Literature DB >> 20731990

Chapter 3. High-throughput protein purification for x-ray crystallography and NMR.

Youngchang Kim1, Lance Bigelow, Maria Borovilos, Irina Dementieva, Erika Duggan, William Eschenfeldt, Catherine Hatzos, Grazyna Joachimiak, Hui Li, Natalia Maltseva, Rory Mulligan, Pearl Quartey, Alicia Sather, Lucy Stols, Lour Volkart, Ruiying Wu, Min Zhou, Andrzej Joachimiak.   

Abstract

In structural biology, the most critical issue is the availability of high-quality samples. "Structural-biology-grade" proteins must be generated in a quantity and quality suitable for structure determination using X-ray crystallography or nuclear magnetic resonance. The additional challenge for structural genomics is the need for high numbers of proteins at low cost where protein targets quite often have low sequence similarities, unknown properties and are poorly characterized. The purification procedures must reproducibly yield homogeneous proteins or their derivatives containing marker atom(s) in milligram quantities. The choice of protein purification and handling procedures plays a critical role in obtaining high-quality protein samples. Where the ultimate goal of structural biology is the same-to understand the structural basis of proteins in cellular processes, the structural genomics approach is different in that the functional aspects of individual protein or family are not ignored, however, emphasis here is on the number of unique structures, covering most of the protein folding space and developing new technologies with high efficiency. At the Midwest Center Structural Genomics (MCSG), we have developed semiautomated protocols for high-throughput parallel protein purification. In brief, a protein, expressed as a fusion with a cleavable affinity tag, is purified in two immobilized metal affinity chromatography (IMAC) steps: (i) first IMAC coupled with buffer-exchange step, and after tag cleavage using TEV protease, (ii) second IMAC and buffer exchange to clean up cleaved tags and tagged TEV protease. Size exclusion chromatography is also applied as needed. These protocols have been implemented on multidimensional chromatography workstations AKTAexplorer and AKTAxpress (GE Healthcare). All methods and protocols used for purification, some developed in MCSG, others adopted and integrated into the MCSG purification pipeline and more recently the Center for Structural Genomics of Infectious Disease (CSGID) purification pipeline, are discussed in this chapter.

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Year:  2009        PMID: 20731990      PMCID: PMC3366499          DOI: 10.1016/S0065-3233(07)75003-9

Source DB:  PubMed          Journal:  Adv Protein Chem Struct Biol        ISSN: 1876-1623            Impact factor:   3.507


  23 in total

1.  A new vector for high-throughput, ligation-independent cloning encoding a tobacco etch virus protease cleavage site.

Authors:  Lucy Stols; Minyi Gu; Lynda Dieckman; Rosemarie Raffen; Frank R Collart; Mark I Donnelly
Journal:  Protein Expr Purif       Date:  2002-06       Impact factor: 1.650

2.  A less laborious approach to the high-throughput production of recombinant proteins in Escherichia coli using 2-liter plastic bottles.

Authors:  Cynthia Sanville Millard; Lucy Stols; Pearl Quartey; Youngchang Kim; Irina Dementieva; Mark I Donnelly
Journal:  Protein Expr Purif       Date:  2003-06       Impact factor: 1.650

3.  Automation of protein purification for structural genomics.

Authors:  Youngchang Kim; Irina Dementieva; Min Zhou; Ruiying Wu; Lour Lezondra; Pearl Quartey; Grazyna Joachimiak; Olga Korolev; Hui Li; Andrzej Joachimiak
Journal:  J Struct Funct Genomics       Date:  2004

4.  High-throughput automated refolding screening of inclusion bodies.

Authors:  Renaud Vincentelli; Stéphane Canaan; Valérie Campanacci; Christel Valencia; Damien Maurin; Frédéric Frassinetti; Loréna Scappucini-Calvo; Yves Bourne; Christian Cambillau; Christophe Bignon
Journal:  Protein Sci       Date:  2004-10       Impact factor: 6.725

5.  On-column protein refolding for crystallization.

Authors:  Natalia Oganesyan; Sung-Hou Kim; Rosalind Kim
Journal:  J Struct Funct Genomics       Date:  2005

6.  Molecular genetic and biochemical evidence for the involvement of the heptapeptide cleavage sequence in determining the reaction profile at two tobacco etch virus cleavage sites in cell-free assays.

