阅读说明：本技术 一种筛选新冠病毒主蛋白酶小分子抑制剂的方法及筛选模型 (Method and screening model for screening new coronavirus main protease small-molecule inhibitor ) 是由 陈云雨 司书毅 张晶 闫干干 李东升 李妍 许艳妮 陈明华 刘超 李顺旺 王晨吟 于 2021-07-01 设计创作，主要内容包括：本发明涉及一种筛选新冠病毒主蛋白酶(main protease,Mpro)小分子抑制剂的方法及筛选模型。该方法及筛选模型基于荧光偏振(fluorescence polarization)原理,以荧光探针FITC-Substrate-Biotin作为新冠病毒Mpro的水解底物,再以亲和素(avidin)终止其水解反应,以多功能酶标仪检测实验体系的毫偏值(millipolarization units,mP)。活性化合物在本筛选模型中表现较高的mP值,非活性化合物则表现较低的mP值。(The invention relates to a method for screening a novel coronavirus main protease (Mpro) small-molecule inhibitor and a screening model. The method and the screening model are based on the principle of fluorescence polarization, a fluorescent probe FITC-Substrate-Biotin is used as a hydrolysis Substrate of the Mpro of the new coronavirus, the hydrolysis reaction is stopped by avidin (avidin), and the millipolarization units (mP) of an experimental system are detected by a multifunctional microplate reader. Active compounds exhibit higher mP values in this screening model, while inactive compounds exhibit lower mP values.)

1. A method for screening for a novel small molecule inhibitor of main protease (Mpro) of coronavirus, said method comprising the steps of:

(1) preparing high-activity Mpro recombinant protein by using an escherichia coli prokaryotic expression method;

(2) adding a compound to be screened and an Mpro recombinant protein for incubation;

preferably, in the step (2), the Mpro recombinant protein solution (the concentration of the Mpro recombinant protein is 100-2000 nM) and the compound to be screened (the concentration is 1-5 mM) are mixed in proportion and incubated for 20-60 min at room temperature;

(3) taking Fluorescein Isothiocyanate (FITC) and a Biotin-labeled FITC-Substrate-Biotin polypeptide (FITC-S-Biotin: FITC-AVLQSGFRKK-Biotin) as Mpro hydrolysis substrates, and incubating for 5-60 min at room temperature;

preferably, in the step (3), the concentration of the FITC-S-Biotin is 20-100 nM, and the volume of the added FITC-S-Biotin solution is 1/2-1/1 (v/v) of the system in the step (2). Adding FITC-S-Biotin, and incubating at room temperature for 5-40 min;

(4) terminating the hydrolysis reaction by avidin, incubating for 1-30 min at room temperature, and detecting the mP value by a multifunctional enzyme-labeling instrument;

preferably, in the step (4), the concentration of the avidin is 10-500 nM, and the volume of the avidin solution added is 1/6-1/1 (v/v) of the system in the step (2). After adding the avidin, incubating at room temperature for 1-10 min, and detecting the mP value by using a multifunctional enzyme-labeling instrument;

(5) drawing an inhibition curve of the target compound, and calculating the IC of the target compound on the new coronavirus main protease₅₀A value;

the amino acid sequence of the new coronavirus main protease is shown as SEQ ID NO. 2.

2. The method of claim 1,

in the step (2): after mixing the solution of Mpro recombinant protein (Mpro recombinant protein concentration 400nM) with the compound to be screened (concentration 3mM) in the ratio of 1:29(v/v), incubation was carried out for 40min at room temperature.

3. The method of claim 1,

in the step (3): the FITC-S-Biotin concentration was 60nM, and the volume of FITC-S-Biotin solution added was 2/3(v/v) for the system of step (2). After addition of FITC-S-Biotin, incubation was carried out for 20min at room temperature.

4. The method of claim 1,

in the step (4): the avidin concentration was 300nM and the volume of avidin solution added was 1/3(v/v) for the system of step (2). After adding the avidin, the mixture is incubated for 5min at room temperature, and the mP value is detected by a multifunctional microplate reader.

