CN104693278A - Jagged1 agonist polypeptide and application thereof - Google Patents

Abstract

The invention discloses Jagged1 agonist polypeptide and application thereof, and relates to the field of medicines, in particular to polypeptide which can promote combination of Jagged1 and Notch and treats malignant tumor. The sequence is GDDCGTGGTCAAAALLPCVD and is a novel sequence, the Jagged1 agonist polypeptide can suppress proliferation of melanoma cells and liver cancer stem cells outside the human body, and the survival rate of tumor-bearing mice is improved in the intra-body experiment. The Jagged1 agonist polypeptide can serve as a detection kit, and has potential novel medicine development value.

Description

A kind of Jaggedl agonist polypeptide and application thereof

Technical field

The present invention relates to Jaggedl agonist polypeptide and application thereof, be specifically related to that there is the combination promoting Jaggedl and Notch, the polypeptide for the treatment of malignant tumour.

Background technology

Tumor stem cell is the cell having self-renewal capacity in tumour and can produce heterogeneous cell.Tumor stem cell is to survival, propagation, the transfer of tumour and recur important role.In essence, tumor stem cell maintains the vitality of tumor cell group by self and unlimited increment; Motion and the ability of migrating of tumor stem cell make again the transfer of tumour cell become possibility; Tumor stem cell can be in dormant state for a long time and have several drug resistance molecule and insensitive to the extraneous chemical factors of killing tumor cell, therefore tumour often for some time recurrence after conventional tumor therapeuticing method eliminates most of Common tumors cell.

Research finds, in tumor stem cell, Notch signal representation is higher than normal cell, although also have activated tumor stem cell after suppressing Notch activity, but can not form tumour. and under the tumour of control group, cell can form tumour, and after suppressing Notch activity under tumour cell quantity obviously reduce.So Notch signal forms in neoplastic process the ability that can reduce tumor stem cell and change to malignant tumour at tumor stem cell.

Jaggedl is the part of Notch signal transduction pathway in Mammals, after the Notch combination of Jaggedl and flanking cell, Notch is cut by proteasome, discharge the cytoplasmic region ICN (intracellular domain of Notch) with nuclear localization signal, enter nucleus and CLS (a class DBP) combines, regulatory gene is expressed.Improve the binding affinity of Jaggedl and Notch, promote the combination of Jaggedl and Notch, effectively can reduce the activity of tumor stem cell, the growth of Tumor suppression, thus reach the effect for the treatment of tumour.

At present, do not have the Jaggedl agonist polypeptide of ripe exploitation to come out, be used for the treatment of malignant tumour.

Jaggedl agonist polypeptide in this patent has proved in melanomatosis effective, has the prospect developed in other tumor models.

Summary of the invention

Goal of the invention

The invention provides brand-new sequence, this sequence is Jaggedl agonist, has good curative effect to malignant tumour.

Technical scheme

Jaggedl agonist polypeptide, is characterized in that its sequence is GDDCGTGGTCAAAALLPCVD.

The application of described Jaggedl agonist polypeptide in preparation tumor.

The application of described Jaggedl agonist polypeptide in preparation treatment melanoma medicine.

Described Jaggedl agonist polypeptide is preparing the application in Hepatoma therapy medicine.

Detect a test kit for tumour, it contains Jaggedl agonist polypeptide according to claim 1.Described test kit, is characterized in that also having

(1) the 0.05mol/L carbonate buffer solution of coating buffer: pH9.6;

(2) the 0.02mol/L phosphate buffered saline buffer of PBS damping fluid: pH7.4;

(3) 0.02mol/LPBS and 0.2%BSA of antibody diluent: pH7.4;

(4) the 0.05mol/L carbonate buffer solution of confining liquid: pH9.6 and 2.0%BSA

(5) washings: 0.02mol/LPBS (pH7.4) and 0.05%Tween-20;

(6) substrate solution: solubility single-component tmb substrate solution;

(7) stop buffer: 2mol/L sulphuric acid soln;

(8) Notch antibody;

(9) goat anti-mouse IgG.