Authors:  W G Dougherty; T D Parks
Journal:  Virology       Date:  1989-09       Impact factor: 3.616

7.  Use of bacteriophage T7 lysozyme to improve an inducible T7 expression system.

Authors:  F W Studier
Journal:  J Mol Biol       Date:  1991-05-05       Impact factor: 5.469

8.  Production of selenomethionine-labeled proteins in two-liter plastic bottles for structure determination.

Authors:  Lucy Stols; Cynthia Sanville Millard; Irina Dementieva; Mark I Donnelly
Journal:  J Struct Funct Genomics       Date:  2004

9.  Production in two-liter beverage bottles of proteins for NMR structure determination labeled with either 15N- or 13C-15N.

Authors:  Qin Zhao; Ronnie Frederick; Kory Seder; Sandy Thao; Hassan Sreenath; Francis Peterson; Brian F Volkman; John L Markley; Brian G Fox
Journal:  J Struct Funct Genomics       Date:  2004

10.  Artificial chaperone-assisted refolding of carbonic anhydrase B.

Authors:  D Rozema; S H Gellman
Journal:  J Biol Chem       Date:  1996-02-16       Impact factor: 5.157

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  21 in total

1.  Large scale structural rearrangement of a serine hydrolase from Francisella tularensis facilitates catalysis.

Authors:  Ekaterina V Filippova; Leigh A Weston; Misty L Kuhn; Brett Geissler; Alexandra M Gehring; Nicola Armoush; Chinessa T Adkins; George Minasov; Ievgeniia Dubrovska; Ludmilla Shuvalova; James R Winsor; Luke D Lavis; Karla J F Satchell; Daniel P Becker; Wayne F Anderson; R Jeremy Johnson
Journal:  J Biol Chem       Date:  2013-02-19       Impact factor: 5.157

2.  Crystal Structures of the SpoIID Lytic Transglycosylases Essential for Bacterial Sporulation.

Authors:  Salvatore Nocadello; George Minasov; Ludmilla S Shuvalova; Ievgeniia Dubrovska; Elisabetta Sabini; Wayne F Anderson
Journal:  J Biol Chem       Date:  2016-05-18       Impact factor: 5.157

3.  A novel polyamine allosteric site of SpeG from Vibrio cholerae is revealed by its dodecameric structure.

Authors:  Ekaterina V Filippova; Misty L Kuhn; Jerzy Osipiuk; Olga Kiryukhina; Andrzej Joachimiak; Miguel A Ballicora; Wayne F Anderson
Journal:  J Mol Biol       Date:  2015-01-23       Impact factor: 5.469

Review 4.  Design of Experiments As a Tool for Optimization in Recombinant Protein Biotechnology: From Constructs to Crystals.

Authors:  Christos Papaneophytou
Journal:  Mol Biotechnol       Date:  2019-12       Impact factor: 2.695

5.  A conserved surface loop in type I dehydroquinate dehydratases positions an active site arginine and functions in substrate binding.

Authors:  Samuel H Light; George Minasov; Ludmilla Shuvalova; Scott N Peterson; Michael Caffrey; Wayne F Anderson; Arnon Lavie
Journal:  Biochemistry       Date:  2011-02-21       Impact factor: 3.162

6.  Insights into the mechanism of type I dehydroquinate dehydratases from structures of reaction intermediates.

Authors:  Samuel H Light; George Minasov; Ludmilla Shuvalova; Mark-Eugene Duban; Michael Caffrey; Wayne F Anderson; Arnon Lavie
Journal:  J Biol Chem       Date:  2010-11-18       Impact factor: 5.157

7.  Protein production for structural genomics using E. coli expression.

Authors:  Magdalena Makowska-Grzyska; Youngchang Kim; Natalia Maltseva; Hui Li; Min Zhou; Grazyna Joachimiak; Gyorgy Babnigg; Andrzej Joachimiak
Journal:  Methods Mol Biol       Date:  2014

8.  Expression, purification, crystallization and preliminary X-ray crystallographic analysis of the L,D-transpeptidase LdtMt1 from Mycobacterium tuberculosis.

Authors:  Stefania Correale; Alessia Ruggiero; Emilia Pedone; Rita Berisio
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2013-02-22

9.  The Protein Maker: an automated system for high-throughput parallel purification.

Authors:  Eric R Smith; Darren W Begley; Vanessa Anderson; Amy C Raymond; Taryn E Haffner; John I Robinson; Thomas E Edwards; Natalie Duncan; Cory J Gerdts; Mark B Mixon; Peter Nollert; Bart L Staker; Lance J Stewart
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2011-08-13

Review 10.  An overview of enzymatic reagents for the removal of affinity tags.

Authors:  David S Waugh
Journal:  Protein Expr Purif       Date:  2011-08-19       Impact factor: 1.650

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