CN111220429A - Array high-flux protein sample pretreatment device - Google Patents
Array high-flux protein sample pretreatment device Download PDFInfo
- Publication number
- CN111220429A CN111220429A CN201811406709.6A CN201811406709A CN111220429A CN 111220429 A CN111220429 A CN 111220429A CN 201811406709 A CN201811406709 A CN 201811406709A CN 111220429 A CN111220429 A CN 111220429A
- Authority
- CN
- China
- Prior art keywords
- temperature
- sample
- denaturation
- heating
- pump
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/44—Sample treatment involving radiation, e.g. heat
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/62—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating the ionisation of gases, e.g. aerosols; by investigating electric discharges, e.g. emission of cathode
- G01N27/622—Ion mobility spectrometry
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Abstract
The invention relates to an array high-flux protein sample pretreatment device, which is a sample treatment system capable of simultaneously carrying out online denaturation, reduction, desalination and enzymolysis on a plurality of protein samples, and comprises: the system comprises a protein processing module, a power supply module, a heating control module, a pump and a pump control module. The present invention features that on the basis of single protein pre-treating instrument, eight simultaneous treatments are added, each operation module of the single device is re-optimized in circuit, control and liquid flow path, and the modules are integrated into one operation device in optimal mode to control eight simultaneous treatments. The device is simple to operate, accurate and reliable in control, large in sample handling capacity and capable of meeting the detection requirements of large-batch samples.
Description
Technical Field
The invention relates to a high-flux protein sample pretreatment device, which is a sample treatment system capable of simultaneously carrying out online denaturation, reduction, desalination and enzymolysis on a plurality of protein samples.
Background
With the development of protein separation and detection technology, some special parameters and indexes increasingly attract attention in the medical field, and thus, the demand for large-batch and rapid clinical sample detection is generated.
The traditional proteome sample pretreatment comprises the steps of denaturation, reduction, alkylation, desalination, enzymolysis and the like, is usually carried out off-line manually, not only takes long time, but also has the possibility of sample pollution and loss, and seriously influences the result of large-scale protein analysis. Therefore, the development of an on-line protein sample pretreatment method and device has very important significance. However, the existing on-line proteome sample processing system can only integrate a few steps (such as on-line enzymolysis, analytical Chimica acta,2018,1000, 172-179; Talanta,2015,141,235-238.) or can only process one sample at a time, and is difficult to meet the requirement of the field of clinic and the like for large-array sample analysis, so in order to solve the above problems, an array type on-line proteome sample processing system (patent number: 201210517241.4) is further developed on the basis of a high-throughput proteome sample pre-processing device developed in the previous period
The device is protein sample pretreatment equipment with online protein denaturation, reduction, desalting and online enzymolysis functions. The device can realize high-flux and low-loss pretreatment of protein samples, and has good application prospect in proteomics research and clinical examination.
Disclosure of Invention
The invention aims to provide a sample pretreatment device integrating protein denaturation, reduction, desalting and online enzymolysis, and the realization of the function needs to control the transportation of exchange liquid, control high-temperature denaturation and reduction and enzyme reaction at a certain temperature, so the invention adopts the following technical scheme.
An array high-throughput protein sample pretreatment device, comprising: the system comprises a protein pretreatment module, a power supply module, a heating control module, a pump and a pump control module. The method specifically comprises the following steps: a high temperature denaturation and reduction unit component, a solvent displacer component, an enzyme reactor component, a heater power supply, a pump driving power supply, a heating controller, a pump flow controller and an infusion pump.
The high-temperature denaturation and reduction device assembly and the exchange liquid in the solvent displacer assembly are respectively completed by the infusion pump in a serial conveying mode, and the flowing mode can ensure that the flow rate of each assembly of the high-temperature denaturation and reduction device is the same.
