Peptide having neuron loss prevention and regeneration effects and composition comprising same
A composition and an effective amount of technology are applied in the field of peptides with neuron loss prevention and regeneration effects and compositions containing the peptides, which can solve the problems that the correlation of human brain dysfunction is not clearly explained, and achieve the prevention of neuron loss. effect of loss
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Embodiment 1
[0137] Example 1: Peptide Synthesis
[0138] 1. Peptide Synthesis
[0139] The peptide of SEQ ID NO: 1 (hereinafter referred to as "PEP1") was prepared according to a conventionally known solid-phase peptide synthesis method. Specifically, peptides were synthesized by coupling each amino acid to another amino acid from the C-terminus by Fmoc solid-phase peptide synthesis (SPPS) using ASP48S (Peptron, Inc., Daejeon, Korea). Use a peptide where the first amino acid at the C-terminus is attached to the resin:
[0140] NH 2 -Lys(Boc)-2-chloro-trityl resin
[0141] NH 2 -Ala-2-chloro-trityl resin
[0142] NH 2 -Arg(Pbf)-2-chloro-trityl resin
[0143]In all amino acid compositions used for peptide synthesis, the N-terminus was protected with Fmoc, and the residues were protected with Trt, Boc, tert-butyl ester (t-Bu) and 2,2,4,6,7-pentamethyldihydro - Benzofuran-5-sulfonyl (Pbf) (which can be removed in acid) protection. Examples of amino acid compositions are as follows: ...
Embodiment 2
[0157] Embodiment 2: experimental preparation and material
Embodiment 2-1
[0158] Embodiment 2-1: the cultivation and processing of NSC and primary cortical nerve cells
[0159] All procedures involving animals were performed in accordance with the guidelines of the Animal Care and Use Committee of Hanyang University. All experiments were performed using a minimum number of animals with minimal pain, and all animals were used only once in an experiment.
[0160] NSCs were isolated from the brains of rat embryos, cultured and developed. NSC culture was performed in the same manner as will be described below. Briefly, rat embryos were obtained at embryonic day 13, and brains were rapidly removed and placed in petri dishes containing cold phosphate-buffered saline (Hank's balanced salt solution; HBSS).
[0161] Single cells were isolated from the cerebral cortex, lateral ganglionic eminence, and embryonic midbrain. Place these cells in culture dishes pretreated with L-ornithine and fibronectin containing phosphate-buffered saline (PBS) (without calci...
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