Beneficial effect

Utilize solid-phase synthesis chemosynthesis Jaggedl agonist polypeptide, this polypeptide has brand-new sequence, this polypeptide can external promotion Jaggedl and Notch combination, treat malignant tumour, as melanoma.The Jaggedl agonist polypeptide that we find can simultaneously check melanin tumor cell proliferation vigor, and improves tumor-bearing mice survival rate in test in vivo, has potential new drug development value.

Embodiment

Jaggedl agonist polypeptide is synthesized by the raw work in Shanghai.

Embodiment 1

Jaggedl agonist polypeptide is to the growth of vitro culture human melanoma cell and survival IC50.

Adopt MTT colorimetry.By the human melanoma cell of logarithmic growth, add in 96 well culture plates with 1.0 × 105, cultivate 24h, experimental port, positive drug control hole add Experimental agents Jaggedl agonist polypeptide (the raw work synthesis in Shanghai) and the positive control medicine taxol of different concns respectively; Blank group adds the solvent of same volume.Five multiple holes are established in every hole, cultivate 48h, respectively 0h, 2h, 8h, 14h, 20h, 24h, 36h, the every hole of 48h adds MTT, after effect 4h, add DMSO, hatch 30min, absorbance A value is measured, by formula human melanoma cell growth inhibition ratio=(1-experimental group light absorption value/control group light absorption value) × 100% at microplate reader 620nm place.The IC50 calculating Experimental agents is 5.57 μMs, 4.43 μMs of positive control drug, illustrates that Jaggedl agonist polypeptide has significant Tumor suppression active.

Embodiment 2

Jaggedl agonist polypeptide is to the growth of vitro culture of human liver-cancer stem cell and survival IC50.

Adopt MTT colorimetry.By people's liver-cancer stem cell of logarithmic growth, add in 96 well culture plates with 1.0 × 105, cultivate 24h, experimental port, positive drug control hole add Experimental agents Jaggedl agonist polypeptide (the raw work synthesis in Shanghai) and the positive control medicine taxol of different concns respectively; Blank group adds the solvent of same volume.Five multiple holes are established in every hole, cultivate 48h, respectively 0h, 2h, 8h, 14h, 20h, 24h, 36h, the every hole of 48h adds MTT, after effect 4h, add DMSO, hatch 30min, absorbance A value is measured, by formula people liver-cancer stem cell growth inhibition ratio=(1-experimental group light absorption value/control group light absorption value) × 100% at microplate reader 620nm place.The IC50 calculating Experimental agents is 10.54 μMs; 6.51 μMs of positive control drug, illustrate that Jaggedl agonist polypeptide has significant Tumor suppression active.

Embodiment 3

With vigor in the body of tumor model detection Jaggedl agonist polypeptide.

Set up melanoma tumor model, positive control medicine taxol 10mg/Kg; 5,10,20mg/Kg blank group adds the solvent of same volume, and experimental group polypeptide establishes 3 dosage:.After 21 days, observe mouse survival quantity, calculate survival rate.Result shows, and Jaggedl agonist polypeptide can protect small white mouse effectively, improves the survival rate of tumor-bearing mice, 5,10,20mg/Kg, and positive group survival rate reaches and is followed successively by 99%, 91.1%, 85% and 56%.Illustrate that Jaggedl agonist polypeptide has good security.

The ELISA kit of embodiment 4 containing Jaggedl agonist polypeptide detects

Enzyme connects immunoadsorption assay (ELISA) test kit and comprises following reagent:

(1) coating buffer: 0.05mol/L carbonate buffer solution (pH9.6).Take 0.75g sodium carbonate, 1.46g sodium bicarbonate, add deionized water and be settled to 500ml;

(2) PBS damping fluid: 0.02mol/L phosphate buffered saline buffer (pH7.4).Take 0.2g potassium primary phosphate, 2.90g Sodium phosphate dibasic, 8g sodium-chlor, add deionized water constant volume to 1000ml;

(3) antibody diluent: 0.02mol/LPBS (pH7.4) and 0.2%BSA.Take 0.2gBSA to add the 0.02mol/L phosphate buffered saline buffer for preparing and dissolve quantitatively to 100ml;

(4) confining liquid: 0.05mol/L carbonate buffer solution (pH9.6) and 2.0%BSA.2.0gBSA adds the 0.05mol/L carbonate buffer solution prepared and dissolves quantitatively to 100ml;

(5) washings: 0.02mol/LPBS (pH7.4) and 0.05%Tween-20.50ulTween-20 is dissolved in 100ml0.02mol/L phosphate buffered saline buffer, concussion mixing;

(6) substrate solution: solubility single-component tmb substrate solution;

(7) stop buffer: 2mol/L sulphuric acid soln.The 10ml98% vitriol oil adds in 60ml distilled water, is settled to 100ml, room temperature preservation;

(8) Jaggedl agonist polypeptide

(9) Notch antibody (primary antibodie) is synthesized by the raw work in Shanghai.

