CN107215860A - A kind of preparation method of the orderly self-assembled structures of graphene/DNA - Google Patents

A kind of preparation method of the orderly self-assembled structures of graphene/DNA Download PDF

Info

Publication number
CN107215860A
CN107215860A CN201610159601.6A CN201610159601A CN107215860A CN 107215860 A CN107215860 A CN 107215860A CN 201610159601 A CN201610159601 A CN 201610159601A CN 107215860 A CN107215860 A CN 107215860A
Authority
CN
China
Prior art keywords
graphene
dna
assembled structures
preparation
orderly self
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.)
Granted
Application number
CN201610159601.6A
Other languages
Chinese (zh)
Other versions
CN107215860B (en
Inventor
钱伟
赵胜民
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lv Qi (beijing) Biological Technology Co Ltd
Original Assignee
Lv Qi (beijing) Biological Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lv Qi (beijing) Biological Technology Co Ltd filed Critical Lv Qi (beijing) Biological Technology Co Ltd
Priority to CN201610159601.6A priority Critical patent/CN107215860B/en
Publication of CN107215860A publication Critical patent/CN107215860A/en
Application granted granted Critical
Publication of CN107215860B publication Critical patent/CN107215860B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Saccharide Compounds (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

A kind of preparation method of the orderly self-assembled structures of graphene/DNA, this method comprises the following steps:(1)Silicon chip polyglutamic acid or the polyacrylic acid solution immersion modification of graphene will be loaded with;(2)Soaked and modified with single stranded DNA solution, i.e., in the graphenic surface formation orderly self-assembled structures of DNA.The invention provides a kind of highly versatile, the orderly self-assembled structures of graphene/DNA of functionalization, to replace the conventional self-assembled structures in rigid substrate in the prior art, application of the orderly self-assembled structures of DNA in biochemistry detection, scientific research etc. numerous areas is effectively extended.