The power module is respectively a high-temperature denaturation and reduction device component and an enzyme reactor component heating power supply and a pump power supply, and the high-temperature denaturation and reduction device component and the enzyme reactor component adopt a parallel heating mode respectively to ensure that the temperature of each heating element is the same.
The heating controller provides temperature control for the high-temperature denaturation and reduction component and the enzyme reactor component respectively.
The infusion pump is respectively a high-temperature denaturation and reduction device component, a solvent displacer component and an infusion liquid.
And the pump flow controllers respectively provide flow control for the infusion pumps.
The liquid-exchanging pump uses 4 pumps to divide into 2 groups, which are high-temperature denaturation and reduction components, and the solvent displacer component is used for conveying the exchanging liquid, so that the fluid pressure and the flow rate can be ensured to be stable, and the liquid-exchanging pump adopts the liquid-exchanging mode of connecting flow paths in series.
The high-temperature denaturation and reduction device assembly and the solvent displacer assembly are heated by adopting parallel circuits, so that the heating parts have stable and uniform heat, and the safety voltage of 36V is respectively used to ensure the safety of the electricity environment of the instrument.
The heating controller adopts sensor device parallel connection, can switch the temperature of observing every heating device, avoids every detected parts to detect respectively and control and causes instrument cost to increase, and the volume increases, the scheduling problem to can guarantee that every heating part temperature is unanimous.
The array high-throughput protein pretreatment equipment can be applied to proteome sample treatment of clinical, food safety, environmental exposure crowd and the like.
The invention has the following characteristics:
1, each operation unit module of the whole instrument is optimized, and the modules are optimally matched.
2, the sample processing capacity is large, the power consumption is low, and the method is safe and reliable.
3, the operation and the component replacement are convenient, and the maintenance is simple.
Drawings
FIG. 1 is a diagram of the array device processing of real samples, wherein (a), (b) and (c) are the results of the array device processing Hela samples in three ways;
FIG. 2 is a graph of the array device processing of real samples, wherein six lanes of the array device (a) (b) (c) (d) (e) (f) process plasma sample results separately;
FIG. 3 is a schematic diagram of an array high-throughput protein sample pretreatment apparatus.
Detailed Description
The experiment adopts eight high-throughput protein sample pretreatment devices, eight high-temperature denaturation and reduction devices, eight solvent displacers, eight enzyme reactors and eight samples for simultaneous operation, four pumps are used for dividing the samples into two groups, and exchange liquid is respectively conveyed to the high-temperature denaturation and reduction devices and the solvent displacers,
example 1
As shown in FIG. 1, the pump driving power source (04) was turned on in the connected system, and all of the high temperature denaturing and reducing device modules (06) were filled with a mixed solution of 2M guanidine hydrochloride and 10mM DTT, all of the solvent displacer modules (07) were filled with a 50mM ammonium bicarbonate solution, and a 6cm long enzyme column was connected as an enzyme reactor module (08). Meanwhile, a heater power supply (05) is turned on, and the temperature of the heating controller (03) is set to be 95 ℃.
3 aliquots of 4. mu.L of 8M urea-extracted Hela cellular protein (BCA assay concentration of 3mg/mL) were each diluted ten-fold with 50mM ammonium bicarbonate solution. After the temperature of the component (06) reaches 95 ℃, simultaneously introducing Hela cell protein samples into different pipelines of the whole system at a speed of 1 mu L/min by means of an injector respectively. After the end of the introduction, 20. mu.L of a 50mM ammonium hydrogencarbonate solution was introduced into the system. The solvent displacer component (07) is ensured to be operated all the time in the system operation. Meanwhile, each part was collected to obtain an enzymatic substance, which was 25. mu.L. Formic acid was added to the collected samples to ensure a final mass fraction of 0.1% formic acid in the solution. The latter groups were centrifuged at 16000rpm for 20 min. Each group was analyzed by Q-Exactive mass spectrometry and 5. mu.L each was loaded. The number of the identified proteins is 2100, 2008 and 2156 respectively.
