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Updated: May 28, 2026

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High-Throughput Expression and Purification of Human Solute Carriers for Structural and Biochemical Studies
Published on: September 29, 2023
Urate transporters: an evolving field.
1Department of Pharmacology and Toxicology, Dokkyo Medical University School of Medicine, Shimotsuga, Tochigi, Japan.
Seminars in Nephrology
|October 18, 2011
Summary
Uric acid, a product of purine metabolism, can cause diseases like gout when levels are too high. Understanding how the body handles uric acid is key to managing these conditions.
Area of Science:
- Biochemistry
- Human Physiology
- Genetics
Background:
- Uric acid is the end product of purine metabolism in humans.
- Hyperuricemia is linked to gout, kidney disease, hypertension, and cardiovascular issues.
- The kidney is crucial for regulating serum urate levels via excretion.
Purpose of the Study:
- To review the molecular mechanisms of renal urate handling.
- To explore the roles of urate transporters in various human tissues.
- To provide a comprehensive overview of transmembrane urate transport.
Main Methods:
- Review of scientific literature.
- Analysis of findings from genome-wide association studies (GWAS).
- Discussion of identified urate transport-related genes and proteins.
Main Results:
- URAT1 (SLC22A12) was identified in 2002, advancing understanding of urate transport.
- GWAS have linked serum urate levels to single nucleotide polymorphisms in multiple genetic loci.
- Evidence suggests urate transporters play roles in extrarenal tissues, including the intestine.
Conclusions:
- Despite progress, the complete picture of renal urate handling remains unclear.
- Further research into urate transporters in both renal and extrarenal tissues is warranted.
- Understanding these transport mechanisms is vital for addressing hyperuricemia-related diseases.
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