Fluorescence detecting glycopeptide antibiotics via a dynamic molecular switch.
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| Title: | Fluorescence detecting glycopeptide antibiotics via a dynamic molecular switch. |
|---|---|
| Authors: | Zou, Xiaomei1 (AUTHOR), Lin, Yanting2 (AUTHOR), Zhang, Shihui3 (AUTHOR), Deng, Tao4 (AUTHOR), Xu, Ximing5 (AUTHOR), Zhou, Yingchun1 (AUTHOR) yingchunbaby@126.com, Liu, Zhihui1 (AUTHOR), Lu, Weiguo1 (AUTHOR), Hu, Qingzhong2 (AUTHOR), Lin, Chaozhan2 (AUTHOR), Zhu, Chenchen1,2 (AUTHOR) zhucc@gzucm.edu.cn, Liu, Fang1,2 (AUTHOR) fangliu@gzucm.edu.cn |
| Source: | Analytica Chimica Acta. Mar2024, Vol. 1294, pN.PAG-N.PAG. 1p. |
| Subjects: | Glycopeptide antibiotics, Molecular switches, Rhodamines, Fluorescence, Fluorescent probes, Dynamic balance (Mechanics), Intramolecular proton transfer reactions |
| Abstract: | Glycopeptide antibiotics (GPAs) represented by vancomycin (VAN) are clinically used as a first-line treatment for serious infections caused by Gram-positive pathogens. The use and dosing methods of GPAs are rigorously managed for safety considerations, which calls for fast and accurate quantification approaches. A new sort of fluorescent probes for GPAs has been proposed, each of which was integrated by a fluorescein-based reporter and a GPAs' recognition peptide D-alanyl-D-alanine (D-Ala-D-Ala). These probes work as dynamic molecular switches, which mainly exist as non-fluorescent spirolactam forms in the absence of GPAs. GPAs binding with the dipeptide regulates the dynamic balance between fluorescence OFF lactam form and fluorescence ON ring-opened form, rendering these probes capable of GPAs detecting. The most promising one P1 exhibits excellent sensitivity and selectivity towards GPAs detection. Different to previous developments, P1 consists of a single fluorophore without the need of a fluorescence-quenching group or a secondary dye, which is the smallest fluorescent probe for GPAs up to now. P1 realizes direct VAN quantification from complex biological samples including real serums, dispensing with additional drug extraction. More interestingly, both P1 and P6 can distinguish GPAs with different peptide backbones, which has not been achieved previously. [Display omitted] • A new sort of fluorescent probes for glycopeptide antibiotics (GPAs) has been proposed. • Binding with GPAs will affect the dynamic switching by stabilizing the fluorescent-on form. • Probe P1 exhibited excellent sensitivity and selectivity for GPAs detection. • Probe P1 and P6 can distinguish GPAs with different backbones, which has not been achieved previously. [ABSTRACT FROM AUTHOR] |
| Copyright of Analytica Chimica Acta is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 175296383 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Fluorescence detecting glycopeptide antibiotics via a dynamic molecular switch. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zou%2C+Xiaomei%22">Zou, Xiaomei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Yanting%22">Lin, Yanting</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Shihui%22">Zhang, Shihui</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Deng%2C+Tao%22">Deng, Tao</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Ximing%22">Xu, Ximing</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhou%2C+Yingchun%22">Zhou, Yingchun</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> yingchunbaby@126.com</i><br /><searchLink fieldCode="AR" term="%22Liu%2C+Zhihui%22">Liu, Zhihui</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lu%2C+Weiguo%22">Lu, Weiguo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hu%2C+Qingzhong%22">Hu, Qingzhong</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Chaozhan%22">Lin, Chaozhan</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhu%2C+Chenchen%22">Zhu, Chenchen</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> zhucc@gzucm.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Liu%2C+Fang%22">Liu, Fang</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> fangliu@gzucm.