5. The method of claim 1,

the method for preparing the high-activity Mpro recombinant protein by the escherichia coli prokaryotic expression method in the step (1) comprises the following steps:

connecting an Mpro gene fragment with a nucleotide sequence shown as SEQ ID NO.1 to a pET-21a (+) expression vector to construct a recombinant plasmid Mpro-pET-21 a;

secondly, the recombinant plasmid is transformed into E.coli Rosetta (DE3) competent cells for Mpro soluble expression, and the new coronavirus Mpro recombinant protein is separated and purified by a HisTrap affinity chromatography column.

6. The method according to any one of claims 1 to 5,

in the step of drawing an inhibition curve of the target compound in the step (5), the calculation formula of the inhibition rate is as follows:

。

7. a fluorescence polarization screening kit for screening a new coronavirus main protease small molecule inhibitor, wherein the kit comprises:

(1) detecting effective amount of Mpro recombinant protein of the new coronavirus, a fluorescent probe FITC-S-Biotin and avidin;

(2) necessary solvents and reagents.

8. The use of the fluorescence polarization screening kit for screening a novel coronavirus main protease small molecule inhibitor as claimed in claim 7 in screening a novel coronavirus main protease small molecule inhibitor.

Technical Field

The invention belongs to the technical field of medical biology, and particularly relates to a method for screening a novel coronavirus main protease small-molecule inhibitor and a screening model.

Background

The rapid development of novel coronavirus (SARS-CoV-2) vaccine, humanized antibody and anti-new coronavirus medicine has become a significant scientific problem faced by the scientific community. Despite significant advances in the development of new coronavirus vaccines, safe and effective broad-spectrum anti-new coronavirus drugs are also of paramount importance for unvaccinated individuals or situations where high-frequency genetic mutations in the virus lead to decreased vaccine protection (Wang Z, et al nature, 2021). Although some candidate antiviral drugs have been used for clinical treatment, such as Reidesvir, Favipiravir, ribavirin, telbivudine, etc., all show limited or ineffective efficacy in large-scale clinical trials, it is of great importance to actively develop novel broad-spectrum anti-new coronavirus drugs.

The current research shows that the evolved highly conserved main protease (Mpro) of the new coronavirus has important biological functions in regulating and controlling the RNA replication of the new coronavirus, and a human body lacks of the protease homologous with the Mpro, so that the main protease becomes one of ideal targets for developing novel broad-spectrum anti-coronavirus medicaments (Morse JS, et al. Chemiochemchem, 2020; Jin Z, et al. Nature, 2020; Jin Z, et al. biochem Biophys Res Commun, 2021). In the development process of the high-selectivity new coronavirus Mpro small-molecule inhibitor, the establishment of a simple, rapid, sensitive and economic drug high-throughput screening model is an important basis and key technology (Hippocampus, et al., chemistry of Life, 2021) for efficient screening and development. Methods for screening for Mpro small molecule inhibitors that have been reported so far mainly include virtual screening, Fluorescence Resonance Energy Transfer (FRET), luciferase reporter screening, green fluorescent protein cleavage complementation, phenotypic screening, etc. (Li Z, et al. Proc Natl Acad Sci USA, 2020; Zhu W, et al. ACS Pharmacol Transl Sci, 2020; Coelho C, et al. PLoS One, 2020; Hung HC, et al. Antimicrob Agents Chemothers, 2020; Malaysia, et al. pharmaceutical reports, 2020; Rawson J, et al. Virus, 2021; Froggatt, et al. J Virol, 2020; Rothan HA, et al. mol Biotechnol, 2021; Riva L, et al. Nature, 2020). However, the above-mentioned screening methods generally have the disadvantages of high false positive rate, high screening cost, complicated operation, poor stability, long screening period, etc., and thus the application thereof in large-scale high-throughput screening is greatly limited (chiffon, et al, chemical of life, 2021). Therefore, the active development of a novel high-throughput screening model of the Mpro small-molecule inhibitor, which is simple, rapid, sensitive and economical, is of great significance.

