Method for observing separation of micro-nano scale protein crystals from solution

A Micro-Nano-Scale, Protein Crystallization Technology

Inactive Publication Date: 2016-04-20
北京达尔文细胞生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the second harmonic technique can only be used to detect crystals with low symmetry or large size; the intensity of fluorescence in UV fluorescence method depends on the number of aromatic residues or disulfide bonds in the po

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Example 1: Detect whether there are micro-nano scale lysozyme crystals precipitated from the crystallization solution

[0023] The first step: drop the crystallization solution; first, drop the lysozyme crystallization solution into the quartz pool (height 20mm, bottom thickness 4mm, pool wall thickness 13.8mm, internal thickness 3mm), seal it, and carry out the experiment under normal temperature conditions;

[0024] The second step: adjust the mutual extinction of the two polarizers: first, turn on the laser light source, and the natural light emitted by it passes through the first polarizer to become linearly polarized light; then, the polarized light passes through the quartz crystal pool to reach the second linear polarizer, It is found that the light intensity is 0.05mV, indicating that the two polarizers are not completely extinguished; adjust the second linear polarizer until the light intensity is 0.01mV;

[0025] Step 3: Observe whether there are crystals: before

Embodiment 2

[0026] Example 2: Detecting whether there are proteinase K crystals of micro-nano scale separated out from the crystallization solution

[0027] The first step: drop the crystallization solution; first, drop the lysozyme crystallization solution into the quartz pool (height 20mm, bottom thickness 4mm, pool wall thickness 9.8mm, internal thickness 2mm), seal it, and carry out the experiment under normal temperature conditions;

[0028] Step 2: Adjust the mutual extinction of the two polarizers: first, turn on the laser light source, and the laser light passes through the first polarizer to become linearly polarized light; then, the polarized light passes through the quartz crystal cell to reach the second linear polarizer, and the light intensity is 0.02mV, indicating that the two polarizers have been completely extinguished;

[0029] Step 3: Observe whether there are crystals: before crystals are precipitated, the laser passes through the linear polarizer-quartz pool-crystallizat

Embodiment 3

[0030] Embodiment 3: Detect whether there are micro-nano scale catalase crystals separated out from the crystallization solution

[0031] The first step: drop the crystallization solution; first, drop the catalase crystallization solution into the plexiglass and seal it; then place the beaker between two semiconductor refrigerators, precisely control the temperature of the experiment, and adjust the experimental temperature to 0 ℃.

[0032] The second step: adjust the mutual extinction of the two polarizers: first, turn on the laser light source, and the natural light emitted by it passes through the first polarizer to become linearly polarized light; then, the polarized light passes through the quartz crystal pool to reach the second linear polarizer, It is found that the light intensity is 0.1mV, indicating that the two polarizers are not completely extinguished;

[0033]Step 3: Observe whether there are crystals appearing: before crystals are precipitated, the laser passes th

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Abstract

The invention provides a method for observing separation of micro-nano scale protein crystals from solution. A protein crystallization solution is added into a quartz crystallization pond dropwise, and the quartz crystallization pond is sealed; then, the quartz crystallization pond is placed between two wire polarizers, laser sequentially penetrates through the first wire polarizer, the quartz crystallization pond and the second wire polarizer, and the two wire polarizers are adjusted till the intensity of light measured by a light intensity tester is 0-0.02 mV; the light intensity measured by the light intensity tester is observed, and it is determined that crystals appear when the light intensity is larger than 0.02 mV. Whether mini-crystals are formed in the crystallization solution or not can be observed in real time, and the method has the advantages of being easy to operate, capable of achieving real-time observation, efficient and the like.

Description

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Claims

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Application Information

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Owner 北京达尔文细胞生物科技有限公司
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