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Analytica+Chimica+Acta%22">Analytica Chimica Acta</searchLink>. Mar2024, Vol. 1294, pN.PAG-N.PAG. 1p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Glycopeptide+antibiotics%22">Glycopeptide antibiotics</searchLink><br /><searchLink fieldCode="DE" term="%22Molecular+switches%22">Molecular switches</searchLink><br /><searchLink fieldCode="DE" term="%22Rhodamines%22">Rhodamines</searchLink><br /><searchLink fieldCode="DE" term="%22Fluorescence%22">Fluorescence</searchLink><br /><searchLink fieldCode="DE" term="%22Fluorescent+probes%22">Fluorescent probes</searchLink><br /><searchLink fieldCode="DE" term="%22Dynamic+balance+%28Mechanics%29%22">Dynamic balance (Mechanics)</searchLink><br /><searchLink fieldCode="DE" term="%22Intramolecular+proton+transfer+reactions%22">Intramolecular proton transfer reactions</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Glycopeptide antibiotics (GPAs) represented by vancomycin (VAN) are clinically used as a first-line treatment for serious infections caused by Gram-positive pathogens. The use and dosing methods of GPAs are rigorously managed for safety considerations, which calls for fast and accurate quantification approaches. A new sort of fluorescent probes for GPAs has been proposed, each of which was integrated by a fluorescein-based reporter and a GPAs' recognition peptide D-alanyl-D-alanine (D-Ala-D-Ala). These probes work as dynamic molecular switches, which mainly exist as non-fluorescent spirolactam forms in the absence of GPAs. GPAs binding with the dipeptide regulates the dynamic balance between fluorescence OFF lactam form and fluorescence ON ring-opened form, rendering these probes capable of GPAs detecting. The most promising one P1 exhibits excellent sensitivity and selectivity towards GPAs detection. Different to previous developments, P1 consists of a single fluorophore without the need of a fluorescence-quenching group or a secondary dye, which is the smallest fluorescent probe for GPAs up to now. P1 realizes direct VAN quantification from complex biological samples including real serums, dispensing with additional drug extraction. More interestingly, both P1 and P6 can distinguish GPAs with different peptide backbones, which has not been achieved previously. [Display omitted] • A new sort of fluorescent probes for glycopeptide antibiotics (GPAs) has been proposed. • Binding with GPAs will affect the dynamic switching by stabilizing the fluorescent-on form. • Probe P1 exhibited excellent sensitivity and selectivity for GPAs detection. • Probe P1 and P6 can distinguish GPAs with different backbones, which has not been achieved previously. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Analytica Chimica Acta is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.aca.2024.342309 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: N.PAG Subjects: – SubjectFull: Glycopeptide antibiotics Type: general – SubjectFull: Molecular switches Type: general – SubjectFull: Rhodamines Type: general – SubjectFull: Fluorescence Type: general – SubjectFull: Fluorescent probes Type: general – SubjectFull: Dynamic balance (Mechanics) Type: general – SubjectFull: Intramolecular proton transfer reactions Type: general Titles: – TitleFull: Fluorescence detecting glycopeptide antibiotics via a dynamic molecular switch. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zou, Xiaomei – PersonEntity: Name: NameFull: Lin, Yanting – PersonEntity: Name: NameFull: Zhang, Shihui – PersonEntity: Name: NameFull: Deng, Tao – PersonEntity: Name: NameFull: Xu, Ximing – PersonEntity: Name: NameFull: Zhou, Yingchun – PersonEntity: Name: NameFull: Liu, Zhihui – PersonEntity: Name: NameFull: Lu, Weiguo – PersonEntity: Name: NameFull: Hu, Qingzhong – PersonEntity: Name: NameFull: Lin, Chaozhan – PersonEntity: Name: NameFull: Zhu, Chenchen – PersonEntity: Name: NameFull: Liu, Fang IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 03 Text: Mar2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 00032670 Numbering: – Type: volume Value: 1294 Titles: – TitleFull: Analytica Chimica Acta Type: main |
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