Disclosure of Invention

The invention firstly relates to a method for screening a novel coronavirus main protease small-molecule inhibitor, which comprises the following steps:

(1) the high-activity Mpro recombinant protein is prepared by an escherichia coli prokaryotic expression method.

(2) Adding the compound to be screened and incubating with the Mpro recombinant protein.

Preferably, the solution of Mpro recombinant protein (the concentration of the Mpro recombinant protein is 100-2000 nM) and the compound to be screened (the concentration is 1-5 mM) are mixed in proportion and incubated for 20-60 min at room temperature.

More preferably, the solution of the Mpro recombinant protein (Mpro recombinant protein concentration is 400nM) is mixed with the compound to be screened (concentration is 3mM) in a ratio of 1:29(v/v) and incubated at room temperature for 40 min.

(3) Fluorescein Isothiocyanate (FITC) and a Biotin-labeled FITC-Substrate-Biotin polypeptide (FITC-S-Biotin: FITC-AVLQSGFRKK-Biotin) are used as Mpro hydrolysis substrates and are incubated for 5-60 min at room temperature.

Preferably, the concentration of the FITC-S-Biotin is 20-100 nM, and the volume of the added FITC-S-Biotin solution is 1/2-1/1 (v/v) of the system in the step (2). After adding FITC-S-Biotin, incubating at room temperature for 5-40 min.

More preferably, the FITC-S-Biotin concentration is 60nM and the volume of FITC-S-Biotin solution added is 2/3(v/v) of the system of step (2). After addition of FITC-S-Biotin, incubation was carried out for 20min at room temperature.

(4) And (3) terminating the hydrolysis reaction by using avidin, incubating for 1-30 min at room temperature, and detecting the mP value by using a multifunctional enzyme-labeling instrument.

Preferably, the concentration of the avidin is 10-500 nM, and the volume of avidin solution added is 1/6-1/1 (v/v) of the system of step (2). And (3) after adding the avidin, incubating at room temperature for 1-10 min, and detecting the mP value by using a multifunctional enzyme-labeling instrument.

More preferably, the avidin concentration is 300nM and the volume of avidin solution added is 1/3(v/v) for the system of step (2). After the addition of avidin, the incubation was carried out at room temperature for 5min, and the mP value was measured with a multifunctional microplate reader.

(5) Drawing an inhibition curve of the target compound, and calculating the IC of the target compound on the new coronavirus main protease₅₀The value is obtained.

The method for preparing the high-activity Mpro recombinant protein by the escherichia coli prokaryotic expression method in the step (1) comprises the following steps:

connecting a codon-optimized Mpro gene to a pET-21a (+) expression vector to construct a recombinant plasmid Mpro-pET-21 a;

secondly, the recombinant plasmid is transformed into E.coli Rosetta (DE3) competent cells for Mpro soluble expression, and the new coronavirus Mpro recombinant protein is separated and purified by a HisTrap affinity chromatography column.

In the step of drawing an inhibition curve of the target compound in the step (5), the calculation formula of the inhibition rate is as follows:

the invention also relates to a fluorescence polarization screening kit for screening the new coronavirus main protease small-molecule inhibitor, which comprises the following components in part by weight:

(1) detecting effective amount of Mpro recombinant protein of the new coronavirus, a fluorescent probe FITC-S-Biotin and avidin;

(2) necessary solvents and reagents.

The invention also relates to application of the fluorescence polarization screening kit for screening the new coronavirus main protease small molecule inhibitor in screening the new coronavirus main protease small molecule inhibitor.

