Highlights
• Novel methods to prepare higher anti-hyperuricemia activity peptides were proposed.
• Bioinformatics strategies in screening anti-hyperuricemia peptides were recommended.
• Classical uric acid homeostasis- and novel microbiota-based mechanism was discussed.
• Structure-activity relationships of anti-hyperuricemia peptides were summarized.
• Future prospectives in peptides bioavailability improvement were also mentioned.
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