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肽作为代谢与心血管相互作用关键调节因子的发现。

Discovery of peptides as key regulators of metabolic and cardiovascular crosstalk.

作者信息

Zhang Zeyuan, Svensson Katrin J

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA; Stanford Diabetes Research Center, Stanford University, Stanford, CA, USA; Stanford Cardiovascular Institute, Stanford University, Stanford, CA, USA.

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA; Stanford Diabetes Research Center, Stanford University, Stanford, CA, USA; Stanford Cardiovascular Institute, Stanford University, Stanford, CA, USA.

出版信息

Cell Rep. 2025 Jun 24;44(6):115836. doi: 10.1016/j.celrep.2025.115836. Epub 2025 Jun 16.

Abstract

Peptides are fundamental regulators of metabolism, with several already developed as drugs, including glucagon-like peptide-1-based peptide therapeutics for diabetes and obesity. Despite their established importance, our understanding of their biosynthesis, modifications, receptor interactions, and signaling pathways remains incomplete. Advances in peptidomics and proteomics, particularly mass spectrometry, have facilitated peptide discovery and characterization, revealing novel roles for known peptides and uncovering previously unrecognized post-translational modifications. With the increasing prevalence of metabolic diseases driven by obesity, understanding the regulatory functions of peptide hormones has significant therapeutic potential. This review discusses the latest insights into peptide biology, highlighting key examples of peptides controlling tissue crosstalk, as well as how multi-omics technologies, computational approaches, and AI-driven methods are likely to expand our knowledge of peptide-mediated metabolic regulation.

摘要

肽是新陈代谢的基本调节因子,已有几种肽被开发为药物,包括用于治疗糖尿病和肥胖症的基于胰高血糖素样肽-1的肽疗法。尽管它们的重要性已得到确立,但我们对其生物合成、修饰、受体相互作用和信号通路的理解仍不完整。肽组学和蛋白质组学的进展,尤其是质谱技术,促进了肽的发现和表征,揭示了已知肽的新作用,并发现了以前未被认识的翻译后修饰。随着肥胖导致的代谢性疾病日益普遍,了解肽激素的调节功能具有重大的治疗潜力。本综述讨论了肽生物学的最新见解,重点介绍了控制组织间相互作用的肽的关键实例,以及多组学技术、计算方法和人工智能驱动的方法如何可能扩展我们对肽介导的代谢调节的认识。

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