The invention has the following beneficial effects:

the invention discloses a fluorescence polarization high-throughput screening model for screening a novel coronavirus main protease small-molecule inhibitor and a using method thereof, belonging to the technical field of medical biology. The high-throughput screening model is based on a fluorescence polarization principle, takes a fluorescence probe FITC-S-Biotin as a hydrolysis substrate of the Mpro of the new coronavirus, then stops the hydrolysis reaction by avidin, and detects the mP value of an experimental system by a multifunctional microplate reader. The active compounds show higher mP values in this screening model, while the inactive compounds show lower mP values. The method specifically comprises the following steps:

(1) the fluorescence polarization high-throughput screening model established by the invention is suitable for rapid screening, discovery and activity evaluation of anti-new coronavirus medicines taking main protease as a target;

(2) the fluorescence polarization high-throughput screening model established by the invention has the advantages of homogeneous reaction, simple and convenient operation, sensitive detection, low cost and the like;

(3) the fluorescence polarization high-throughput screening model established by the invention is not limited to high-throughput screening of the main protease small-molecule inhibitor of the new coronavirus, and key protease small-molecule inhibitors for regulating and controlling virus replication in other pathogenic viruses can be applied or improved to carry out rapid screening and discovery.

Drawings

FIG. 1 shows codon-optimized sequences and amino acid sequences of the recombinant protein Mpro of the novel coronavirus in example 1 of the present invention.

FIG. 2, prokaryotic expression, separation and purification and biological activity identification of recombinant protein of Mpro of new coronavirus in example 1 and example 2 of the present invention. 2A, prokaryotic expression, separation and purification of a new coronavirus Mpro recombinant protein: lane M protein standard molecular weight; lane 1, mycoprotein; swimming lane 2, cracking the supernatant; lane 3 crude extract; lane 4 purified Mpro recombinant protein. 2B: a standard curve of the fluorescence intensity of the MCA standard substance; 2C: fluorescence intensity curves after hydrolysis of MCA substrate by Mpro recombinant protein at different concentrations.

FIG. 3 is the reaction curve of recombinant proteolytic FITC-S-Biotin substrate of new coronavirus Mpro in example 3 of the present invention.

FIG. 4 shows the dose-response curve and IC of GC-376 in the fluorescence polarization high-throughput screening model in example 4 of the present invention₅₀The value is obtained.

FIG. 5 is a Z factor value of the fluorescence polarization high throughput screening model in example 5 of the present invention.

FIG. 6 shows dose-response curves and ICs of Rhus verniciflua Stokes and ginkgolic acid in fluorescence polarization high-throughput screening model in example 6 of the present invention₅₀The value is obtained.

Detailed Description

Unless otherwise indicated, the techniques used in the practice are conventional biochemical methods well known to those skilled in the art, and the reagents and materials used are commercially available.

Example 1 prokaryotic expression and isolation and purification of recombinant protein of Mpro of New coronavirus

The Mpro gene (figure 1) optimized by codon is connected to pET-21a (+) expression vector by using the prokaryotic expression technology of escherichia coli to construct a recombinant plasmid Mpro-pET-21 a. The recombinant plasmid was transformed into E.coli Rosetta (DE3) competent cells, and the recombinants were selected for ampicillin resistance. The recombinants were inoculated into 1 liter of LB liquid medium (containing 100. mu.g/mL ampicillin), cultured at 37 ℃ for 7 hours, added with 0.2mM IPTG, and induced at 30 ℃ for 8 hours. After the thalli is broken by an ultrasonic method, the cracked supernatant is separated and purified by a HisTrap affinity chromatography column, the apparent molecular weight of the purified Mpro is 34kDa, only one formylmethionine remains at the amino terminal, a polyhistidine tag is fused at the carboxyl terminal, the electrophoretic purity is more than 90 percent, and the concentration is 3 mg/mL (figure 1 and figure 2A).

The sequence of the codon-optimized Mpro gene is shown in SEQ ID NO.1, and the used enzyme cutting sites are Nde I (CATATG) and Xho I (CTCGAG). The Mpro recombinant protein contains a formylmethionine (fMet) at the amino terminal and a polyhistidine tag at the carboxyl terminal.

