Literature DB >> 12622154

Caging proteins through unnatural amino acid mutagenesis.

E James Petersson1, Gabriel S Brandt, Niki M Zacharias, Dennis A Dougherty, Henry A Lester.   

Abstract

The caging of specific residues of proteins is a powerful tool. This discussion attempts to alert the reader to the considerations that must be made in preparing and analyzing a caged protein through nonsense suppression. Although the suppression methodology is conceptually straightforward, it not possible to provide a failsafe "cook book" method for using caged unnaturals. We have emphasized the preparation of caged receptors expressed in Xenopus oocytes, but these approaches can clearly be adapted to many other systems.

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Year:  2003        PMID: 12622154     DOI: 10.1016/s0076-6879(03)60114-x

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  5 in total

1.  Caged compounds: photorelease technology for control of cellular chemistry and physiology.

Authors:  Graham C R Ellis-Davies
Journal:  Nat Methods       Date:  2007-08       Impact factor: 28.547

Review 2.  Recent advances in the photochemical control of protein function.

Authors:  Chad W Riggsbee; Alexander Deiters
Journal:  Trends Biotechnol       Date:  2010-07-29       Impact factor: 19.536

Review 3.  In vivo incorporation of non-canonical amino acids by using the chemical aminoacylation strategy: a broadly applicable mechanistic tool.

Authors:  Dennis A Dougherty; Ethan B Van Arnam
Journal:  Chembiochem       Date:  2014-07-02       Impact factor: 3.164

4.  Light-mediated liberation of enzymatic activity: "small molecule" caged protein equivalents.

Authors:  Haishan Li; Jung-Mi Hah; David S Lawrence
Journal:  J Am Chem Soc       Date:  2008-07-19       Impact factor: 15.419

5.  Allosteric regulation in NMDA receptors revealed by the genetically encoded photo-cross-linkers.

Authors:  Meilin Tian; Shixin Ye
Journal:  Sci Rep       Date:  2016-10-07       Impact factor: 4.379

  5 in total

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