Description

A kind of preparation method of the orderly self-assembled structures of graphene/DNA
Technical field
The present invention relates to graphene composite material field, and in particular to a kind of orderly self-assembled structures of graphene/DNA and its Preparation method.
Background technology
There is graphene the carbon atom in Colloidal particles, plane to be connected to form hexagonal lattice with sp2 hybridized orbits Structure.Due to its unique physical property, graphene is considered as having huge in terms of sensitive electrical detection chemistry or biomolecule Prospect.
Before the sensitive detectors based on graphene are explored, first have to find it is practicable, can be to graphene table Face carries out the method for modifying of functionalization.Have been reported that(Mohanty, N.; Berry, V. Nano Lett. 2008, 8, 4469–4476.)The single stranded DNA that amido is ended up is by being covalently bound on graphene oxide.But what it was selected is not stone Black alkene, but graphene oxide, and its ordered fabrication for failing to realize surface DNA.In addition, having been reported that(Graphene-DNA hybrids: self-assembly and electrochemical detection performance)By DNA with graphite Alkene mixes to prepare graphene aqueous solution.It utilizes interaction strong between DNA and graphene, enables the DNA sides for being dissolved in water Graphene is helped to be dissolved in water.And ordered fabrication of the biomolecule such as DNA in graphenic surface how is realized, there is not report so far Road.
This area need develop it is a kind of can graphenic surface ordered fabrication biomolecule method, not only make graphene The integrality of lamella is not destroyed, can also be in graphenic surface ordered fabrication biomolecule.
The content of the invention
It is an object of the present invention to have by carrier of graphene there is provided graphene/DNA of a kind of highly versatile, functionalization Sequence self-assembled structures, to replace the conventional self-assembled structures in rigid substrate in the prior art, effectively extend DNA in order certainly Application of the package assembly in biochemistry detection, scientific research etc. numerous areas.
First, the invention provides a kind of preparation method of the orderly self-assembled structures of graphene/DNA, it is characterised in that should Method comprises the following steps:
(1)Silicon chip polyglutamic acid or the polyacrylic acid solution immersion certain time of graphene will be loaded with, then spent respectively Ionized water, absolute ethyl alcohol are cleaned, and are then dried up with nitrogen;
(2)Be dissolved with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides solvent be 0.01M-0.1M PBS The single stranded DNA solution immersion of buffer solution, is then cleaned with deionized water, absolute ethyl alcohol, is then dried up with nitrogen, i.e., in stone respectively Black alkene surface forms the orderly self-assembled structures of DNA.
Specifically, the silicon chip of graphene that is loaded with is peeled off graphene onto silicon chip using micromechanical forces stripping method.
To remove remained on surface, the silicon chip for being loaded with graphene is 1.0 × 10 in 350 DEG C of -600 DEG C of vacuums-6Pa- 1.0×10-4Vacuum annealing 2-5h is carried out under Pa, to remove the cull remained on silicon chip.
The concentration of 1- (3- the dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides used is 0.01M-0.1M.It is poly- Glutamic acid or polyacrylic acid solution weight average molecular weight are that 20000-50000, concentration are 0.1 mg/ml-2mg/ml.
It is 0.5h-2h to take into account soak time in efficiency and stability, step (1).Step(2)Middle soak time is 6h- 24h。
Specifically, the single-stranded DNA sequence is AAAAATTTTT.The specific DNA is certainly not limited to, in the prior art institute Be related to can in order self assembly DNA sequence dna can according to the present invention mentality of designing graphenic surface carry out self assembly.
The present invention has following technical advantage compared to prior art:
(1)The creative graphene that introduces as the substrate of DNA self assemblies, silicon different from the past, silica, mica, Quartz etc. hard material, graphene realizes the effect of flexible substrates with its unique single layer structure;
(2)The excellent physical property of graphene effectively can be attached to the orderly self assemblies of DNA using graphene as substrate In structure, so that the regulation and control to graphene physical property are realized, the influence of electron transport performance, its technology especially in graphene Effect and application prospect are beyond imagination.
(3)As a kind of general preparation method, the application is widely used, the DNA sequence dna of especially existing functionalization, It is fixed, ordering carries out scientific research, practical application to it wide significance and prospect.
Embodiment
Technical scheme is further explained below by embodiment, but protection scope of the present invention is not by reality Apply any formal limitation of example.
Embodiment 1
1. prepare graphene on silicon chip with mechanical stripping method, the silicon chip of graphene then will be loaded with 350 DEG C, and vacuum is 1.0×10-6Vacuum annealing 2h is carried out under Pa.
2. will be loaded with the silicon chip of graphene with weight average molecular weight is polyglutamic acidleach that 20000, concentration is 0.1mg/ml 2h is steeped, is then cleaned, is then dried up with nitrogen with deionized water, absolute ethyl alcohol respectively.
3. with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides are dissolved with, concentration is 0.04mg/ml's Solvent is the single stranded DNA solution immersion 8h of 0.01M PBS, is then cleaned respectively with deionized water, absolute ethyl alcohol, so Dried up afterwards with nitrogen.DNA used sequence is AAAAATTTTT in experiment, and 1- (3- dimethylamino-propyls) -3- ethyls carbon two is sub- The concentration of amine hydrochlorate is 0.01M.
Embodiment 2
1. prepare graphene on silicon chip with mechanical stripping method, the silicon chip of graphene then will be loaded with 450 DEG C, and vacuum is 1.0×10-4Vacuum annealing 5h is carried out under Pa.
2. will be loaded with the silicon chip of graphene with weight average molecular weight is polyglutamic acidleach that 40000, concentration is 0.5 mg/ml 1h is steeped, is then cleaned, is then dried up with nitrogen with deionized water, absolute ethyl alcohol respectively.
3. with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides are dissolved with, concentration is 0.08mg/ml's Solvent is the single stranded DNA solution immersion 6h of 0.05M PBS, is then cleaned respectively with deionized water, absolute ethyl alcohol, so Dried up afterwards with nitrogen.DNA used sequence is AAAAATTTTT in experiment, and 1- (3- dimethylamino-propyls) -3- ethyls carbon two is sub- The concentration of amine hydrochlorate is 0.04M.
Embodiment 3
1. prepare graphene on silicon chip with mechanical stripping method, the silicon chip of graphene then will be loaded with 500 DEG C, and vacuum is 1.0×10-6Vacuum annealing 2h is carried out under Pa.
2. will be loaded with the silicon chip of graphene with weight average molecular weight is polypropylene acidleach that 30000, concentration is 1.5 mg/ml 0.8h is steeped, is then cleaned, is then dried up with nitrogen with deionized water, absolute ethyl alcohol respectively.
3. with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides are dissolved with, concentration is 0.06mg/ml's Solvent is the single stranded DNA solution immersion of 0.04M PBS, is then cleaned respectively with deionized water, absolute ethyl alcohol, then Dried up with nitrogen.DNA used sequence is AAAAATTTTT, 1- (3- dimethylamino-propyls) -3- ethyl carbodiimides in experiment The concentration of hydrochloride is 0.05M.
Embodiment 4
1. prepare graphene on silicon chip with mechanical stripping method, the silicon chip of graphene then will be loaded with 600 DEG C, and vacuum is 1.0×10-5Vacuum annealing 3h is carried out under Pa.
2. will be loaded with the silicon chip of graphene with weight average molecular weight is polypropylene acidleach that 40000, concentration is 1.2 mg/ml 1.5h is steeped, is then cleaned, is then dried up with nitrogen with deionized water, absolute ethyl alcohol respectively.
3. with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides are dissolved with, concentration is 0.1mg/ml's Solvent is the single stranded DNA solution immersion of 0.1M PBS, is then cleaned respectively with deionized water, absolute ethyl alcohol, Ran Houyong Nitrogen is dried up.DNA used sequence is AAAAATTTTT, 1- (3- dimethylamino-propyls) -3- ethyl carbodiimide salt in experiment The concentration of hydrochlorate is 0.1M.
Embodiment 5
1. prepare graphene on silicon chip with mechanical stripping method, the silicon chip of graphene then will be loaded with 550 DEG C, and vacuum is 1.0×10-5Vacuum annealing 4h is carried out under Pa.
2. will be loaded with the silicon chip of graphene with weight average molecular weight is polypropylene acidleach that 30000, concentration is 1.5 mg/ml 2h is steeped, is then cleaned, is then dried up with nitrogen with deionized water, absolute ethyl alcohol respectively.
3. with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides are dissolved with, concentration is 0.2mg/ml's Solvent is the single stranded DNA solution immersion of 0.1M PBS, is then cleaned respectively with deionized water, absolute ethyl alcohol, Ran Houyong Nitrogen is dried up.DNA used sequence is AAAAATTTTT, 1- (3- dimethylamino-propyls) -3- ethyl carbodiimide salt in experiment The concentration of hydrochlorate is 0.05M.
The foregoing is only presently preferred embodiments of the present invention, all equivalent changes done according to scope of the present invention patent with Modification, should all belong to the covering scope of the present invention.