SEQ ID NO.1：

CATATGAGTGGCTTTCGTAAAATGGCCTTTCCGAGCGGCAAAGTTGAAGGTTGTATGGTGCAGGTGAC CTGCGGTACCACCACCCTGAATGGTCTGTGGCTGGATGATGTGGTTTATTGCCCGCGTCATGTGATTTG TACCAGTGAAGATATGCTGAATCCGAATTATGAAGATCTGCTGATTCGCAAAAGCAATCATAATTTTCT GGTGCAGGCCGGCAATGTTCAGCTGCGCGTGATTGGCCATAGTATGCAGAATTGCGTTCTGAAACTGA AAGTGGATACCGCAAATCCGAAAACCCCGAAATATAAATTTGTTCGCATTCAGCCGGGTCAGACCTTT AGCGTGCTGGCATGTTATAATGGTAGTCCGAGCGGTGTGTATCAGTGCGCAATGCGTCCGAATTTTACC ATTAAGGGCAGTTTTCTGAATGGTAGCTGCGGCAGCGTTGGTTTTAATATTGATTATGATTGCGTGAGT TTCTGCTATATGCATCACATGGAACTGCCGACCGGTGTGCATGCAGGCACCGATCTGGAAGGTAATTTT TATGGCCCGTTTGTGGATCGCCAGACCGCACAGGCAGCCGGTACCGATACCACCATTACCGTTAATGT TCTGGCATGGCTGTATGCAGCCGTTATTAATGGTGACCGTTGGTTTCTGAATCGTTTTACCACCACCTT AAATGATTTTAATCTGGTTGCCATGAAGTATAATTACGAACCGCTGACCCAGGATCATGTGGATATTCT GGGCCCGCTGAGTGCCCAGACCGGTATTGCAGTTCTGGATATGTGTGCAAGCCTGAAAGAACTGCTG CAGAATGGTATGAATGGTCGTACCATTCTGGGTAGTGCACTGCTGGAAGATGAATTCACTCCGTTTGAT GTTGTGCGCCAGTGTAGCGGTGTGACCTTTCAGCTCGAG

The coded amino acid sequence is shown as SEQ ID NO.2,

SEQ ID NO.2：

MSGFRKMAFPSGKVEGCMVQVTCGTTTLNGLWLDDVVYCPRHVICTSEDMLNPNYEDLLIRKSNH NFLVQAGNVQLRVIGHSMQNCVLKLKVDTANPKTPKYKFVRIQPGQTFSVLACYNGSPSGVYQCAMRP NFTIKGSFLNGSCGSVGFNIDYDCVSFCYMHHMELPTGVHAGTDLEGNFYGPFVDRQTAQAAGTDTTIT VNVLAWLYAAVINGDRWFLNRFTTTLNDFNLVAMKYNYEPLTQDHVDILGPLSAQTGIAVLDMCASLKE LLQNGMNGRTILGSALLEDEFTPFDVVRQCSGVTFQLEHHHHHH

example 2 identification of the biological Activity of the Mpro recombinant protein of the New coronavirus

1. mu.M MCA (7-methoxycoumarin, 7-methoxycoumarin-4-acetic acid, MCA) was diluted in TBS solution (50mM Tris, 150mM NaCl pH8.0) in 5 concentration gradients by a 2-fold ratio, and wells containing only TBS solution were used as negative control wells. The above-mentioned MCA dilution was added to 384-well plates at 50. mu.L/well, and the total amount of MCA in each well was 0, 31.25, 62.5, 125, 250, and 500pmol, respectively, and the relative fluorescence intensity (RFU) was measured by a multifunctional microplate reader in an automatic gain mode. Based on the total MCA and Δ RFU values (Δ RFU ═ RFU) for each well_MCA-RFU₀) The regression equation was fitted and a calibration curve of MCA fluorescence intensity was plotted (FIG. 2B).

