Design of Histidine Sequence‐Associated Tripeptide Sequences for Recognition of Copper Ions and Their Application to Live Cells
ABSTRACT Copper is central to many enzymes in living organisms, and imbalances in copper levels are linked to various diseases. Therefore, developing probes to detect copper ions is essential. Histidine, especially in the polypeptide sequences at the first three N‐terminal positions (His1, His2, and...
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Published in | Luminescence (Chichester, England) Vol. 40; no. 2; pp. e70095 - n/a |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.02.2025
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Subjects | |
Online Access | Get full text |
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Summary: | ABSTRACT
Copper is central to many enzymes in living organisms, and imbalances in copper levels are linked to various diseases. Therefore, developing probes to detect copper ions is essential. Histidine, especially in the polypeptide sequences at the first three N‐terminal positions (His1, His2, and His3), uniquely binds to copper ions. This study introduces three groups of tripeptide probes designed to monitor copper ion levels in living cells and organisms. The results show that tripeptides with histidine at the −2 position, specifically HDQL‐2 (Asp‐His‐Gln‐Dansyl), HMFM‐2 (Met‐His‐Phe‐Dansyl), and HDMB‐2 (Asp‐His‐Met‐Dansyl), exhibit a higher affinity for copper ions. These probes responded quickly to copper ions, demonstrating excellent fluorescence turn‐off performance and stable detection within a pH range of 6.0–11.0. The detection limits for fluorescence titration, calculated using the 3σ/k equation, were 17.65 nM (HDQL‐2), 18.04 nM (HMFM‐2), and 15.50 nM (HDMB‐2). Peptide probes are ideal for detecting copper ions in living cells via fluorescence imaging because of their low toxicity and good biocompatibility. The fluorescence intensity decreases as copper ion content changes.
This study designs three tripeptide probes (HDQL‐2, HMFM‐2, and HDMB‐2) to monitor copper ion levels in living cells and organisms. These probes, with histidine at the −2 position, bind efficiently to copper ions, showing a rapid fluorescence turn‐off response across a pH range of 6.0–11.0. Detection limits for copper ions were 17.65 nM (HDQL‐2), 18.04 nM (HMFM‐2), and 15.50 nM (HDMB‐2), making them suitable for fluorescence imaging with low toxicity and good biocompatibility. |
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Bibliography: | This work was supported by the Natural Science Foundation of Jiangxi Province (20212ACB206026), Key Technology Research and Application of Shijiazhuang high‐level scientific and technological innovation and entrepreneurial talents (08202301), Key Technology Research and Application of New Tibetan Medicine Preparation (2023ZY016), and ShangDa Translational Medicine Funding supported by Wenzhou Institute of Shanghai University (SDTMF2023KP03). Funding Xue‐jiao Wang and Jun‐lei Hao contributed equally to this work ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1522-7235 1522-7243 1522-7243 |
DOI: | 10.1002/bio.70095 |