Quantitative method for dimensional electrophoresis protein sample

A two-dimensional electrophoresis, protein technology, applied in the biological field, can solve the problems of affecting the quantitative accuracy, many operation steps, can not be used, etc., to achieve the effect of good linearity and repeatability

Inactive Publication Date: 2014-09-03
ZUNYI MEDICAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Reagents such as urea, thiourea, Triton X-100 (Triton X-100), sodium dodecyl sulfate (SDS) and other reagents used in this process are easy to react with BCA and Coomassie brilliant blue (CBB) to develop color, thereby Affects absorbance values ​​and thus quantification accuracy, so neither method can be used for 2-D expe

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] A quantitative method for protein that can be used in two-dimensional electrophoresis technology, taking the two-dimensional electrophoresis protein sample of human gastric adenocarcinoma SGC-7901 cells as an example, comprising the following steps:

[0020] (1) Two-dimensional electrophoresis protein sample preparation: Take 10 mg of human gastric adenocarcinoma SGC-7901 cell sample, add 1 mL two-dimensional electrophoresis cell lysate (7mol / L urea, 2mol / L thiourea, 4% 3-[(3- Choleamidopropyl) dimethylammonium] -1-propanesulfonate, 65mmol / L dithiothreitol), resuspended and collected in a 15mL centrifuge tube for sonication on ice, 10s for each sonication, 10s pause, A total of 5 cycles; centrifuge at 4°C and 14000g for 30min, transfer the supernatant to a new centrifuge tube, store at -80°C after aliquoting;

[0021] (2) Preparation of mixed solutions of standard protein and Coomassie Brilliant Blue G-250 at different concentrations (for drawing a standard curve): prep...

Embodiment 2

[0029] A quantitative method for a protein that can be used in two-dimensional electrophoresis technology, taking a human liver cancer HepG2 cell two-dimensional electrophoresis protein sample as an example, includes the following steps:

[0030] (1) Two-dimensional electrophoresis protein sample preparation: take 100 mg of human liver cancer HepG2 cell sample, add 5 mL two-dimensional electrophoresis cell lysate (9mol / L urea, 4% mass concentration of 3-[(3-cholamidopropyl) dimethyl Ammonium]-1-propanesulfonate, 65mmol / L dithiothreitol), resuspended and collected in a 15mL centrifuge tube for sonication on ice, each sonication for 10s, pause for 10s, a total of 5 cycles; 4°C, 14000g Centrifuge for 30 minutes, transfer the supernatant to a new centrifuge tube, store at -80°C after aliquoting;

[0031] (2) Preparation of mixed solutions of standard protein and Coomassie Brilliant Blue G-250 at different concentrations (for drawing a standard curve): prepare 1 mg / mL bovine serum ...

Embodiment 3

[0039] A quantitative method for protein that can be used in two-dimensional electrophoresis technology, taking the two-dimensional electrophoresis protein sample of human cervical cancer Hela cells as an example, comprising the following steps:

[0040] (1) Two-dimensional electrophoresis protein sample preparation: Take 50 mg of human cervical cancer Hela cell sample, add 3 mL two-dimensional electrophoresis cell lysate (7mol / L urea, 2mol / L thiourea, 3-[(3-cholesterol with a mass concentration of 4%) Aminopropyl) dimethylammonium] -1-propanesulfonate, 65mmol / L dithiothreitol), resuspended and collected in a 15mL centrifuge tube for sonication on ice, 10s for each sonication, 10s pause, total 5 cycles, centrifuge at 4°C, 14000g for 30min, transfer the supernatant to a new centrifuge tube, store at -80°C after aliquoting;

[0041] (2) Preparation of mixed solutions of standard protein and Coomassie Brilliant Blue R-250 at different concentrations (for drawing a standard curve)...

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PUM

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Abstract

The invention discloses a quantitative method for a dimensional electrophoresis protein sample. The method includes the steps of: preparing a dimensional electrophoresis sample; preparing a 1-2mg / mL bovine serum albumin (BSA) solution by using the a dimensional electrophoresis cell lysate, taking 8 centrifuge tubes, adding 0-200 muL of bovine serum albumin solution respectively, and supplementing ultrapure water to 1 mL to reach a final concentration of standard protein of 0-0.2mg /ml, then adding 5 mL of a 0.01% Coomassie brilliant blue G-250 or R-250 dye solution into each centrifuge tube, and fully mixing to obtain standard mixture solutions with different concentrations; preparing a dimensional electrophoresis sample mixed solution; adding the sample decrypting and framing fluorescence intensity; drawing a standard curve; and calculating the concentration of the dimensional electrophoresis protein sample. The invention has the advantages of simple operation, accuracy, fastness and cheapness.

Description

technical field [0001] The invention belongs to the field of biotechnology, and relates to a protein quantification method. [0002] Background technique [0003] Protein quantification is an important link in cell and molecular biology experiments. Commonly used protein quantification methods include the biquinolinic acid method (BCA method) and the Coomassie brilliant blue method (Bradford method) invented by Bradford MM in 1976, both of which are quantitative methods based on absorbance values. Two-dimensional electrophoresis (2-D) is the core technology in the process of proteomics research. Due to the complex process of 2-D protein sample processing, a wide variety of reagents are used. Reagents such as urea, thiourea, Triton X-100 (Triton X-100), sodium dodecyl sulfate (SDS) and other reagents used in this process are easy to react with BCA and Coomassie brilliant blue (CBB) to develop color, thereby These two methods cannot be used in 2-D experiments because they a...

Claims

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Application Information

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IPC IPC(8): G01N21/64
Inventor 刘云曹嵩李晓飞朱欣婷胡姗姗卜雯雯邓文文刘仕福
Owner ZUNYI MEDICAL UNIVERSITY
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