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claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide

[Image: see text] Molecularly targeted research and diagnostic tools are essential to advancing understanding and detection of many diseases. Metals often impart the desired functionality to these tools, and conjugation of high-affinity chelators to proteins is carried out to enable targeted deliver...

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Autores principales: Mills, Brittney J., Mu, Qingxin, Krause, Mary E., Laurence, Jennifer S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215913/
https://www.ncbi.nlm.nih.gov/pubmed/24807049
http://dx.doi.org/10.1021/bc500115h
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author Mills, Brittney J.
Mu, Qingxin
Krause, Mary E.
Laurence, Jennifer S.
author_facet Mills, Brittney J.
Mu, Qingxin
Krause, Mary E.
Laurence, Jennifer S.
author_sort Mills, Brittney J.
collection PubMed
description [Image: see text] Molecularly targeted research and diagnostic tools are essential to advancing understanding and detection of many diseases. Metals often impart the desired functionality to these tools, and conjugation of high-affinity chelators to proteins is carried out to enable targeted delivery of the metal. This approach has been much more effective with large lanthanide series metals than smaller transition metals. Because chemical conjugation requires additional processing and purification steps and yields a heterogeneous mixture of products, inline incorporation of a peptide tag capable of metal binding is a highly preferable alternative. Development of a transition metal binding tag would provide opportunity to greatly expand metal-based analyses. The metal abstraction peptide (MAP) sequence was genetically engineered into recombinant protein to generate the claMP Tag. The effects of this tag on recombinant epidermal growth factor (EGF) protein expression, disulfide bond formation, tertiary structural integrity, and transition metal incorporation using nickel were examined to confirm the viability of utilizing the MAP sequence to generate linker-less metal conjugates.
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spelling pubmed-42159132015-05-07 claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide Mills, Brittney J. Mu, Qingxin Krause, Mary E. Laurence, Jennifer S. Bioconjug Chem [Image: see text] Molecularly targeted research and diagnostic tools are essential to advancing understanding and detection of many diseases. Metals often impart the desired functionality to these tools, and conjugation of high-affinity chelators to proteins is carried out to enable targeted delivery of the metal. This approach has been much more effective with large lanthanide series metals than smaller transition metals. Because chemical conjugation requires additional processing and purification steps and yields a heterogeneous mixture of products, inline incorporation of a peptide tag capable of metal binding is a highly preferable alternative. Development of a transition metal binding tag would provide opportunity to greatly expand metal-based analyses. The metal abstraction peptide (MAP) sequence was genetically engineered into recombinant protein to generate the claMP Tag. The effects of this tag on recombinant epidermal growth factor (EGF) protein expression, disulfide bond formation, tertiary structural integrity, and transition metal incorporation using nickel were examined to confirm the viability of utilizing the MAP sequence to generate linker-less metal conjugates. American Chemical Society 2014-05-07 2014-06-18 /pmc/articles/PMC4215913/ /pubmed/24807049 http://dx.doi.org/10.1021/bc500115h Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Mills, Brittney J.
Mu, Qingxin
Krause, Mary E.
Laurence, Jennifer S.
claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title_full claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title_fullStr claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title_full_unstemmed claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title_short claMP Tag: A Versatile Inline Metal-Binding Platform Based on the Metal Abstraction Peptide
title_sort clamp tag: a versatile inline metal-binding platform based on the metal abstraction peptide
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215913/
https://www.ncbi.nlm.nih.gov/pubmed/24807049
http://dx.doi.org/10.1021/bc500115h
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