Rapid, enantioselective and colorimetric detection of D-arginine

Summary: D-amino acids are of biological significance yet are not clearly understood due to the lack of powerful analytical tools for their identification. Thus, the specific detection of a single enantiomer of a particular amino acid remains a great challenge due to their structural similarity. Her...

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Main Authors: Xianzhe Yu, Binjie Zhang, Cailing Fan, Qianqian Yan, Shenglin Wang, Hui Hu, Qinxi Dong, Gengyu Du, Yanan Gao, Chaoyuan Zeng
Format: Article
Language:English
Published: Elsevier 2022-09-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004222012366
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author Xianzhe Yu
Binjie Zhang
Cailing Fan
Qianqian Yan
Shenglin Wang
Hui Hu
Qinxi Dong
Gengyu Du
Yanan Gao
Chaoyuan Zeng
author_facet Xianzhe Yu
Binjie Zhang
Cailing Fan
Qianqian Yan
Shenglin Wang
Hui Hu
Qinxi Dong
Gengyu Du
Yanan Gao
Chaoyuan Zeng
author_sort Xianzhe Yu
collection DOAJ
description Summary: D-amino acids are of biological significance yet are not clearly understood due to the lack of powerful analytical tools for their identification. Thus, the specific detection of a single enantiomer of a particular amino acid remains a great challenge due to their structural similarity. Here, we report a strategy to incorporate multiple reaction sites on a chiral 1,1′-bi-2,2′-naphthol-based fluorescent probe. It can respond specifically to D-arginine, while producing no response when in contact with all other amino acids. The probe can report arginine’s concentration, and enantiomeric configuration and colorimetric studies enable its qualitative determination.
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spelling doaj.art-80d0c2251858464daf2aa5cd817d8cda2022-12-22T02:15:12ZengElsevieriScience2589-00422022-09-01259104964Rapid, enantioselective and colorimetric detection of D-arginineXianzhe Yu0Binjie Zhang1Cailing Fan2Qianqian Yan3Shenglin Wang4Hui Hu5Qinxi Dong6Gengyu Du7Yanan Gao8Chaoyuan Zeng9Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, ChinaDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA; Corresponding authorKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, China; Corresponding authorKey Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou 570228, China; Corresponding authorSummary: D-amino acids are of biological significance yet are not clearly understood due to the lack of powerful analytical tools for their identification. Thus, the specific detection of a single enantiomer of a particular amino acid remains a great challenge due to their structural similarity. Here, we report a strategy to incorporate multiple reaction sites on a chiral 1,1′-bi-2,2′-naphthol-based fluorescent probe. It can respond specifically to D-arginine, while producing no response when in contact with all other amino acids. The probe can report arginine’s concentration, and enantiomeric configuration and colorimetric studies enable its qualitative determination.http://www.sciencedirect.com/science/article/pii/S2589004222012366ChemistryAnalytical chemistryAnalytical chemistry applications
spellingShingle Xianzhe Yu
Binjie Zhang
Cailing Fan
Qianqian Yan
Shenglin Wang
Hui Hu
Qinxi Dong
Gengyu Du
Yanan Gao
Chaoyuan Zeng
Rapid, enantioselective and colorimetric detection of D-arginine
iScience
Chemistry
Analytical chemistry
Analytical chemistry applications
title Rapid, enantioselective and colorimetric detection of D-arginine
title_full Rapid, enantioselective and colorimetric detection of D-arginine
title_fullStr Rapid, enantioselective and colorimetric detection of D-arginine
title_full_unstemmed Rapid, enantioselective and colorimetric detection of D-arginine
title_short Rapid, enantioselective and colorimetric detection of D-arginine
title_sort rapid enantioselective and colorimetric detection of d arginine
topic Chemistry
Analytical chemistry
Analytical chemistry applications
url http://www.sciencedirect.com/science/article/pii/S2589004222012366
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