2. 2mM MCA-Substrate (MCA-AVLQSGFR-Lys (Dnp) -Lys-NH)₂) TBS solution was diluted to 10. mu.M, and Mpro was added to give final concentrations of 0, 0.25, 0.5 and 1. mu.M, respectively. The reaction solution is added into a 384-pore plate at a concentration of 50 mu L/pore, the gain value is set to be 58, the detection temperature is 25 ℃, the excitation light is 320nm, the emission light is 405nm, the detection interval is 1s, the total detection time is 3min, and the RFU value is detected by a multifunctional microplate reader. Within 30s of hydrolysis reaction time, T₁And T₂The RFU values at the time points are recorded as RFU respectively_T1And RFU_T2Calculating Δ RFU ═ RFU_T2-RFU_T1At Δ T ═ T, calculated from the standard curve of fig. 2B₂-T₁The total amount of MCA-AVLQ product produced by hydrolysis of MCA-Substrate by Mpro over time (pmol). Vitality unit (U) definition: in a hydrolysis reaction at 25 ℃ and pH8.0, Mpro hydrolyzes MCA-Substrate per minute to 1pmol MCA-AVLQ (product, P).

Using formula 2, the specific activity of purified Mpro was calculated to be not less than 50000U/mg (FIG. 2C).

Example 3 hydrolysis of FITC-S-Biotin substrate by recombinant protein of Mpro of New coronavirus

2mM FITC-S-Biotin is diluted to 60nM by fluorescence polarization reaction solution (10mM Tris,50mM NaCl,1mM DTT pH8.0), 20 muL/hole is added into a 384-hole plate, 0, 25, 50, 100, 150, 175, 200, 300, 400, 500, 600 and 700nM MPro are sequentially added into the plate, each hole is 30 muL, each group is provided with 3 groups of multiple holes, the plate is incubated for 20min at room temperature, 300nM avidin reaction solution is added into the plate at 10 muL/hole, the plate is incubated for 5min at room temperature without light, and the mP value is detected by a multifunctional microplate reader.

The Mpro hydrolysis reaction curve shows that 200nM Mpro can sufficiently hydrolyze FITC-S-Biotin substrate to the product FITC-AVLQ after incubation for 20min at room temperature (FIG. 3).

Example 4 inhibitory Activity of GC-376 in a fluorescence polarization high throughput screening model

GC-376 is a novel small molecule inhibitor of coronavirus Mpro, which has been reported to have good activity at present (FIG. 4A). 10mM GC-376 was diluted 2-fold at 400nM MPro (starting concentration 2. mu.M, 8 concentration gradients total dilution) and added to 384-well plates at 30. mu.L per well, with 3 duplicate wells per set, and incubated at room temperature for 40 min. Then 60nM FITC-S-Biotin was added to 384 well plates in sequence, 20. mu.L per well, and incubated at room temperature in the dark for 20 min. Then, 300nM avidin reaction solution was added continuously at 10. mu.L/well, and incubation was continued for 5min at room temperature, and the mP value was measured with a multifunctional microplate reader.

The negative well was set to Mpro (400nM, 29. mu.L/well) + DMSO (1. mu.L/well) + FITC-S-Biotin (60nM, 20. mu.L/well) + avidin (300nM, 10. mu.L/well), the positive well was set to fluorescence polarization reaction (29. mu.L/well) + DMSO (1. mu.L/well) + FITC-S-Biotin (60nM, 20. mu.L/well) + avidin (300nM, 10. mu.L/well), the inhibition curve of GC-376 was fitted and its IC was calculated₅₀The value is obtained.

Using equation 3, the IC of GC-376 in the fluorescence polarization screening model was calculated₅₀The value was 0.127. mu.M (FIG. 4B), which is the IC reported in the FRET screening model₅₀The values are basically consistent (Vuong W, et al. nat Commun,2020), which indicates that the established fluorescence polarization high-throughput screening model has good characteristicsAnd (3) different in nature.