Claims (9)

1. a kind of preparation method of the orderly self-assembled structures of graphene/DNA, it is characterised in that this method comprises the following steps:
(1)Silicon chip polyglutamic acid or the polyacrylic acid solution immersion certain time of graphene will be loaded with, then spent respectively Ionized water, absolute ethyl alcohol are cleaned, and are then dried up with nitrogen;
(2)Be dissolved with 1- (3- dimethylamino-propyls) -3- ethyl-carbodiimide hydrochlorides solvent be 0.01M-0.1M PBS The single stranded DNA solution immersion of buffer solution, is then cleaned with deionized water, absolute ethyl alcohol, is then dried up with nitrogen, i.e., in stone respectively Black alkene surface forms the orderly self-assembled structures of DNA.
2. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that described negative The silicon chip of graphene is loaded with to peel off graphene onto silicon chip using micromechanical forces stripping method.
3. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 2, it is characterised in that described negative It is 1.0 × 10 that the silicon chip of graphene, which is loaded with, in 350 DEG C of -600 DEG C of vacuums-6Pa-1.0×10-4Vacuum annealing 2- is carried out under Pa 5h, to remove the cull remained on silicon chip.
4. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that 1- (3- Dimethylamino-propyl) -3- ethyl-carbodiimide hydrochlorides concentration be 0.01M-0.1M.
5. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that described poly- Glutamic acid or polyacrylic acid solution weight average molecular weight are that 20000-50000, concentration are 0.1 mg/ml-2mg/ml.
6. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that step (1) soak time is 0.5h-2h in.
7. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that the list Chain DNA sequence is AAAAATTTTT.
8. the preparation method of the orderly self-assembled structures of graphene/DNA according to claim 1, it is characterised in that step (2)Middle soak time is 6h-24h.
9. the orderly self-assembled structures of graphene/DNA prepared by a kind of method limited according to any one of claim 1-8.
CN201610159601.6A 2016-03-21 2016-03-21 Preparation method of graphene/DNA ordered self-assembly structure Expired - Fee Related CN107215860B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610159601.6A CN107215860B (en) 2016-03-21 2016-03-21 Preparation method of graphene/DNA ordered self-assembly structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610159601.6A CN107215860B (en) 2016-03-21 2016-03-21 Preparation method of graphene/DNA ordered self-assembly structure

