Implementation of semi-automated cloning and prokaryotic expression screening: the impact of SPINE.

The implementation of high-throughput (HTP) cloning and expression screening in Escherichia coli by 14 laboratories in the Structural Proteomics In Europe (SPINE) consortium is described. Cloning efficiencies of greater than 80% have been achieved for the three non-ligation-based cloning techniques used, namely Gateway, ligation-indendent cloning of PCR products (LIC-PCR) and In-Fusion, with LIC-PCR emerging as the most cost-effective. On average, two constructs have been made for each of the approximately 1700 protein targets selected by SPINE for protein production. Overall, HTP expression screening in E. coli has yielded 32% soluble constructs, with at least one for 70% of the targets. In addition to the implementation of HTP cloning and expression screening, the development of two novel technologies is described, namely library-based screening for soluble constructs and parallel small-scale high-density fermentation.

[1]  Joel Moss,et al.  Rapid, reliable ligation-independent cloning of PCR products using modified plasmid vectors. , 1992, BioTechniques.

[2]  Victor H Hernandez,et al.  Nature Methods , 2007 .

[3]  J. Betton,et al.  High throughput cloning and expression strategies for protein production. , 2004, Biochimie.

[4]  M. Vidal,et al.  GATEWAY recombinational cloning: application to the cloning of large numbers of open reading frames or ORFeomes. , 2000, Methods in enzymology.

[5]  F. Studier,et al.  Protein production by auto-induction in high density shaking cultures. , 2005, Protein expression and purification.

[6]  R. Esnouf,et al.  Structure of a functional IGF2R fragment determined from the anomalous scattering of sulfur , 2002, The EMBO journal.

[7]  P. D. de Jong,et al.  Ligation-independent cloning of PCR products (LIC-PCR). , 1990, Nucleic acids research.

[8]  D. Smith,et al.  Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase. , 1988, Gene.

[9]  Renaud Vincentelli,et al.  High‐throughput automated refolding screening of inclusion bodies , 2004, Protein science : a publication of the Protein Society.

[10]  V. Garsky,et al.  Cleavage of small peptides in vitro by human rhinovirus 14 3C protease expressed in Escherichia coli , 1989, Journal of virology.

[11]  Martin Hammarström,et al.  Rapid screening for improved solubility of small human proteins produced as fusion proteins in Escherichia coli , 2002, Protein science : a publication of the Protein Society.

[12]  J. LaBaer,et al.  Many paths to many clones: a comparative look at high-throughput cloning methods. , 2004, Genome research.

[13]  D. Moras,et al.  Construction of a set Gateway-based destination vectors for high-throughput cloning and expression screening in Escherichia coli. , 2005, Analytical biochemistry.

[14]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[15]  Yan-Ping Shih,et al.  High‐throughput screening of soluble recombinant proteins , 2002, Protein science : a publication of the Protein Society.

[16]  J. Hartley,et al.  DNA cloning using in vitro site-specific recombination. , 2000, Genome research.

[17]  C. Glover,et al.  Gene expression profiling for hematopoietic cell culture , 2006 .

[18]  Christian Cambillau,et al.  Crystal structure of the conserved hypothetical protein Rv1155 from Mycobacterium tuberculosis , 2005, FEBS letters.

[19]  Narayanan Eswar,et al.  High-throughput computational and experimental techniques in structural genomics. , 2004, Genome research.

[20]  P. Nordlund,et al.  Screening for soluble expression of recombinant proteins in a 96-well format. , 2001, Analytical biochemistry.

[21]  S. A. Johnston,et al.  Release of proteins and peptides from fusion proteins using a recombinant plant virus proteinase. , 1994, Analytical biochemistry.

[22]  R. Vincentelli,et al.  Automated expression and solubility screening of His-tagged proteins in 96-well format. , 2005, Analytical biochemistry.

[23]  J. Janin,et al.  The Paris-Sud yeast structural genomics pilot-project: from structure to function. , 2004, Biochimie.

[24]  B. Neilan,et al.  Enzyme-free cloning of PCR products and fusion protein expression. , 2002, Methods in molecular biology.

[25]  Renaud Vincentelli,et al.  Medium-scale structural genomics: strategies for protein expression and crystallization. , 2003, Accounts of chemical research.

[26]  M. Saraste,et al.  FEBS Lett , 2000 .