deletion, insertion or replacement of at least two amino acids from corresponding loop region sequences in wild-type Fn3, and wherein the β

-strand domain sequences of the monobody have at least a 50% total amino acid sequence homology to the corresponding amino acid sequences of β

-strand domain sequences of the wild-type Fn3, comprising the steps of

a) preparing an Fn3 polypeptide monobody having a predetermined sequence, wherein the polypeptide is capable of catalyzing a chemical reaction with a catalyzed rate constant, k_cat, and an uncatalyzed rate constant, k_uncat, such that the ratio of k_cat/k_uncat is greater than 10;

b) contacting the polypeptide with an immobilized or separable transition state analog compound (TSAC) representing the approximate molecular transition state of the chemical reaction;

c) determining the binding structure of the polypeptide;

TSAC complex by nuclear magnetic resonance spectroscopy or X-ray crystallography; and

d) preparing the variegated nucleic acid library, wherein the variegation is performed at positions in the nucleic acid sequence which, from the information provided in (c), result in one or more polypeptides with improved binding to or stabilization of the TSAC.

38. A polypepetide derived by using the kit of claim 36.