Publications (2)

Publication Number Publication Date
CN107215860A true CN107215860A (en) 2017-09-29
CN107215860B CN107215860B (en) 2020-07-24

Family

ID=59927112

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610159601.6A Expired - Fee Related CN107215860B (en) 2016-03-21 2016-03-21 Preparation method of graphene/DNA ordered self-assembly structure

Country Status (1)

Country Link
CN (1) CN107215860B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109534349A (en) * 2018-03-30 2019-03-29 中国科学院上海应用物理研究所 A kind of synthetic method and application of organic mineralized structures based on frame nucleic acid encode

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101559944A (en) * 2009-05-27 2009-10-21 天津大学 Conductive graphene film and self-assembly preparation method thereof
CN102659918A (en) * 2012-05-16 2012-09-12 北京化工大学 Graphene/dipeptide self-assembly composite film and preparation method thereof
CN102875805A (en) * 2012-09-28 2013-01-16 浙江理工大学 Three-dimensional graphene-poly dopamine-gold nanoparticle composite material and preparation method thereof
CN102983291A (en) * 2012-11-27 2013-03-20 北京大学 Method for preparing molecular device with surficial biomolecules removed and based on graphene electrodes
CN103913496A (en) * 2014-02-28 2014-07-09 汕头大学 Preparation method and application of modified glassy carbon electrode

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101559944A (en) * 2009-05-27 2009-10-21 天津大学 Conductive graphene film and self-assembly preparation method thereof
CN102659918A (en) * 2012-05-16 2012-09-12 北京化工大学 Graphene/dipeptide self-assembly composite film and preparation method thereof
CN102875805A (en) * 2012-09-28 2013-01-16 浙江理工大学 Three-dimensional graphene-poly dopamine-gold nanoparticle composite material and preparation method thereof
CN102983291A (en) * 2012-11-27 2013-03-20 北京大学 Method for preparing molecular device with surficial biomolecules removed and based on graphene electrodes
CN103913496A (en) * 2014-02-28 2014-07-09 汕头大学 Preparation method and application of modified glassy carbon electrode

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
仇晓雯: "基于氧化石墨烯/金属纳米粒子的新型生物传感器研究", 《中国优秀硕士论文数据库》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109534349A (en) * 2018-03-30 2019-03-29 中国科学院上海应用物理研究所 A kind of synthetic method and application of organic mineralized structures based on frame nucleic acid encode

Also Published As

Publication number Publication date
CN107215860B (en) 2020-07-24

Similar Documents

Publication Publication Date Title
JP2017516296A5 (en)
JP2018120846A5 (en) Light emitting elements, light emitting devices, electronic devices and lighting devices
CN103627400B (en) Molybdenum alloy film and indium oxide film wet etchant component
JP2017517900A5 (en)
CN103342356B (en) Method for transferring graphene on metal foil substrate
JP2018510515A5 (en)
JP2011119548A5 (en)
JP2012169622A5 (en)
JP2005511808A5 (en)
JP2010083876A5 (en) Organic semiconductor material and electronic equipment
JP2010539991A5 (en)
US10804480B2 (en) Graphene laminate and preparation method therefor
CN103964413B (en) A kind of method improving carbon nanotube parallel array density
JP2017527674A5 (en)
JP6329330B1 (en) Sealing sheet and sealing body
WO2010051212A3 (en) Cyclic olefin compositions for temporary wafer bonding
JP2012025985A5 (en)
CN110669755B (en) Organic-inorganic hybrid nano flower and preparation method thereof
JP2011235532A5 (en)
JP2012004269A5 (en)
CN107215860A (en) A kind of preparation method of the orderly self-assembled structures of graphene/DNA
JPWO2014141998A1 (en) Charge transport varnish
JP2017525800A5 (en)
CN103935992A (en) Graphene transfer method
CN106699735A (en) Triazole compound and light-emitting device

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
GR01 Patent grant
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20200724

CF01 Termination of patent right due to non-payment of annual fee