一种核桃粕抗结肠癌肽及其应用

Walnut meal protein peptide VSLP was prepared and screened by enzymatic hydrolysis. Combined with network pharmacology and molecular docking methods, it solved the problems of adverse reactions and low bioavailability of existing anticancer drugs, and achieved high-efficiency inhibition and apoptosis induction of colon cancer cells, providing a safe and effective anticancer treatment option.

CN116425831BActive Publication Date: 2026-07-17YUNNAN AGRICULTURAL UNIVERSITY

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
YUNNAN AGRICULTURAL UNIVERSITY
Filing Date
2023-05-31
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing anticancer drugs have adverse effects on organs such as the kidneys, heart, and gonads. Furthermore, long-term use can lead to multiple drug resistance, low drug bioavailability, and poor cell specificity, resulting in an increased probability of cancer recurrence. Moreover, existing methods are not efficient at screening peptides with anti-colon cancer activity.

Method used

Walnut meal peptides were prepared by enzymatic hydrolysis and purified by ultrafiltration. Val-Ser-Leu-Pro (VSLP), a walnut meal protein peptide with anti-colon cancer activity, was screened using network pharmacology, bioinformatics, and molecular docking methods. Targets were predicted using the SwissADME, Swiss Target Prediction, GeneCards, Drugbank, and DisGeNET databases. A target network was constructed using CytoScape, and functional annotation and pathway enrichment were performed using the David database. Molecular docking was used to verify the binding of the peptides to the targets.

Benefits of technology

The screened walnut meal protein peptide VSLP showed significant inhibitory effects on the proliferation of human colon cancer HCT116 cells, with an IC50 value of 214.9 μM. It also showed strong inhibitory activity against other colon cancer cell lines, achieving anti-cancer effects by inducing apoptosis and inhibiting proliferation.

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Abstract

本发明公开了一种核桃粕抗结肠癌肽及其应用,属于食品深加工技术领域。所述抗结肠癌细胞增殖肽自C端至N端的氨基酸序列为:Val‑Ser‑Leu‑Pro,简称VSLP。本发明从核桃粕中酶解制备了抗结肠癌细胞增殖肽,采用超滤进行纯化,经nanao‑LC‑MS / MS鉴定多肽序列,并利用网络药理学、生物信息学和分子对接技术筛选抗结肠癌细胞增殖肽,筛选出的抗结肠癌肽VSLP与结肠癌关键靶点CASP‑3和MMP‑9之间主要通过氢键和疏水相互作用。人工合成并验证了所述肽抗结肠癌细胞增殖活性,多肽VSLP可以有效抑制人结肠癌HCT116、HT‑29、SW480和SW620细胞系增殖。
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