Polypeptide sequence and preparation method and application of self-assembling material of polypeptide sequence
A technology for polypeptide sequence and self-assembly, applied in the field of its preparation and self-assembly of polypeptides, can solve problems such as pollution, and achieve the effects of low cost, convenient wide application and high stability
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Embodiment 2
[0037] Example 2: The polypeptide freeze-dried powder is dissolved in deionized water to configure a 200 μg / ml solution, the polypeptide is a soluble polypeptide, and the polypeptide solution is colorless and transparent. Take 5ml of the solution for circular dichroism detection. And calculate the percentage of various structures in the secondary structure of the polypeptide based on the detection results.
[0038] Circular dichroism (CD for short) is the most widely used method for determining the secondary structure of proteins, and it is a fast, simple and accurate method for studying protein conformation in dilute solutions.
Embodiment 3
[0039] Example 3: The polypeptide described herein was formulated into a 200 μg / ml solution, and the solution was colorless and transparent. Adding the disodium hydrogen phosphate that final concentration is 0.1M in the solution, visible white granular substance, the minimum concentration of disodium hydrogen phosphate that can form white granule is 5mM after testing. Aspirate 50 μl of the solution and place it on a glass slide, and take a cover glass to cover the droplet. Observe the results under an inverted microscope.
Embodiment 4
[0040] Example 4: The polypeptide described herein was formulated into a 200 μg / ml solution, and the solution was colorless and transparent. Disodium hydrogen phosphate was added to the solution to a final concentration of 0.1M. The sample is dropped on the copper sheet, and after drying, the copper sheet loaded with the sample is stuck on the conductive tape on the sample holder. Step by step for photo shooting.
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