Graftable SCoMPIs enable the labeling and X-ray fluorescence imaging of proteins-Reference-Cited by-同舟云学术

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Graftable SCoMPIs enable the labeling and X-ray fluorescence imaging of proteins

Published:2018 Issue:19 Volume:9 Page:4483-4487
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Hostachy Sarah¹²³⁴⁵,Masuda Marie⁶⁷⁸⁹¹⁰,Miki Takayuki⁶⁷⁸⁹¹⁰^ORCID,Hamachi Itaru⁶⁷⁸⁹¹⁰^ORCID,Sagan Sandrine⁵³⁴¹¹¹,Lequin Olivier⁵³⁴¹¹¹^ORCID,Medjoubi Kadda¹²¹³¹⁴,Somogyi Andrea¹²¹³¹⁴,Delsuc Nicolas¹²³⁴⁵^ORCID,Policar Clotilde¹²³⁴⁵^ORCID

Affiliation:

1. Laboratoire des Biomolécules, LBM

2. Département de Chimie

3. École Normale Supérieure

4. PSL University

5. Sorbonne Université

6. Department of Synthetic Chemistry and Biological Chemistry

7. Graduate School of Engineering

8. Kyoto University

9. Kyoto 615-8510

10. Japan

11. CNRS

12. Nanoscopium Synchrotron SOLEIL Saint-Aubin

13. Gif-sur-Yvette Cedex

14. France

Abstract

Sensitive detection of proteins by X-ray fluorescence microspectroscopy using the Re core of a single core multimodal probe for imaging.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/SC/C8SC00886H

Reference48 articles.

1. How to unveil self-quenched fluorophores and subsequently map the subcellular distribution of exogenous peptides

2. Influence of the Side-Chain Length on the Cellular Uptake and the Cytotoxicity of Rhenium Triscarbonyl Derivatives: A Bimodal Infrared and Luminescence Quantitative Study

3. A Bis(dipyridophenazine)(2-(2-pyridyl)pyrimidine-4-carboxylic acid)ruthenium(II) Complex with Anticancer Action upon Photodeprotection

4. Quantitative fluorescence spectroscopy and flow cytometry analyses of cell-penetrating peptides internalization pathways: optimization, pitfalls, comparison with mass spectrometry quantification

5. FT-IR spectroscopic investigations of single cells on the subcellular level

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