Example 2
The pump driving power supply (04) was turned on in the connected system, and all the high temperature denaturing and reducing device modules (06) were filled with a mixed solution of 6M guanidine hydrochloride and 50mM DTT, all the solvent displacer modules (07) were filled with a 50mM ammonium bicarbonate solution, and a 4cm long enzyme column was connected as the enzyme reactor module (08). Meanwhile, a heater power supply (05) is turned on, and the temperature of the heating controller (03) is set to be 95 ℃.
6 portions of human normal plasma samples diluted to a concentration of 0.1mg/mL with 1 XPBS were taken at 100. mu.L. After the temperature of the component (06) reaches 95 ℃, the plasma samples are simultaneously introduced into different pipelines of the whole system at the speed of 8 mu L/min by means of syringes respectively. After the end of the introduction, 100. mu.L of a 50mM ammonium hydrogencarbonate solution was introduced into the system. The solvent displacer component (07) is ensured to be operated all the time in the system operation. Meanwhile, each part was collected to obtain an enzymatic substance, which was 70. mu.L. After freeze-drying the samples, each group was reconstituted with 8 μ L of 0.1% FA. The latter groups were centrifuged at 16000g for 20 min. Each group was subjected to Q-active mass spectrometry, and 3. mu.L each was loaded. The number of the identified proteins is 220, 218, 225, 206, 236 and 210 respectively.
Claims (7)
1. An array high-throughput protein sample pretreatment device, comprising: more than 2 high-temperature denaturation and reduction devices (06), more than 2 solvent replacers (07), more than 2 enzyme reactors (08), a heater power supply (05), a pump driving power supply (04), a heating controller (03), a pump flow controller (02) and an infusion pump (01);
the method is characterized in that:
the high-temperature denaturation and reduction device (06) is a hollow closed chamber, an exchange solution inlet and an exchange solution outlet are arranged on the chamber, a hollow fiber membrane is arranged in the chamber, and two ends of the hollow fiber membrane penetrate through the side wall of the chamber and are respectively connected with the sample inlet and the sample outlet; the solvent displacer (07) is a hollow closed cavity, an exchange fluid inlet and an exchange fluid outlet are arranged on the cavity, a hollow fiber membrane is arranged in the cavity, and two ends of the hollow fiber membrane penetrate through the side wall of the cavity and are respectively connected with the sample inlet and the sample outlet;
a sample outlet of the high-temperature denaturation and reduction device is connected with a sample inlet of the solvent displacer, the sample outlet of the solvent displacer is connected with a sample inlet of the enzyme reactor (08), and reaction liquid in the enzyme reactor (08) is discharged from the sample outlet to form a continuous protein sample pretreatment structure;
among more than 2 protein sample pretreatment structures: the exchange liquid in more than 2 high-temperature denaturation and reduction devices is connected with a denaturation and reduction exchange liquid storage tank by an infusion pump in a mode of sequential serial delivery; the flowing mode can ensure that the flow of each component of the high-temperature denaturation reducer is the same; the exchange liquid in more than 2 solvent displacers is connected with an exchange liquid storage tank for displacing the solvent by an infusion pump in a mode of sequential serial delivery;
an electric heating element and a temperature sensor are respectively arranged on the high-temperature denaturation and reduction device (06) and the enzyme reactor (08);
the power module includes: a heating power supply (05) and a pump driving power supply (04) which are electric heating elements of a high-temperature denaturation and reduction device (06) and an enzyme reactor (08), wherein the electric heating elements of the high-temperature denaturation and reduction device assembly (06) and the enzyme reactor assembly (08) respectively adopt a parallel heating mode; ensuring that the temperature of each heating element is the same;
the heating controller (03) is used for respectively providing temperature control for the high-temperature denaturation and reduction device assembly (06) and the enzyme reactor assembly (08);
the infusion pump (01) is divided into more than two groups, namely a high-temperature denaturation and reduction device assembly (06) and a solvent displacer assembly (07) which are used for conveying exchange liquid;
and the pump flow controllers (02) respectively provide flow control for the infusion pumps (01).
