Literature DB >> 22944686

Current and prospective applications of non-proteinogenic amino acids in profiling of proteases substrate specificity.

Paulina Kasperkiewicz1, Anna D Gajda, Marcin Drąg.   

Abstract

Proteases recognize their endogenous substrates based largely on a sequence of proteinogenic amino acids that surrounds the cleavage site. Currently, several methods are available to determine protease substrate specificity based on approaches employing proteinogenic amino acids. The knowledge about the specificity of proteases can be significantly extended by application of structurally diverse families of non-proteinogenic amino acids. From a chemical point of view, this information may be used to design specific substrates, inhibitors, or activity-based probes, while biological functions of proteases, such as posttranslational modifications can also be investigated. In this review, we discuss current and prospective technologies for application of non-proteinogenic amino acids in protease substrate specificity profiling.

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Year:  2012        PMID: 22944686     DOI: 10.1515/hsz-2012-0167

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  9 in total

1.  Protease cleavage site fingerprinting by label-free in-gel degradomics reveals pH-dependent specificity switch of legumain.

Authors:  Robert Vidmar; Matej Vizovišek; Dušan Turk; Boris Turk; Marko Fonović
Journal:  EMBO J       Date:  2017-07-21       Impact factor: 11.598

2.  Design of ultrasensitive probes for human neutrophil elastase through hybrid combinatorial substrate library profiling.

Authors:  Paulina Kasperkiewicz; Marcin Poreba; Scott J Snipas; Heather Parker; Christine C Winterbourn; Guy S Salvesen; Marcin Drag
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

Review 3.  Small Molecule Active Site Directed Tools for Studying Human Caspases.

Authors:  Marcin Poreba; Aleksandra Szalek; Paulina Kasperkiewicz; Wioletta Rut; Guy S Salvesen; Marcin Drag
Journal:  Chem Rev       Date:  2015-11-09       Impact factor: 60.622

4.  Synthesis of a HyCoSuL peptide substrate library to dissect protease substrate specificity.

Authors:  Marcin Poreba; Guy S Salvesen; Marcin Drag
Journal:  Nat Protoc       Date:  2017-09-21       Impact factor: 13.491

5.  Photoactivatable Reporter to Perform Multiplexed and Temporally Controlled Measurements of Kinase and Protease Activity in Single Cells.

Authors:  Matthew M Anttila; Brianna M Vickerman; Qunzhao Wang; David S Lawrence; Nancy L Allbritton
Journal:  Anal Chem       Date:  2021-12-04       Impact factor: 6.986

6.  The Staphylococcus aureus leucine aminopeptidase is localized to the bacterial cytosol and demonstrates a broad substrate range that extends beyond leucine.

Authors:  Ronan K Carroll; Florian Veillard; Danielle T Gagne; Jarrod M Lindenmuth; Marcin Poreba; Marcin Drag; Jan Potempa; Lindsey N Shaw
Journal:  Biol Chem       Date:  2013-06       Impact factor: 3.915

7.  Sequence-derived structural features driving proteolytic processing.

Authors:  Alexander A Belushkin; Dmitry V Vinogradov; Mikhail S Gelfand; Andrei L Osterman; Piotr Cieplak; Marat D Kazanov
Journal:  Proteomics       Date:  2013-12-11       Impact factor: 3.984

8.  Synthesis of fluorescent (benzyloxycarbonylamino)(aryl)methylphosphonates.

Authors:  Michał Górny Vel Górniak; Anna Czernicka; Piotr Młynarz; Waldemar Balcerzak; Paweł Kafarski
Journal:  Beilstein J Org Chem       Date:  2014-03-28       Impact factor: 2.883

9.  A remarkable activity of human leukotriene A4 hydrolase (LTA4H) toward unnatural amino acids.

Authors:  Anna Byzia; Jesper Z Haeggström; Guy S Salvesen; Marcin Drag
Journal:  Amino Acids       Date:  2014-02-27       Impact factor: 3.520

  9 in total

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