Method for screening crude delta sleep-inducing peptide extract from milk source in virtue of patch clamp technique
A patch clamp technique and sleep-promoting technology, which is applied in the field of separation and purification of sleep-promoting peptides, can solve the problems of lack of high-quality stereo microscopes and water immersion objectives, not widely used, lack of models, etc., to reduce production costs and simple operation , the effect of increasing the sample volume
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Embodiment 1
[0026] Add 100L of pure water to the reaction vessel, heat to 55°C, add 12KG of milk protein, adjust the pH of the solution to 8, start stirring at 300rpm, add 36g of trypsin, and enzymatically hydrolyze for 3 hours to inactivate the enzyme. Add 12g of pepsin, adjust the pH to 5, adjust the temperature to 40°C, and perform enzymatic hydrolysis for 2 hours. After enzymatic hydrolysis, the enzyme was inactivated, the temperature was adjusted to 90°C, and the temperature was kept for 30 minutes. Then adjust the pH of the filtrate to 5, add ethanol to a concentration of 70%, stir well, after 3 hours of precipitation, stand at 4°C for 4 hours, then filter the supernatant, collect the precipitate, dry the precipitate at 55-65°C, and obtain the casein hydrolysis product , high purity, light bitter and salty taste, good color, yield 2.35kg.
[0027] Using ShimadzuPRC-ODS (K) steel column, the above-mentioned isolated and purified product is separated and purified through the preparat...
Embodiment 2
[0030] Take out rats born about 5 weeks old, weighing about 100g-150g, acutely separate their hypothalamus, slice the hypothalamus into 400um slices, and quickly put them into a tube filled with 95% O 2 and 5% artificial cerebrospinal fluid, incubate at 33°C for 30min, take out the incubation tank, and place at room temperature for 20min. A cored hard glass blank with an outer diameter of 1.4mm is used. After polishing, the tip is drawn to a diameter of about 2um and filled with the electrode inner liquid. First observe the structure of the hypothalamus with a 5× objective lens to find the ventrolateral preoptic area, then observe the morphology of a single ventrolateral preoptic area neuron with a 40× water immersion lens and seal it with electrodes. When the tip of the electrode and the cell form After successful sealing of more than 1GΩ, the whole cell mode is formed after the cells are observed to charge and discharge capacitance in the sealing window. First record a blank...
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