4.7 Article

Characterization of dietary and herbal sourced natural compounds that modulate SEL1L-HRD1 ERAD activity and alleviate protein misfolding in the ER

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JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 111, 期 -, 页码 -

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2022.109178

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Peptide hormones; ERAD; Drug screening; Natural compounds; Cryptochlorogenic acid

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Dysregulated production of peptide hormones can lead to various endocrine diseases. Endoplasmic reticulum associated degradation (ERAD) plays a crucial role in maintaining ER proteostasis by degrading misfolded proteins. Targeting ERAD for regulating peptide hormone production is limited, and herbal products provide potential alternative therapeutics. In this study, a virtual screening was performed to identify compounds targeting SEL1L-HRD1 ERAD machinery, and Cryptochlorogenic acid (CCA) was found to enhance ERAD activity and promote the secretion of well-folded peptide hormone. These findings contribute to drug discovery strategies for targeting ER protein homeostasis and provide candidate compounds for hormone-related diseases.
Dysregulated production of peptide hormones is the key pathogenic factor of various endocrine diseases. Endoplasmic reticulum (ER) associated degra-dation (ERAD) is a critical machinery in maintaining ER proteostasis in mammalian cells by degrading misfolded proteins. Dysfunction of ERAD leads to maturation defect of many peptide hormones, such as provasopressin (proAVP), which results in the occurrence of Central Diabetes Insipidus. However, drugs targeting ERAD to regulate the production of peptide hormones are very limited. Herbal products provide not only nutritional sources, but also alternative therapeutics for chronic diseases. Virtual screening provides an effective and high-throughput strategy for identifying protein structure-based interacting compounds extracted from a variety of dietary or herbal sources, which could be served as (pro)drugs for preventing or treating endocrine diseases. Here, we performed a virtual screening by directly targeting SEL1L of the most conserved SEL1L-HRD1 ERAD machinery. Further, we analyzed 58 top-ranked compounds and demonstrated that Cryptochlorogenic acid (CCA) showed strong affinity with the binding pocket of SEL1L with HRD1. Through structure-based docking, protein expression assays, and FACS analysis, we revealed that CCA enhanced ERAD activity and promoted the degradation of mis-folded proAVP, thus facilitated the secretion of well-folded proAVP. These results provide us with insights into drug discovery strategies targeting ER protein homeostasis, as well as candidate compounds for treating hormone-related diseases. (c) 2022 Elsevier Inc. All rights reserved.

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