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Pentosinane, a Post-Translational Modification of Human Proteins with Underappreciated Stability

Overview
Journal J Am Chem Soc
Specialty Chemistry
Date 2022 Nov 21
PMID 36410375
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Abstract

Pentosinane is a structurally complex nonenzymatic post-translational modification of proteins believed to be present in all living things. It falls into the category of advanced glycation end products (AGEs) and is structurally related to the other AGEs pentosidine and glucosepane. Although pentosidine and glucosepane have been widely studied for their role in wide-ranging conditions (e.g., diabetes mellitus, Alzheimer's disease, and human aging), relatively little is known about pentosinane. Interestingly, previous reports have suggested that pentosidine may derive from pentosinane. The (patho)physiological significance of pentosinane in humans is largely unexplored. As a first step to address this knowledge gap, we report herein the first total synthesis of pentosinane. Our synthesis is high yielding (1.7% over seven steps), concise, and enantioselective, and it leverages a strategy for synthesizing 2,5-diaminoimidazoles previously developed by our lab. Access to synthetic pentosinane has allowed us to perform additional studies showing that its oxidation to pentosidine is both pH and oxygen dependent and is substantially slower under physiological conditions than previously believed. Additionally, pentosinane rapidly decomposes under harshly acidic conditions typically employed for pentosidine isolation. Taken together, these results suggest that pentosinane is likely to be more abundant than previously appreciated. We believe these results represent a critical step toward illuminating the role(s) of pentosinane in human biology.

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References
1.
Lee R, Bashrum B, Cagle E, Walters J, Massey J, Zanghi M . Electronic Donation or Steric Contraction: A Spectroscopic and Structural Analysis of Medium-Sized Constrained Rings for Potential Long-Range Hyperconjugation. J Org Chem. 2019; 84(16):9897-9906. DOI: 10.1021/acs.joc.9b00979. View

2.
Sell D, Nagaraj R, Grandhee S, Odetti P, Lapolla A, Fogarty J . Pentosidine: a molecular marker for the cumulative damage to proteins in diabetes, aging, and uremia. Diabetes Metab Rev. 1991; 7(4):239-51. DOI: 10.1002/dmr.5610070404. View

3.
Draghici C, Wang T, Spiegel D . Concise total synthesis of glucosepane. Science. 2015; 350(6258):294-8. DOI: 10.1126/science.aac9655. View

4.
Friedlander M, Wu Y, Schulak J, Monnier V, Hricik D . Influence of dialysis modality on plasma and tissue concentrations of pentosidine in patients with end-stage renal disease. Am J Kidney Dis. 1995; 25(3):445-51. DOI: 10.1016/0272-6386(95)90107-8. View

5.
Piarulli F, Sartore G, Ceriello A, Ragazzi E, Reitano R, Nollino L . Relationship between glyco-oxidation, antioxidant status and microalbuminuria in type 2 diabetic patients. Diabetologia. 2009; 52(7):1419-25. DOI: 10.1007/s00125-009-1367-y. View