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Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes

Two photo‐crosslinking biarsenical (CrAsH‐EDT(2))‐modified probes were synthesized that are expected to be useful tools for tetracysteine‐labeled proteins to facilitate the co‐affinity purification of their DNA binding sequences and interacting proteins. In addition, improvements for the synthesis o...

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Autores principales: Syeda, Shameem S., Rice, Daren, Hook, Derek J., Heckert, Leslie L., Georg, Gunda I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069617/
https://www.ncbi.nlm.nih.gov/pubmed/26948688
http://dx.doi.org/10.1002/ardp.201500440
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author Syeda, Shameem S.
Rice, Daren
Hook, Derek J.
Heckert, Leslie L.
Georg, Gunda I.
author_facet Syeda, Shameem S.
Rice, Daren
Hook, Derek J.
Heckert, Leslie L.
Georg, Gunda I.
author_sort Syeda, Shameem S.
collection PubMed
description Two photo‐crosslinking biarsenical (CrAsH‐EDT(2))‐modified probes were synthesized that are expected to be useful tools for tetracysteine‐labeled proteins to facilitate the co‐affinity purification of their DNA binding sequences and interacting proteins. In addition, improvements for the synthesis of CrAsH‐EDT(2) and N (1)‐(4‐azido‐2‐nitrophenyl)hexane‐1,6‐diamine are reported. Both photoprobes effectively entered HeLa cells (and the nucleus) and were dependent on the tetracysteine motif in recombinant DMRT1 (doublesex and Mab3‐related transcription factor) to induce fluorescence, suggesting that their crosslinking abilities can be exploited for the identification of nucleic acids and proteins associated with a protein of interest.
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spelling pubmed-50696172016-11-01 Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes Syeda, Shameem S. Rice, Daren Hook, Derek J. Heckert, Leslie L. Georg, Gunda I. Arch Pharm (Weinheim) Full Papers Two photo‐crosslinking biarsenical (CrAsH‐EDT(2))‐modified probes were synthesized that are expected to be useful tools for tetracysteine‐labeled proteins to facilitate the co‐affinity purification of their DNA binding sequences and interacting proteins. In addition, improvements for the synthesis of CrAsH‐EDT(2) and N (1)‐(4‐azido‐2‐nitrophenyl)hexane‐1,6‐diamine are reported. Both photoprobes effectively entered HeLa cells (and the nucleus) and were dependent on the tetracysteine motif in recombinant DMRT1 (doublesex and Mab3‐related transcription factor) to induce fluorescence, suggesting that their crosslinking abilities can be exploited for the identification of nucleic acids and proteins associated with a protein of interest. John Wiley and Sons Inc. 2016-03-07 2016-04 /pmc/articles/PMC5069617/ /pubmed/26948688 http://dx.doi.org/10.1002/ardp.201500440 Text en © 2016 The Authors. Archiv der Pharmazie Published by Wiley‐VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Syeda, Shameem S.
Rice, Daren
Hook, Derek J.
Heckert, Leslie L.
Georg, Gunda I.
Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title_full Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title_fullStr Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title_full_unstemmed Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title_short Synthesis of Arylazide‐ and Diazirine‐Containing CrAsH‐EDT(2) Photoaffinity Probes
title_sort synthesis of arylazide‐ and diazirine‐containing crash‐edt(2) photoaffinity probes
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069617/
https://www.ncbi.nlm.nih.gov/pubmed/26948688
http://dx.doi.org/10.1002/ardp.201500440
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