Modulation of insulin receptor activation through controlled folding of peptide ligands

Insulin receptor (IR) activation requires coordinated engagement of two distinct insulin-binding sites, and recent structural insights have highlighted the role of a disulfide bond in IR agonist S597 in the S597-IR complex. In this study, we synthesized and evaluated analogs of S597 and the IR antagonist Ins-AC-S2, replacing their native disulfide bridges with alternative linkages. While these modifications had minimal impact on Ins-AC-S2's antagonistic activity, they significantly reduced the agonistic potency of S597, suggesting that conformational stability is critical for receptor activation. Our findings provide a structural basis for designing non-insulin ligands to selectively activate or inhibit the insulin receptor, with potential therapeutic implications.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00363f
Citations
2
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
4.01
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article

Modulation of insulin receptor activation through controlled folding of peptide ligands

Nai-Pin Lin, Yuankun Dao, Maxwell J. Austin, Danny Hung‐Chieh Chou et al.
2 citations
Organic & Biomolecular Chemistry
Pancreatic function and diabetes
4.01
article

Modulation of insulin receptor activation through controlled folding of peptide ligands

Nai-Pin Lin, Yuankun Dao, Maxwell J. Austin, Danny Hung‐Chieh Chou, Wenchao Li, Terra Lin
article en
2 citations

Abstract

Insulin receptor (IR) activation requires coordinated engagement of two distinct insulin-binding sites, and recent structural insights have highlighted the role of a disulfide bond in IR agonist S597 in the S597-IR complex. In this study, we synthesized and evaluated analogs of S597 and the IR antagonist Ins-AC-S2, replacing their native disulfide bridges with alternative linkages. While these modifications had minimal impact on Ins-AC-S2's antagonistic activity, they significantly reduced the agonistic potency of S597, suggesting that conformational stability is critical for receptor activation. Our findings provide a structural basis for designing non-insulin ligands to selectively activate or inhibit the insulin receptor, with potential therapeutic implications.

Organic & Biomolecular ChemistryVol. 23(19)
Diabetes Australia (AU), Stanford University (US)
Openalex Percentile: Top 8%
Pancreatic function and diabetes
4.01
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