# US 10,766,924 B2 · Affinity support and method for isolating immunoglobulin

> Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt

- Number: US 10,766,924 B2
- Document ID: US10766924B2
- Status: Granted
- Kind: B2
- Application number: 15/745,855
- Filed: 2016-07-27
- Published: 2018-08-09
- Granted: 2020-09-08
- Earliest claimed: 2015-07-28
- Assignees: Jsr Corporation; Jsr Life Sciences Corporation
- Applicants: Jsr Corporation; Jsr Life Sciences Corporation
- Inventors: Takashi Ichii; Satoshi Nakamura; Jun-ichi Yasuoka; Kaori Itaya; Tomonori Shiotani
- Web page: https://patentgrep.com/patent/US10766924B2

## CPC

- C07K 1/22: Affinity chromatography or related techniques based upon selective absorption processes
- B01J 20/289: bonded via a spacer
- B01J 20/3204: {Inorganic carriers, supports or substrates}
- B01J 20/321: {consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds}
- B01J 20/3219: {involving a particular spacer or linking group, e.g. for attaching an active group}
- B01J 20/3248: {the functional group or the linking, spacer or anchoring group as a whole comprising at least one type of heteroatom selected from a nitrogen, oxygen or sulfur, these atoms not being part of the carrier as such}
- B01J 20/3255: {comprising a cyclic structure containing at least one of the heteroatoms nitrogen, oxygen or sulfur, e.g. heterocyclic or heteroaromatic structures}
- G01N 30/88: Integrated analysis systems specially adapted therefor, not covered by a single one of the groups G01N30/04 - G01N30/86
- G01N 2030/8831: {involving peptides or proteins}
- C07K: PEPTIDES (peptides in foodstuffs A23; obtaining protein compositions for foodstuffs, working-up proteins for foodstuffs A23J; preparations for medicinal purposes A61K; peptides containing beta-lactam rings C07D; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, C07D; ergot alkaloids of the cyclic peptide type C07D519/02; macromolecular compounds having statistically distributed amino acid units in their molecules, i.e. when the preparation does not provide for a specific; but for a random sequence of the amino acid units, homopolyamides and block copolyamides derived from amino acids C08G69/00; macromolecular products derived from proteins C08H1/00; preparation of glue or gelatine C09H; single cell proteins, enzymes C12N; genetic engineering processes for obtaining peptides C12N15/00; compositions for measuring or testing processes involving enzymes C12Q; investigation or analysis of biological material G01N33/00)
- B01J: CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q)

## Abstract

To provide an affinity support in which a binding property of a ligand to a target substance is improved. The affinity support contains a solid phase support and a protein ligand, wherein the protein ligand is represented by formula (1): R—R1 (1) wherein R represents a linker binding to the solid phase support, which contains a polyproline, and R1 represents a protein showing an affinity to immunoglobulin, and the R is bound to a C terminal or an N terminal of an amino acid sequence in R1.

## Claims

### Claim 1

An affinity support, comprising:
a solid phase support and
a protein ligand,
wherein the protein ligand has the following formula(1):
R—R1 (1),
wherein
R is a linker binding to the solid phase support, which comprises a polyproline comprising from 12 to 24 proline residues, and
R1 is a protein having an affinity to an immunoglobulin, and
R is bound to a C terminal or an N terminal of an amino acid sequence of the protein R1.

### Claim 2 (depends on 1)

The affinity support according to claim 1, wherein the linker has a length of from 3.6 nm to 7.3 nm.

### Claim 3 (depends on 1)

The affinity support according to claim 1, wherein the linker comprises an amino acid residue having an amino group or a thiol group at a terminal binding to the solid phase support.

### Claim 4 (depends on 1)

The affinity support according to claim 1, wherein the protein having the affinity to an immunoglobulin comprises an immunoglobulin-binding domain derived from an Fc-binding protein or Protein A.

### Claim 5 (depends on 1)

The affinity support according to claim 1,
wherein the protein having the affinity to an immunoglobulin comprises at least one immunoglobulin-binding domain selected from the group consisting of
an immunoglobulin-binding domain consisting of the amino acid sequence of SEQ ID NO: 3,
an immunoglobulin-binding domain comprising a partial sequence of the amino acid sequence of SEQ ID NO: 3, and
an immunoglobulin-binding domain consisting of an amino acid sequence having at least 70% identity to the amino acid sequence of SEQ ID NO: 3.

### Claim 6 (depends on 4)

The affinity support according to claim 4, wherein the protein having the affinity to an immunoglobulin comprises two or more of the immunoglobulin-binding domains.

### Claim 7 (depends on 1)

The affinity support according to claim 1, wherein the solid phase support comprises at least one reactive group capable of binding a thiol group or an amino group.

### Claim 8 (depends on 7)

The affinity support according to claim 7, wherein the at least one reactive group is an epoxy group.

### Claim 9 (depends on 1)

A method for isolating immunoglobulin, comprising:
isolating the immunoglobulin with the affinity support according to claim 1.

### Claim 10

An affinity ligand, comprising:
a linker R and
a protein ligand R1,
wherein
the linker R comprises a polyproline comprising from 12 to 24 proline residues,
R1 is a protein having an affinity to an immunoglobulin, and
R is bound to a C terminal or an N terminal of an amino acid sequence of the protein R1.
