Methods and systems for solid phase peptide synthesis

Patent metadata

Field	Value
Publication number	US-11584776-B2
Application number	US-202016874824-A
Country	US
Kind code	B2
Filing date	May 15, 2020
Priority date	Sep 17, 2015
Publication date	Feb 21, 2023
Grant date	Feb 21, 2023

Abstract

Methods and systems for control of solid phase peptide synthesis are generally described. Control of solid phase peptide synthesis involves the use of feedback from one or more reactions and/or processes (e.g., reagent removal) taking place in the solid phase peptide synthesis system. In some embodiments, a detector may detect one or more fluids flowing across a detection zone of a solid phase peptide synthesis system and one or more signals may be generated corresponding to the fluid(s). For instance, an electromagnetic radiation detector positioned downstream of a reactor may detect a fluid exiting the reactor after a deprotection reactor and produce a signal(s). In some embodiments, based at least in part on information derived from the signal(s), a parameter of the system may be modulated prior to and/or during one or more subsequent reactions and/or processes taking place in the solid phase peptide synthesis system. In some embodiments, the methods and systems, described herein, can be used to conduct quality control to determine and correct problems (e.g., aggregation, truncation, deletion) in reactions (e.g., coupling reactions) taking place in the solid phase peptide synthesis system.

First claim

What is claimed is:

1. A method of operating a peptide synthesis system, comprising:
performing a first amino acid addition cycle of a first peptide synthesis process to synthesize a peptide on a solid support in a reactor, the first amino acid addition cycle comprising a first deprotection reaction, a first coupling reaction, and one or more first optional reagent removal steps;
detecting, during the first amino acid addition cycle of the first peptide synthesis process, an electromagnetic absorbance and/or an electromagnetic emission of a fluid stream at a detection zone positioned downstream of the reactor to produce a reference signal comprising a reference peak;
performing a second amino acid addition cycle of the first peptide synthesis process or of a second peptide synthesis process, the second amino acid addition cycle comprising a second deprotection reaction, a second coupling reaction, and one or more second optional reagent removal steps;
detecting, during the second amino acid addition cycle, an electromagnetic absorbance and/or an electromagnetic emission of a fluid stream at the detection zone positioned downstream of the reactor to produce a signal comprising a first peak;
determining whether improper resin loading and/or a mechanical failure has occurred during the second coupling reaction based at least in part on a comparison between a property of the first peak and a corresponding property of a reference peak; and
stopping the peptide synthesis process that included the second amino acid addition cycle and starting a subsequent peptide synthesis process if the comparison indicates that improper resin loading and/or a mechanical failure has occurred during the second coupling reaction.

2. The method of claim 1 , wherein the first coupling reaction is between an amino acid and an immobilized amino acid residue.

3. The method of claim 1 , wherein the electromagnetic absorbance and/or the electromagnetic emission is selected from a group consisting of infrared absorbance, infrared emission, ultraviolet absorbance, and/or ultraviolet emission.

4. The method of claim 1 , wherein the determining comprises comparing an area of the first peak to an area of the reference peak.

5. The method of claim 1 , wherein the determining comprises determining whether improper resin loading and/or a mechanical failure has occurred during a coupling reaction based at least in part on a comparison between a property of the first peak, a corresponding property of the reference peak, and a corresponding property of a second reference peak that is part of a signal generated during an additional amino acid addition cycle.

6. The method of claim 5 , wherein the determining comprises:
determining that each of an area of the first peak, an area of the reference peak, and an area of the second reference peak are below a value; and
determining that a width of the first peak, a width of the reference peak, and a width of the second reference peak are of a consistent size.

7. The method of claim 1 , wherein the detecting, during the first amino acid addition cycle, comprises detecting an electromagnetic absorbance of the fluid stream at the detection zone.