Example 5 fluorescence polarization high throughput screening model Z factor values

The factor Z is a core parameter for evaluating the stability of a drug high-throughput screening model. By using a multifunctional microplate reader, the value of the Z factor of the fluorescence polarization high-flux screening model is calculated to be 0.85, and the basic requirement that the Z factor in the high-flux screening model is more than 0.5 is met (figure 5).

Example 6 use of fluorescence polarization high throughput screening model

The initial screening concentration of the compound library is 1mg/mL, 1 μ L of the compound and 400nM MPro (29 μ L/well) are added into a 384-well plate, after incubation for 40min at room temperature, 60nM FITC-S-Biotin is added, 20 μ L of each well, incubation for 20min at room temperature is continued, 300nM avidin (10 μ L/well) is added, and incubation for 5min at room temperature is continued. A negative control group (DMSO well) and a positive control group (GC-376 well, 1 mu M) are arranged at the same time, and the mP value is detected by a multifunctional microplate reader. Performing high-throughput screening on a natural product compound library by using an established fluorescence polarization high-throughput screening model, successfully screening that the fistulinic acid (AA) and Ginkgolic Acid (GA) have good inhibitory activity, and calculating the IC of the fistulinic acid (AA) and Ginkgolic Acid (GA) by using a formula 1₅₀The values were 9.62 and 7.15. mu.M, respectively (FIGS. 6A and 6B). At present, researches prove that the anacardic acid and the ginkgolic acid are small-molecule inhibitors of Mpro of the new coronavirus and have good antiviral activity on the new coronavirus (Xiong Y, et al. Fitoterapia, 2021; Chen Z, et al. cell Biosci, 2021), which also proves that the fluorescence polarization high-throughput screening model has good practicability and popularization.

Although the invention has been described in detail with respect to the general description and the specific embodiments thereof, it will be apparent that further improvements and modifications may be made by those skilled in the art based on the present invention. Therefore, any modification or improvement made on the basis of the fluorescence polarization principle or establishment and use of a fluorescence polarization high-throughput screening model of a key protease small molecule inhibitor for regulating and controlling virus replication in other pathogenic viruses belong to the protection scope of the invention. The FITC-S-Biotin substrate applied in the invention is not limited to the polypeptide sequence in the application embodiment for carrying out FITC and Biotin double labeling, and all Mpro substrate polypeptides containing an Mpro conserved cleavage sequence (L-Q-S/A) and other fluorescent molecular labels or synthesized by other amino acid modification technologies also belong to the protection scope of the invention. In addition, the new coronavirus Mpro applied in the invention is not limited to be prepared by using an Escherichia coli prokaryotic expression technology, but the preparation of Mpro by using yeast cells, CHO cells, insect cells, plant cells and other eukaryotic expression systems is also feasible, but the high-activity Mpro has a structure described herein, only one formylmethionine residue or a free amino terminal is left at the amino terminal, a polyhistidine tag at the carboxyl terminal can be optional, the influence on the biological activity of Mpro is small, and the construction strategy of Mpro also belongs to the protection scope of the invention.

SEQUENCE LISTING

<110> institute of medical and Biotechnology of Chinese academy of medical sciences

<120> method for screening new coronavirus main protease small molecule inhibitor and screening model

<130> CP121020635C

<160> 2

<170> PatentIn version 3.3

<210> 1

<211> 930

<212> DNA

<213> Artificial sequence

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catatgagtg gctttcgtaa aatggccttt ccgagcggca aagttgaagg ttgtatggtg 60

