IP Library Granted Patent US 7,193,041
Granted Patent B2
US 7,193,041 · App. 09/839,696 · Granted Mar 20, 2007

Method for purification of recombinant proteins

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Quick Facts
Patent No.
US 7,193,041
App. No.
09/839,696
Granted
Mar 20, 2007
Kind
B2
Abstract

Purification of poly-amino acid-tagged recombinant proteins has been improved by the use of a carboxymethylated aspartate ligand complexed with a third-block transition metal having an oxidation state of 2 + and a coordination number of 6. A method for synthesizing the metal ion-CM-Asp complex is also described. Further, the metal ion-CM-Asp complex can be used for screening protein function.

Claims (21)

1. A method for synthesizing carboxymethylated aspartate agarose chelating resin, said method comprising:

(a) forming oxirane-agarose;

(b) conjugating aspartic acid to said oxirane-agarose to produce aspartate agarose, wherein said conjugating aspartic acid to said oxirane-agarose comprises reacting said oxirane-agarose and said aspartic acid at about 80° C. for 4 hours;

(c) carboxymethylating said aspartate agarose to produce carboxymethylated aspartate agarose; and

(d) complexing said carboxymethylated aspartate agarose with a metal ion other than Ca 2+ to produce a complex that offers two available valencies, wherein said metal ion is a transition metal ion.

2. The method, according to claim 1 , wherein said conditions for oxirane-agarose formation comprise carrying out the formation at about room temperature, overnight, adjusting to about pH 7.0.

3. The method, according to claim 1 , wherein said method further comprises washing said aspartate-agarose to remove extraneously bound metals.

4. The method according to claim 1 , wherein said transition metal ion is a third-block transition metal ion.

5. The method according to claim 4 , wherein said transition metal ion is selected from the group consisting of Fe 2+ , Co 2+ , Ni 2+ , Cu 2+ and Zn 2+ .

6. The method according to claim 5 , wherein said transition metal ion is Co 2+ .

7. The method according to claim 1 , wherein said transition metal is complexed to said carboxymethylated aspartate agarose in an octahedral geometry.

8. A method for synthesizing carboxymethylated aspartate agarose chelating resin, said method comprising:

(a) forming oxirane-agarose;

(b) conjugating aspartic acid to said oxirane-agarose to produce aspartate agarose, wherein said conjugating aspartic acid to said oxirane-agarose comprises reacting said oxirane-agarose and said aspartic acid at about 80° C. for 4 hours;

(c) carboxymethylating said aspartate agarose to produce carboxymethylated aspartate agarose; and

(d) complexing said carboxymethylated aspartate agarose with a metal ion other than Ca 2+ to produce a carboxymethylated aspartate agarose chelating resin described by the formula:

 wherein R 4 —R 5 —R 6 =H;

M=transition metal ion in a 2+ oxidation state with a coordination number of 6;

R 1 =a linking arm connecting the nitrogen atom of CM-Asp with R 2 ;

R 2 =a functional linking group through which CM-Asp linking arm R 1 is connected to R 3 ; and

R 3 =an agarose matrix.

Assignments (3)
CHANGE OF NAME Recorded Aug 4, 2016
From: CLONTECH LABORATORIES, INC.
To: TAKARA BIO USA, INC.
Reel/Frame 039584/0025 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2005
From: NELSON, PAUL S.; YANG, TE-TUAN; KAIN, STEVEN R.; SMITH, THOMAS H.
To: CLONTECH LABORATORIES, INC.
Reel/Frame 016903/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 3, 2005
From: NELSON, PAUL S.; YANG, TE-TUAN; KAIN, STEVEN R.
To: CLONTECH LABORATORIES, INC.
Reel/Frame 016729/0069 →