8. A method of operating a peptide synthesis system, comprising:
performing a first amino acid addition cycle of a first peptide synthesis process to synthesize a peptide on a solid support in a reactor, the first amino acid addition cycle comprising a first deprotection reaction, a first coupling reaction, and one or more first optional reagent removal steps;
detecting, during the first amino acid addition cycle of the first peptide synthesis process, an electromagnetic absorbance and/or an electromagnetic emission of a fluid stream at a detection zone positioned downstream of the reactor to produce a reference signal comprising a reference peak;
performing a second amino acid addition cycle of the first peptide synthesis process or of a second peptide synthesis process, the second amino acid addition cycle comprising a second deprotection reaction, a second coupling reaction, and one or more second optional reagent removal steps;
detecting, during the second amino acid addition cycle, an electromagnetic absorbance and/or an electromagnetic emission of a fluid stream at the detection zone positioned downstream of the reactor to produce a signal comprising a first peak;
comparing a property of the first peak and a corresponding property of the reference peak; and
based at least in part on the comparing, stopping the peptide synthesis process that included the second amino acid addition cycle and/or performing at least one of the following during a coupling reaction of a subsequent peptide synthesis process to synthesize the peptide, the coupling reaction of the subsequent peptide synthesis process corresponding to the coupling reaction of the peptide synthesis process that included the second amino acid addition cycle:
increasing a residence time of an activating agent; and/or
employing a different activating agent; and/or
increasing a temperature of the reactor and/or the fluid stream; and/or
employing a different stoichiometric ratio.

9. The method of claim 8 , wherein the property of the first peak is an area of the first peak and the corresponding property of the reference peak is an area of the reference peak.

10. The method of claim 8 , wherein the property of the first peak is a height of the first peak and the corresponding property of the reference peak is a height of the reference peak.

11. The method of claim 8 , wherein the property of the first peak is a width of the first peak and the corresponding property of the reference peak is a width of the reference peak.

12. The method of claim 8 , comprising:
determining that each of an area of the first peak, an area of the reference peak, and an area of a second reference peak that is part of a signal generated during an additional amino acid addition cycle are below a value;
determining that a width of the first peak, a width of the reference peak, and a width of the second reference peak are of a consistent size; and
subsequently stopping the peptide synthesis process that included the second amino acid addition cycle and starting a subsequent peptide synthesis process.

13. The method of claim 8 , comprising:
determining that each of an area of the reference peak and an area of a second reference peak that is part of a signal generated during an additional amino acid addition cycle are above a value while an area of the first peak is below the value;
determining that a width of the first peak, a width of the reference peak, and a width of the second reference peak are of a consistent size; and
subsequently, stopping the peptide synthesis process that included the second amino acid addition cycle and/or performing at least one of the following during a coupling reaction of a subsequent peptide synthesis process to synthesize the peptide having the sequence, the coupling reaction of the subsequent peptide synthesis process corresponding to the coupling reaction of the peptide synthesis process that included the second amino acid addition cycle:
increasing a residence time of an activating agent; and/or
employing a more reactive activating agent.

14. The method of claim 13 , comprising:
stopping the peptide synthesis process that included the second amino acid addition cycle and starting a subsequent peptide synthesis process to synthesize the peptide if a change in area between the first peak and the reference peak is greater than 20%.

15. The method of claim 8 , comprising:
determining th

Assignees

• Massachusetts Inst Technology

Inventors

• Thomas Iii Dale Arlington
• Mijalis Alexander James
• Pentelute Bradley L
• Simon Mark David
• Mong Surin

Classifications

• C07K14/61

  Growth hormone [GH], i.e. somatotropin · CPC title

• G01N2021/8416

  and process controlling, not otherwise provided for · CPC title

• C07K1/045 Primary

  using devices to improve synthesis, e.g. reactors, special vessels · CPC title

• G01N21/3577

  for analysing liquids, e.g. polluted water · CPC title

• G01N21/272

  for following a reaction, e.g. for determining photometrically a reaction rate (photometric cinetic analysis) · CPC title