Method for preventing deletion sequences in solid phase synthesis

• US 5,021,550 A
• Filed: 09/11/1990
• Issued: 06/04/1991
• Est. Priority Date: 10/07/1986
• Status: Expired due to Term

• Current Assignee: Thomas Jefferson University (Main Line Health System)
• Original Assignee: Thomas Jefferson University (Main Line Health System)
• Inventors: Zeiger, Allen R.
• Primary Examiner(s): Schain, Howard E.
• Assistant Examiner(s): PERKINS, SUSAN
• Application Number:
  US07/581,063
• Time in Patent Office: 266 Days
• Field of Search: 530/334, 530/333
• US Class Current: 530/334
• CPC Class Codes: C07H 21/00 Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
• CPC Class Codes: C07K 1/04 on carriers C07K1/003, C07K1/006 take precedence

Abstract

Improved methods for solid-state synthesis of polymers, especially polypeptides and polynucleotides, are provided. In accordance with a preferred embodiment, selectively activatable and reactive bonding moieties are covalently bonded to solid supports for polynucleotide and polypeptide syntheses. Products of failed reactions and some side products are caused to react with the selectively activatable and reactive bonding moiety to cause divalent bonding of unwanted products to the solid support. Upon cleavage of the initial situs of covalent bonding to the solid support, desired products are free to be collected while unwanted products remain covalently bonded to the support. Ease of purification of such polymers is a principal object of the present invention. The methods of the invention are amenable to automation and digital control and novel solid supports, activatable, reactive bonding moieties and other compositions are presented. The expression of polynucleotides prepared in accordance with preferred embodiments produces novel polypeptides.

Claims

1. A method of preparing a polypeptide comprising:

(a) providing an intermediate polypeptide having a carboxyl terminus and an amine terminus, convalently bound to a solid support at the carboxyl terminus of said intermediate polypeptide;

(b) reacting an amino acid moiety with the intermediate polypeptide under conditions selected to covalently bond the amino acid moiety with the intermediate polypeptide; and

(c) exposing the products of step (b) to reaction conditions selected to effect covalent bonding of at least a portion of any unreacted intermediate polypeptide remaining after step (b) with the solid support at the amine terminus of said intermediate polypeptide.

2. The method of claim 1 further comprising performing steps (b) and (c), sequentially, a plurality of times with a preselected series of amino acid moieties to produce a preselected polypeptide.

3. The method of claim 1 further comprising isolating the polypeptide thus prepared in substantially pure form.

4. The method of claim 3 wherein the isolation comprises cleaving the covalent bond at said carboxyl terminus under conditions which substantially do not cleave the covalent bond at the amine terminus.

5. The method of claim 1 wherein said solid support has selectively activatable bonding moieties bonded thereto.

6. The method of claim 5 wherein the selectively activatable bonding moieties comprise sarcosyl moieties.

7. The method of claim 6 wherein the exposing step comprises selectively activating the bonding moiety to form a species reactive with the intermediate polypeptide.

8. The method of claim 1 wherein the exposing step comprises reacting a free amino or carboxyl functionability on the unreacted intermediate polypeptide with an activating material to form a chemical species reactable with the solid support.

9. The method of claim 8 wherein the activating material is phosgene.

10. The method of claim 1 performed under autonomous control.

11. A method of preparing a polypeptide comprising:

providing a solid support;

bonding a first amino acid moiety having a carboxyl terminus and an amine terminus to the solid support through the carboxyl terminus;

reacting a series of further amino acid moieties with the first amino acid moiety bound to the solid support to form an intermediate polypeptide having a carboxyl terminus and an amine terminus covalently bound to the support at the carboxyl terminus of said intermediate polypeptide; and

reacting an additional amino acid moiety with the intermediate polypeptide under conditions selected to covalently bond the additional amino acid moiety with the intermediate polypeptide; and

exposing the products of the preceding step to reaction conditions selected to effect covalent bonding of at least a portion of any unreacted intermediate polypeptide remaining after the reaction of the preceding step with the solid support at the amine terminus of said intermediate polypeptide.