Chemistry in living systems. Prescher, J. A & Bertozzi, C. R Nature Chemical Biology, 1(1):13--21, June, 2005. ![Chemistry in living systems [link]](https://bibbase.org/img/filetypes/link.svg "link")
Paper doi abstract bibtex Dissecting complex cellular processes requires the ability to track biomolecules as they function within their native habitat. Although genetically encoded tags such as GFP are widely used to monitor discrete proteins, they can cause significant perturbations to a protein's structure and have no direct extension to other classes of biomolecules such as glycans, lipids, nucleic acids and secondary metabolites. In recent years, an alternative tool for tagging biomolecules has emerged from the chemical biology community--the bioorthogonal chemical reporter. In a prototypical experiment, a unique chemical motif, often as small as a single functional group, is incorporated into the target biomolecule using the cell's own biosynthetic machinery. The chemical reporter is then covalently modified in a highly selective fashion with an exogenously delivered probe. This review highlights the development of bioorthogonal chemical reporters and reactions and their application in living systems.
@article{prescher_chemistry_2005,
title = {Chemistry in living systems},
volume = {1},
issn = {1552-4450},
url = {http://www.ncbi.nlm.nih.gov/pubmed/16407987},
doi = {10.1038/nchembio0605-13},
abstract = {Dissecting complex cellular processes requires the ability to track biomolecules as they function within their native habitat. Although genetically encoded tags such as GFP are widely used to monitor discrete proteins, they can cause significant perturbations to a protein's structure and have no direct extension to other classes of biomolecules such as glycans, lipids, nucleic acids and secondary metabolites. In recent years, an alternative tool for tagging biomolecules has emerged from the chemical biology community--the bioorthogonal chemical reporter. In a prototypical experiment, a unique chemical motif, often as small as a single functional group, is incorporated into the target biomolecule using the cell's own biosynthetic machinery. The chemical reporter is then covalently modified in a highly selective fashion with an exogenously delivered probe. This review highlights the development of bioorthogonal chemical reporters and reactions and their application in living systems.},
number = {1},
urldate = {2009-05-03TZ},
journal = {Nature Chemical Biology},
author = {Prescher, Jennifer A and Bertozzi, Carolyn R},
month = jun,
year = {2005},
pmid = {16407987},
keywords = {Animals, Cells, Cultured, Green Fluorescent Proteins, Lipids, Molecular Probe Techniques, Molecular Probes, Polysaccharides, Proteins},
pages = {13--21}
}
Downloads: 0
{"_id":"fPtke8yDmMLorBamH","bibbaseid":"prescher-bertozzi-chemistryinlivingsystems-2005","downloads":0,"creationDate":"2017-04-04T08:13:35.752Z","title":"Chemistry in living systems","author_short":["Prescher, J. A","Bertozzi, C. R"],"year":2005,"bibtype":"article","biburl":"http://bibbase.org/zotero/velocityhughes","bibdata":{"bibtype":"article","type":"article","title":"Chemistry in living systems","volume":"1","issn":"1552-4450","url":"http://www.ncbi.nlm.nih.gov/pubmed/16407987","doi":"10.1038/nchembio0605-13","abstract":"Dissecting complex cellular processes requires the ability to track biomolecules as they function within their native habitat. Although genetically encoded tags such as GFP are widely used to monitor discrete proteins, they can cause significant perturbations to a protein's structure and have no direct extension to other classes of biomolecules such as glycans, lipids, nucleic acids and secondary metabolites. In recent years, an alternative tool for tagging biomolecules has emerged from the chemical biology community--the bioorthogonal chemical reporter. In a prototypical experiment, a unique chemical motif, often as small as a single functional group, is incorporated into the target biomolecule using the cell's own biosynthetic machinery. The chemical reporter is then covalently modified in a highly selective fashion with an exogenously delivered probe. This review highlights the development of bioorthogonal chemical reporters and reactions and their application in living systems.","number":"1","urldate":"2009-05-03TZ","journal":"Nature Chemical Biology","author":[{"propositions":[],"lastnames":["Prescher"],"firstnames":["Jennifer","A"],"suffixes":[]},{"propositions":[],"lastnames":["Bertozzi"],"firstnames":["Carolyn","R"],"suffixes":[]}],"month":"June","year":"2005","pmid":"16407987","keywords":"Animals, Cells, Cultured, Green Fluorescent Proteins, Lipids, Molecular Probe Techniques, Molecular Probes, Polysaccharides, Proteins","pages":"13--21","bibtex":"@article{prescher_chemistry_2005,\n\ttitle = {Chemistry in living systems},\n\tvolume = {1},\n\tissn = {1552-4450},\n\turl = {http://www.ncbi.nlm.nih.gov/pubmed/16407987},\n\tdoi = {10.1038/nchembio0605-13},\n\tabstract = {Dissecting complex cellular processes requires the ability to track biomolecules as they function within their native habitat. Although genetically encoded tags such as GFP are widely used to monitor discrete proteins, they can cause significant perturbations to a protein's structure and have no direct extension to other classes of biomolecules such as glycans, lipids, nucleic acids and secondary metabolites. In recent years, an alternative tool for tagging biomolecules has emerged from the chemical biology community--the bioorthogonal chemical reporter. In a prototypical experiment, a unique chemical motif, often as small as a single functional group, is incorporated into the target biomolecule using the cell's own biosynthetic machinery. The chemical reporter is then covalently modified in a highly selective fashion with an exogenously delivered probe. This review highlights the development of bioorthogonal chemical reporters and reactions and their application in living systems.},\n\tnumber = {1},\n\turldate = {2009-05-03TZ},\n\tjournal = {Nature Chemical Biology},\n\tauthor = {Prescher, Jennifer A and Bertozzi, Carolyn R},\n\tmonth = jun,\n\tyear = {2005},\n\tpmid = {16407987},\n\tkeywords = {Animals, Cells, Cultured, Green Fluorescent Proteins, Lipids, Molecular Probe Techniques, Molecular Probes, Polysaccharides, Proteins},\n\tpages = {13--21}\n}\n\n","author_short":["Prescher, J. A","Bertozzi, C. R"],"key":"prescher_chemistry_2005","id":"prescher_chemistry_2005","bibbaseid":"prescher-bertozzi-chemistryinlivingsystems-2005","role":"author","urls":{"Paper":"http://www.ncbi.nlm.nih.gov/pubmed/16407987"},"keyword":["Animals","Cells","Cultured","Green Fluorescent Proteins","Lipids","Molecular Probe Techniques","Molecular Probes","Polysaccharides","Proteins"],"downloads":0},"search_terms":["chemistry","living","systems","prescher","bertozzi"],"keywords":["animals","cells","cultured","green fluorescent proteins","lipids","molecular probe techniques","molecular probes","polysaccharides","proteins"],"authorIDs":[],"dataSources":["QQyXj7M8pdnbq89aP"]}