2. The arrayed high throughput protein pretreatment apparatus according to claim 1, wherein:
the transfer pump (01) of the exchange liquid is divided into 2 groups for 4 pumps, 2 groups are respectively a high-temperature denaturation and reduction device assembly (06), the solvent displacer assembly (07) transfers the exchange liquid, the stability of the fluid pressure and the flow rate can be ensured, and the transfer mode of connecting flow paths in series is adopted.
3. An arrayed high throughput protein pretreatment apparatus according to claim 1, wherein: the high-temperature denaturation and reduction device assembly (06) and the solvent displacer assembly (07) are heated by adopting parallel circuits, so that the heating parts are stable and uniform in heat, and the safety of the electricity environment of the instrument is ensured by respectively using 36V safety voltage.
4. An arrayed high throughput protein pretreatment apparatus according to claim 1, wherein:
the heating controller (03) adopts the parallel connection of the sensing devices, can switch and observe the temperature of each heating device, avoids the problems of instrument cost increase, volume increase and the like caused by the fact that each detected part is respectively detected and controlled, and can ensure the temperature of each heating part to be consistent.
5. The arrayed high-throughput protein pretreatment apparatus according to claim 1 or 4, wherein: the heating controller (03) is a temperature controller and respectively provides temperature control for the high-temperature denaturation and reduction device component (06) and the enzyme reactor component (08); the temperature sensor is in signal connection with the temperature controller, and the electric heating element is connected with the heating power supply (05) through the temperature controller.
6. An arrayed high throughput protein pretreatment apparatus according to claim 1, wherein: the pump flow controller (02) is a pump flow control board.
7. The array high-throughput protein pretreatment apparatus of claim 1, being applicable to proteome sample processing in clinical, food safety or environmental exposure populations.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811406709.6A CN111220429A (en) | 2018-11-23 | 2018-11-23 | Array high-flux protein sample pretreatment device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811406709.6A CN111220429A (en) | 2018-11-23 | 2018-11-23 | Array high-flux protein sample pretreatment device |
Publications (1)
Publication Number | Publication Date |
---|---|
CN111220429A true CN111220429A (en) | 2020-06-02 |
Family
ID=70826995
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811406709.6A Pending CN111220429A (en) | 2018-11-23 | 2018-11-23 | Array high-flux protein sample pretreatment device |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111220429A (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1263893A (en) * | 1999-02-05 | 2000-08-23 | 上海复旦张江生物医药有限公司 | Renaturation equipment of modified protein |
CN1331345A (en) * | 2000-07-04 | 2002-01-16 | 清华大学 | Integrated microarray device |
CN1995319A (en) * | 2007-01-12 | 2007-07-11 | 北京工业大学 | Multiple passage intelligent temperature-control device facing PCR microfluidic chip |
CN101838609A (en) * | 2010-03-15 | 2010-09-22 | 上海浩源生物科技有限公司 | Sample adding device and application thereof |
CN102206573A (en) * | 2011-03-22 | 2011-10-05 | 博奥生物有限公司 | Automatic sample introduction device for microarray chip and automatic sample introduction hybridization microarray chip |
CN103852527A (en) * | 2012-12-05 | 2014-06-11 | 中国科学院大连化学物理研究所 | High-flux protein sample pre-treatment device |
CN106255542A (en) * | 2014-02-17 | 2016-12-21 | 拜耳公司 | For from buffering or the ultra filtration unit of Medium Exchange continuously of protein solution |
CN107588997A (en) * | 2016-07-08 | 2018-01-16 | 中国科学院大连化学物理研究所 | A kind of high throughput protein sample pretreatment equipment |
-
2018
