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Method for purification of quantum dot-streptavidin conjugate

A streptavidin and quantum dot technology, applied in chemical instruments and methods, peptide preparation methods, organic chemistry, etc., can solve problems such as difficulty in large-scale production, harsh operating conditions, and complex processes, and meet equipment requirements. Low, efficient separation, simple operation effect

Active Publication Date: 2014-03-26
NANCHANG UNIV
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  • Abstract
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  • Claims
  • Application Information

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Problems solved by technology

In short, although the above purification methods can be used to obtain high-quality quantum dot streptavidin conjugates, there are still defects such as harsh operating conditions, complicated processes, and low yields, and it is difficult to achieve large-scale production.

Method used

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  • Method for purification of quantum dot-streptavidin conjugate

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Embodiment 1

[0032] Embodiment 1 water-soluble quantum dot streptavidin conjugate and purification process

[0033] Take 5 mL of carboxylated water-soluble quantum dots (concentration: 50 nmol / L) and mix with an equal volume of 0.05 mol / L borate buffer at pH 5.0; add 1-ethyl -(3-Dimethylaminopropyl) carbodiimide and N-hydroxysulfosuccinimide, react at 37°C for 2 hours; add streptavidin solution with a molar ratio of 5:1 to quantum dots , adjust the pH of the solution to 8.0 with 1 M NaOH solution, react at room temperature for 3 hours; finally add polyethylene glycol with a final concentration of 1.5% to the solution, and further adjust the pH to 4.5 with 1 M HCl solution. 18,000 rpm (approx. 29,000 g) at 4°C for 30 min, discard the supernatant, and precipitate with 25% glycerol, 0.01% NaN 3 The water-soluble quantum dot streptavidin conjugate without free streptavidin was obtained by dissolving in 0.05 mol / L phosphate buffer (pH 7.0-7.5). After the water-soluble quantum dot streptavidin...

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Abstract

The invention discloses a new method suitable for large-scale high-efficiency purification of a water soluble quantum dot-streptavidin conjugate, and belongs to the field of biotechnology. In allusion to the disadvantages that a conventional quantum dot-streptavidin conjugate has complex purification process and low recovery rate and difficultly realizes large-scale production, single-terminal aminated polyethylene glycol (HO-PEG-NH3) is adopted to seal residual carboxyl of the quantum dot-streptavidin conjugate, a surface zeta potential of the conjugate is reduced; by adjusting the pH value of a solution to 4.5, the net charge content of the conjugate in the solution is further reduced, and the large-scale high-efficiency purification of the quantum dot-streptavidin conjugate is achieved by an ordinary high-speed centrifugation method. The method simplifies experimental operation procedures of the quantum dot-streptavidin conjugate, reduces requirements on separation equipment, is suitable for large-batch purification of the quantum dot-streptavidin conjugate, allows the yield to be more than 85%, and allows fluorescence characteristics and biological activity of the conjugate to have no significant changes.

Description

technical field [0001] The invention relates to a new method for biological modification of nanometer materials and purification of conjugates, in particular to a new method for large-scale and efficient purification of quantum dot and streptavidin conjugates. Background technique [0002] Streptavidin is a protein with similar biological characteristics to avidin, which can highly specifically bind a water-soluble vitamin: D-biotin. It has a very strong affinity with biotin, and the relationship between them The Kd value is close to 10 -15 M. Complete streptavidin is a tetramer composed of four identical peptide chains, with a total molecular weight of about 66.5kDa, and each streptavidin molecule can tightly bind four biotin molecules, with an average of each peptide chain ( monomer) can bind a biotin molecule. The complete tetramer streptavidin also has good thermal stability and strong tolerance to strong acids, sodium dodecylsulfonate, urea, and guanidine hydrochlori...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/36C07K1/14C07K1/13C09K11/02
CPCC07K14/36
Inventor 许恒毅熊勇华罗薇许杨赖卫华徐威
Owner NANCHANG UNIV
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