caggtgacct gcggtaccac caccctgaat ggtctgtggc tggatgatgt ggtttattgc 120

ccgcgtcatg tgatttgtac cagtgaagat atgctgaatc cgaattatga agatctgctg 180

attcgcaaaa gcaatcataa ttttctggtg caggccggca atgttcagct gcgcgtgatt 240

ggccatagta tgcagaattg cgttctgaaa ctgaaagtgg ataccgcaaa tccgaaaacc 300

ccgaaatata aatttgttcg cattcagccg ggtcagacct ttagcgtgct ggcatgttat 360

aatggtagtc cgagcggtgt gtatcagtgc gcaatgcgtc cgaattttac cattaagggc 420

agttttctga atggtagctg cggcagcgtt ggttttaata ttgattatga ttgcgtgagt 480

ttctgctata tgcatcacat ggaactgccg accggtgtgc atgcaggcac cgatctggaa 540

ggtaattttt atggcccgtt tgtggatcgc cagaccgcac aggcagccgg taccgatacc 600

accattaccg ttaatgttct ggcatggctg tatgcagccg ttattaatgg tgaccgttgg 660

tttctgaatc gttttaccac caccttaaat gattttaatc tggttgccat gaagtataat 720

tacgaaccgc tgacccagga tcatgtggat attctgggcc cgctgagtgc ccagaccggt 780

attgcagttc tggatatgtg tgcaagcctg aaagaactgc tgcagaatgg tatgaatggt 840

cgtaccattc tgggtagtgc actgctggaa gatgaattca ctccgtttga tgttgtgcgc 900

cagtgtagcg gtgtgacctt tcagctcgag 930

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Met Ser Gly Phe Arg Lys Met Ala Phe Pro Ser Gly Lys Val Glu Gly

1 5 10 15

Cys Met Val Gln Val Thr Cys Gly Thr Thr Thr Leu Asn Gly Leu Trp

20 25 30

Leu Asp Asp Val Val Tyr Cys Pro Arg His Val Ile Cys Thr Ser Glu

35 40 45

Asp Met Leu Asn Pro Asn Tyr Glu Asp Leu Leu Ile Arg Lys Ser Asn

50 55 60

His Asn Phe Leu Val Gln Ala Gly Asn Val Gln Leu Arg Val Ile Gly

65 70 75 80

His Ser Met Gln Asn Cys Val Leu Lys Leu Lys Val Asp Thr Ala Asn

85 90 95

Pro Lys Thr Pro Lys Tyr Lys Phe Val Arg Ile Gln Pro Gly Gln Thr

100 105 110

Phe Ser Val Leu Ala Cys Tyr Asn Gly Ser Pro Ser Gly Val Tyr Gln

115 120 125

Cys Ala Met Arg Pro Asn Phe Thr Ile Lys Gly Ser Phe Leu Asn Gly

130 135 140

Ser Cys Gly Ser Val Gly Phe Asn Ile Asp Tyr Asp Cys Val Ser Phe

145 150 155 160

Cys Tyr Met His His Met Glu Leu Pro Thr Gly Val His Ala Gly Thr

165 170 175

Asp Leu Glu Gly Asn Phe Tyr Gly Pro Phe Val Asp Arg Gln Thr Ala

180 185 190

Gln Ala Ala Gly Thr Asp Thr Thr Ile Thr Val Asn Val Leu Ala Trp

195 200 205

Leu Tyr Ala Ala Val Ile Asn Gly Asp Arg Trp Phe Leu Asn Arg Phe

210 215 220

Thr Thr Thr Leu Asn Asp Phe Asn Leu Val Ala Met Lys Tyr Asn Tyr

225 230 235 240

Glu Pro Leu Thr Gln Asp His Val Asp Ile Leu Gly Pro Leu Ser Ala

245 250 255

Gln Thr Gly Ile Ala Val Leu Asp Met Cys Ala Ser Leu Lys Glu Leu

260 265 270

Leu Gln Asn Gly Met Asn Gly Arg Thr Ile Leu Gly Ser Ala Leu Leu

275 280 285

Glu Asp Glu Phe Thr Pro Phe Asp Val Val Arg Gln Cys Ser Gly Val

290 295 300

Thr Phe Gln Leu Glu His His His His His His

305 310 315