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Method for preparing synthetic peptide antigen 2600 of swine O-type foot and mouth disease through solid-phase fragment process

A technology for foot-and-mouth disease and synthesizing peptides, which can be used in the preparation methods of peptides, biochemical equipment and methods, chemical instruments and methods, etc., and can solve problems such as wrong sequences, unachievable yields, and pollution.

Active Publication Date: 2015-01-14
SHANGHAI SHEN LIAN BIOMEDICAL CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although a lot of research has been done on most of the possible side reactions and their mechanisms in the past few years, the yield of a single-step cycle still cannot reach more than 99.5%, and the remaining 0.5% of each step accumulates as by-products of polluting products.
Therefore, the target peptide is easily contaminated by a series of compounds with similar structures and chemical properties, such as diastereoisomers formed by epimerization, wrong sequences and incomplete core sequences, etc.

Method used

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  • Method for preparing synthetic peptide antigen 2600 of swine O-type foot and mouth disease through solid-phase fragment process
  • Method for preparing synthetic peptide antigen 2600 of swine O-type foot and mouth disease through solid-phase fragment process
  • Method for preparing synthetic peptide antigen 2600 of swine O-type foot and mouth disease through solid-phase fragment process

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0069] This embodiment relates to the preparation of SEQ ID No: 3 modified by 9-fluorenylmethoxycarbonyl at the amino end, comprising the following steps:

[0070] (1) Preparation of Fmoc-Pro-2-chlororityl resin

[0071] Weigh 100g of 2-chlororityl resin (100-200 mesh, 1.1mmol / g, 110mmol) into the EST-50 peptide synthesizer, swell with 1L of DCM for 30min, filter to dryness, add 1L of Fmoc-Pro-Pro- OH (110mmol) and 14.2g of DIEA (18.7ml, 110mmol of DCM solution, react at 20-25°C for 60min. Filter to dryness, add 1L of MeOH / DIEA (9:1) solution for blocking reaction for 30min, after filtration, the resins are sequentially Wash several times with NMP, MeOH, and NMP, and drain to obtain Fmoc-Pro-2-chlororityl resin. Take a small amount of resin and wash it several times with MeOH to measure the load by removing Fmoc method, and the measured load is 0.70mmol / g .

[0072] (2) Preparation of Fmoc-Leu-Pro-2-chlorotrityl resin

[0073] Add 1L of 20% piperidine / NMP to the resin in st...

Embodiment 2

[0079] This embodiment relates to the preparation of SEQ ID No: 4 modified by 9-fluorenylmethoxycarbonyl at the amino end, comprising the following steps:

[0080] (1) Preparation of Fmoc-Pro-2-chlororityl resin

[0081] Weigh 100g of 2-chlororityl resin (100-200 mesh, 1.1mmol / g, 110mmol) into the EST-50 polypeptide synthesizer, swell with 1L of DCM for 30min, filter to dryness, add 1L to dissolve 37.1g of Fmoc-Pro- OH (110mmol) and 14.2g of DIEA (18.7ml, 110mmol) in DCM were reacted at 20-25°C for 60min. After filtering to dryness, add 1L of MeOH / DIEA (9:1) solution to carry out blocking reaction for 30min. After filtering, the resin was washed several times with NMP, MeOH, and NMP in turn, and then drained to obtain Fmoc-Pro-2-chlorotrityl resin. Take a small amount of resin and wash it several times with MeOH to measure the loading by removing Fmoc method, and the measured loading is 0.70mmol / g.

[0082] (2) Preparation of Fmoc-Thr(tBu)-Pro-2-chlorotrityl resin

[0083] ...

Embodiment 3

[0089] This embodiment relates to the preparation of SEQ ID No: 5 modified by 9-fluorenylmethoxycarbonyl at the amino end, comprising the following steps:

[0090] (1) Preparation of Fmoc-Gly-2-chlororityl resin

[0091] Weigh 100g of 2-chlororityl resin (100-200 mesh, 1.1mmol / g, 110mmol) into the EST-50 peptide synthesizer, swell with 1L of DCM for 30min, filter to dryness, add 1L to dissolve 32.7g of Fmoc-Gly- OH (110mmol) and 14.2g of DIEA (18.7ml, 110mmol) in DCM were reacted at 20-25°C for 60min. After filtering to dryness, add 1L of MeOH / DIEA (9:1) solution for blocking reaction for 30min. After filtering, the resin was washed several times with NMP, MeOH, and NMP in sequence, and then drained to obtain Fmoc-Gly-2-chlorotrityl resin. Take a small amount of resin and wash it several times with MeOH to measure the loading by removing Fmoc method, and the measured loading is 0.65mmol / g.

[0092] (2) Preparation of Fmoc-Arg(Pbf)-Gly-2-chlorotrityl resin

[0093] Add 1L of...

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Abstract

The invention provides a method for preparing a synthetic peptide antigen 2600 of a swine O-type foot and mouth disease through a solid-phase fragment process. The method comprises the steps of with resin as a raw material, sequentially connecting 9-fluorenylmethoxycarbonyl protective amino acid to prepare a protected peptide fragment, meanwhile, sequentially removing a 9-fluorenylmethoxycarbonyl protecting group, carrying out linker reaction by using a condensing agent, and cutting off the protected peptide fragment by using dilute acid or weak acid; connecting the fragment and 4-(4'-dimethoxy-9-fluorenylmethoxyaminomethyl)-phenyloxymethyl resin step by step, and then, connecting the fragment and a T helper cell epitope; removing the protecting group and the resin by using concentrated acid or strong acid to obtain a crude peptide of the synthetic peptide antigen 2600; and purifying by using ion exchange resin and a tangential flow film packaging system, and removing small molecules and salt through a concentration system to obtain the synthetic peptide antigen 2600. The method provided by the invention has the characteristics of stable process, short production period, convenience in obtaining raw and auxiliary materials, few wastewater, waste gas and waste residues, low production cost, high yield and the like.

Description

technical field [0001] The invention relates to a method for preparing swine type O foot-and-mouth disease synthetic peptide antigen 2600 by a solid-phase fragment method. Background technique [0002] Structural formula of swine type O foot-and-mouth disease synthetic peptide antigen 2600: [0003] [0004] Pig foot-and-mouth disease is an acute, febrile, highly contagious infectious disease caused by foot-and-mouth disease virus. In recent years, foot-and-mouth disease has broken out in a large area in Jiangsu, Sichuan, the three northeastern provinces and Inner Mongolia, causing huge economic losses. Currently, immunization remains the main means of controlling the disease. The traditional inactivated vaccine is still the leading method for the prevention and treatment of foot-and-mouth disease at home and abroad, but it is easy to cause side effects such as allergies, and there are also problems in biosafety. Therefore, a lot of research has been done on new vaccin...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/09C07K1/36C07K1/34C07K1/18C07K1/06C07K1/04
CPCY02P20/55C07K14/005C12N2770/32122
Inventor 姬明放张震
Owner SHANGHAI SHEN LIAN BIOMEDICAL CORP
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