Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus
Astragalus membranaceus root, Huang Qi in Chinese, is a popular medicinal herb traditionally used to regulate blood glucose. Herein, the identification and characterization of two families of cysteine-rich peptides (CRPs), designated α- and β-astratides, from A. membranaceus roots are reported. Prot...
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sg-ntu-dr.10356-1469702021-03-16T02:07:38Z Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus Huang, Jiayi Wong, Ka Ho Tay, Stephanie Victoria Serra, Aida Sze, Siu Kuan Tam, James P. School of Biological Sciences Science::Biological sciences Protein-structure Antimicrobial Peptides Astragalus membranaceus root, Huang Qi in Chinese, is a popular medicinal herb traditionally used to regulate blood glucose. Herein, the identification and characterization of two families of cysteine-rich peptides (CRPs), designated α- and β-astratides, from A. membranaceus roots are reported. Proteomic analysis showed that α-astratide aM1 and β-astratide bM1 belong to two distinct CRP families. The six-cysteine-containing and proline-rich α-astratide aM1 displayed high sequence identity to Pea Albumin 1 Subunit b (PA1b), while the eight-cysteine-containing β-astratide bM1 showed sequence similarity to plant defensins. An antifungal assay revealed that bM1 possessed potent antifungal activity. In contrast, aM1 showed a cytotoxic effect against insect Sf9 cells. More importantly, aM1 decreased insulin secretion in mouse pancreatic β cells, suggesting it could interfere in glucose homeostasis, which accounts for the adaptogenic property of A. membranaceus. Phylogenetic clustering analysis suggested that the proline-rich aM1 is a putative prolyl oligopeptidase inhibitor and belongs to a novel subfamily of PA1b-like peptides, while bM1 belongs to a new subfamily of plant defensins. Together, the study reveals that astratides are multifunctional CRPs in plants, which expand the existing library of PA1b-like peptides and plant defensins and further our understanding of their roles in host-defense system and leads as peptidyl therapeutics. Ministry of Education (MOE) National Research Foundation (NRF) This research was in part by the Competitive Research Grant by supported by National Research Foundation in Singapore (NRF-CRP8-2011-05), a Nanyang Technological University internal funding−Synzyme and Natural Products Center (SYNC) and the AcRF Tier 3 funding (MOE2016-T3-1- 003).We would like to thank Dr Yan Zhao from School of Biological Sciences, Nanyang Technological University, Singapore for the authentication of plant sample Astragalus membranaceus. 2021-03-16T02:07:38Z 2021-03-16T02:07:38Z 2019 Journal Article Huang, J., Wong, K. H., Tay, S. V., Serra, A., Sze, S. K. & Tam, J. P. (2019). Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus. Journal of Natural Products, 82(2), 194-204. https://dx.doi.org/10.1021/acs.jnatprod.8b00521 0163-3864 https://hdl.handle.net/10356/146970 10.1021/acs.jnatprod.8b00521 30758201 2-s2.0-85061924094 2 82 194 204 en NRF-CRP8-2011-05 MOE2016-T3-1- 003 Journal of Natural Products © 2019 American Chemical Society and American Society of Pharmacognosy. All rights reserved. |
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Science::Biological sciences Protein-structure Antimicrobial Peptides Huang, Jiayi Wong, Ka Ho Tay, Stephanie Victoria Serra, Aida Sze, Siu Kuan Tam, James P. Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
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Astragalus membranaceus root, Huang Qi in Chinese, is a popular medicinal herb traditionally used to regulate blood glucose. Herein, the identification and characterization of two families of cysteine-rich peptides (CRPs), designated α- and β-astratides, from A. membranaceus roots are reported. Proteomic analysis showed that α-astratide aM1 and β-astratide bM1 belong to two distinct CRP families. The six-cysteine-containing and proline-rich α-astratide aM1 displayed high sequence identity to Pea Albumin 1 Subunit b (PA1b), while the eight-cysteine-containing β-astratide bM1 showed sequence similarity to plant defensins. An antifungal assay revealed that bM1 possessed potent antifungal activity. In contrast, aM1 showed a cytotoxic effect against insect Sf9 cells. More importantly, aM1 decreased insulin secretion in mouse pancreatic β cells, suggesting it could interfere in glucose homeostasis, which accounts for the adaptogenic property of A. membranaceus. Phylogenetic clustering analysis suggested that the proline-rich aM1 is a putative prolyl oligopeptidase inhibitor and belongs to a novel subfamily of PA1b-like peptides, while bM1 belongs to a new subfamily of plant defensins. Together, the study reveals that astratides are multifunctional CRPs in plants, which expand the existing library of PA1b-like peptides and plant defensins and further our understanding of their roles in host-defense system and leads as peptidyl therapeutics. |
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School of Biological Sciences |
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School of Biological Sciences Huang, Jiayi Wong, Ka Ho Tay, Stephanie Victoria Serra, Aida Sze, Siu Kuan Tam, James P. |
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Article |
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Huang, Jiayi Wong, Ka Ho Tay, Stephanie Victoria Serra, Aida Sze, Siu Kuan Tam, James P. |
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Huang, Jiayi |
title |
Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
title_short |
Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
title_full |
Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
title_fullStr |
Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
title_full_unstemmed |
Astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from Astragalus membranaceus |
title_sort |
astratides : insulin-modulating, insecticidal, and antifungal cysteine-rich peptides from astragalus membranaceus |
publishDate |
2021 |
url |
https://hdl.handle.net/10356/146970 |
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1695706219700813824 |