- 2018-11-23 CN CN201811406709.6A patent/CN111220429A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1263893A (en) * | 1999-02-05 | 2000-08-23 | 上海复旦张江生物医药有限公司 | Renaturation equipment of modified protein |
CN1331345A (en) * | 2000-07-04 | 2002-01-16 | 清华大学 | Integrated microarray device |
CN1995319A (en) * | 2007-01-12 | 2007-07-11 | 北京工业大学 | Multiple passage intelligent temperature-control device facing PCR microfluidic chip |
CN101838609A (en) * | 2010-03-15 | 2010-09-22 | 上海浩源生物科技有限公司 | Sample adding device and application thereof |
CN102206573A (en) * | 2011-03-22 | 2011-10-05 | 博奥生物有限公司 | Automatic sample introduction device for microarray chip and automatic sample introduction hybridization microarray chip |
CN103852527A (en) * | 2012-12-05 | 2014-06-11 | 中国科学院大连化学物理研究所 | High-flux protein sample pre-treatment device |
CN106255542A (en) * | 2014-02-17 | 2016-12-21 | 拜耳公司 | For from buffering or the ultra filtration unit of Medium Exchange continuously of protein solution |
CN107588997A (en) * | 2016-07-08 | 2018-01-16 | 中国科学院大连化学物理研究所 | A kind of high throughput protein sample pretreatment equipment |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101250483B (en) | Combined splint microelectrode type micro-fluidic dielectrophoresis cell separation and enrichment chip | |
CN103103106B (en) | Device for automatically analyzing nucleic acid | |
CN104487835B (en) | Pre-processing electrophoresis integral flask, the one-piece type capillary electrophoresis of pre-treatment and the one-piece type capillary electrophoresis method of pre-treatment | |
US11826760B2 (en) | Self-contained slide processing unit for biological specimens | |
US20090035746A1 (en) | Device and Method for Preparing a Sample for an Analysis and Device and Method for Analyzing a Sample | |
CN105349401A (en) | Multifunctional integrated microfluidic nucleic acid analysis chip and preparation and analysis method thereof | |
JP2006504957A (en) | Microfluidic system for analyzing nucleic acids | |
CN101039750A (en) | Method for carrying out an electrochemical measurement on a liquid measuring sample in a measuring chamber that can be accessed by lines, and corresponding arrangement | |
CA3126575C (en) | A system and method of performing a biological experiment with adaptive cybernetic control of procedural conditions | |
CN102269732A (en) | High speed electrolyte analysis apparatus | |
CN113604344B (en) | High-flux integrated micro-droplet digital PCR (polymerase chain reaction) realization system | |
Cantoni et al. | A microfluidic chip carrier including temperature control and perfusion system for long-term cell imaging | |
WO2018090652A1 (en) | High-throughput body fluid protein sample pretreatment apparatus and application thereof | |
CN111220429A (en) | Array high-flux protein sample pretreatment device | |
CN101718698A (en) | Laser-induced fluorescence analyzer with PCR-CE coupled microfluidic chip | |
CN103852527B (en) | High-flux protein sample pre-treatment device | |
CN107406816B (en) | Microbioprocessing system and method for producing proteins from human blood | |
EP3794103A2 (en) | Methods to incorporate machine learning analytics for optimizing protein purity, potency and quality in an on-demand production system for point-of-care delivery | |
CN114518240A (en) | Online sample analysis device | |
CN113302487B (en) | Electrophoresis apparatus capable of independently performing electrophoresis on multiple samples | |
CN108414609B (en) | Online mass spectrum detection device for nutrient component change process in traditional Chinese medicine steaming process | |
Giannitsis et al. | Usage of microfluidic lab-on-chips in biomedicine | |
CN214097497U (en) | Sample processing and detecting system | |
CN107588997A (en) | A kind of high throughput protein sample pretreatment equipment | |
KR20140028431A (en) | Pcr chip for detecting electrochemcial signal comprising heating block of repetitively disposed heater unit, real-time pcr device comprising the same, and real-time pcr using the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20200602 |