(10) two anti-(goat anti-mouse IgG) are purchased from the prompt Science and Technology Ltd. of Amy

Using method:

1, serum sample preparation: get 3 tumor bearing nude mices, carry out eye socket and get blood, every only 200 μ L, Quick spin 12000rpm 3min, get supernatant, 1:2 adds PBS by volume, 80 DEG C of water-bath 30min, and 12000rpm3min gets supernatant, and-20 DEG C frozen for subsequent use.。

2, Notch antibody is coated antibody, and Notch antibody is dissolved in bag by diluent, concentration is 100 μ g/mL.The 96 every holes of hole enzyme plate add 100 μ L, and 4 DEG C of bags are spent the night.Discard coating buffer, add confining liquid 200 μ L, 37 DEG C of closed 1h.Discard confining liquid, add serum sample 100 μ L (thinning ratio 1:50) of sample diluting liquid dilution and the mixture of Jaggedl agonist polypeptide 100 μ L (10 μ g/ml) and above-mentioned serum sample 50 μ L and Jaggedl agonist polypeptide 50 μ L respectively, be divided into 3 groups, hatch 1h for 37 DEG C.Discard serum, PBST and tap water interval wash three times.After washing, every hole adds sample diluting liquid dilution ELIAS secondary antibody 100 μ L (thinning ratio 1:10000), hatches 1h for 37 DEG C.Discard two to resist, washing.After washing, every hole adds 100 μ L substrate solutions (50 μ L substrate A, 50 μ L substrate B), after 37 DEG C of reaction 30min, adds 50 μ L 2M H ₂sO ₄termination reaction, measures the optical density value OD in every hole at 450nm wavelength by microplate reader _450nm.Result: Jaggedl agonist polypeptide can with Notch antibodies, and Notch albumen in serum can be competed, therefore illustrate that Jaggedl agonist polypeptide competition law detects Notch, realize tumour prediction;

SEQUENCE LISTING

 

Pu Luoda bio tech ltd, <110> Suzhou

 

<120> Jaggedl agonist polypeptide and application thereof

 

<130>

 

<160> 1

 

<170> PatentIn version 3.3

 

<210> 1

<211> 20

<212> PRT

<213> artificial sequence

 

<400> 1

 

Gly Asp Asp Cys Gly Thr Gly Gly Thr Cys Ala Ala Ala Ala Leu Leu

1 5 10 15

 

 

Pro Cys Val Asp

20

Claims (6)

1.Jaggedl agonist polypeptide, is characterized in that its sequence is GDDCGTGGTCAAAALLPCVD.

2. the application of Jaggedl agonist polypeptide as claimed in claim 1 in preparation tumor.

3. the application of Jaggedl agonist polypeptide as claimed in claim 1 in preparation treatment melanoma medicine.

4. Jaggedl agonist polypeptide as claimed in claim 1 is preparing the application in Hepatoma therapy medicine.

5. detect a test kit for tumour, it contains Jaggedl agonist polypeptide according to claim 1.

6. test kit as claimed in claim 5, is characterized in that also having

(1) the 0.05mol/L carbonate buffer solution of coating buffer: pH9.6;

(2) the 0.02mol/L phosphate buffered saline buffer of PBS damping fluid: pH7.4;

(3) 0.02mol/LPBS and 0.2%BSA of antibody diluent: pH7.4;

(4) the 0.05mol/L carbonate buffer solution of confining liquid: pH9.6 and 2.0%BSA

(5) washings: 0.02mol/LPBS (pH7.4) and 0.05%Tween-20;

(6) substrate solution: solubility single-component tmb substrate solution;

(7) stop buffer: 2mol/L sulphuric acid soln;

(8) Notch antibody;

(9) goat anti-mouse IgG.