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Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins

Squaramate‐linked 2′‐deoxycytidine 5′‐O‐triphosphate was synthesized and found to be good substrate for KOD XL DNA polymerase in primer extension or PCR synthesis of modified DNA. The resulting squaramate‐linked DNA reacts with primary amines to form a stable diamide linkage. This reaction was used...

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Detalles Bibliográficos
Autores principales: Ivancová, Ivana, Pohl, Radek, Hubálek, Martin, Hocek, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771961/
https://www.ncbi.nlm.nih.gov/pubmed/31328344
http://dx.doi.org/10.1002/anie.201906737
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author Ivancová, Ivana
Pohl, Radek
Hubálek, Martin
Hocek, Michal
author_facet Ivancová, Ivana
Pohl, Radek
Hubálek, Martin
Hocek, Michal
author_sort Ivancová, Ivana
collection PubMed
description Squaramate‐linked 2′‐deoxycytidine 5′‐O‐triphosphate was synthesized and found to be good substrate for KOD XL DNA polymerase in primer extension or PCR synthesis of modified DNA. The resulting squaramate‐linked DNA reacts with primary amines to form a stable diamide linkage. This reaction was used for bioconjugations of DNA with Cy5 and Lys‐containing peptides. Squaramate‐linked DNA formed covalent cross‐links with histone proteins. This reactive nucleotide has potential for other bioconjugations of nucleic acids with amines, peptides or proteins without need of any external reagent.
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spelling pubmed-67719612019-10-07 Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins Ivancová, Ivana Pohl, Radek Hubálek, Martin Hocek, Michal Angew Chem Int Ed Engl Communications Squaramate‐linked 2′‐deoxycytidine 5′‐O‐triphosphate was synthesized and found to be good substrate for KOD XL DNA polymerase in primer extension or PCR synthesis of modified DNA. The resulting squaramate‐linked DNA reacts with primary amines to form a stable diamide linkage. This reaction was used for bioconjugations of DNA with Cy5 and Lys‐containing peptides. Squaramate‐linked DNA formed covalent cross‐links with histone proteins. This reactive nucleotide has potential for other bioconjugations of nucleic acids with amines, peptides or proteins without need of any external reagent. John Wiley and Sons Inc. 2019-08-13 2019-09-16 /pmc/articles/PMC6771961/ /pubmed/31328344 http://dx.doi.org/10.1002/anie.201906737 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Ivancová, Ivana
Pohl, Radek
Hubálek, Martin
Hocek, Michal
Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title_full Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title_fullStr Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title_full_unstemmed Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title_short Squaramate‐Modified Nucleotides and DNA for Specific Cross‐Linking with Lysine‐Containing Peptides and Proteins
title_sort squaramate‐modified nucleotides and dna for specific cross‐linking with lysine‐containing peptides and proteins
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771961/
https://www.ncbi.nlm.nih.gov/pubmed/31328344
http://dx.doi.org/10.1002/anie.201906737
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