Literature DB >> 16211503

Structural genomics of eukaryotic targets at a laboratory scale.

Didier Busso1, Pierre Poussin-Courmontagne, David Rosé, Raymond Ripp, Alain Litt, Jean-Claude Thierry, Dino Moras.   

Abstract

Structural genomics programs are distributed worldwide and funded by large institutions such as the NIH in United-States, the RIKEN in Japan or the European Commission through the SPINE network in Europe. Such initiatives, essentially managed by large consortia, led to technology and method developments at the different steps required to produce biological samples compatible with structural studies. Besides specific applications, method developments resulted mainly upon miniaturization and parallelization. The challenge that academic laboratories faces to pursue structural genomics programs is to produce, at a higher rate, protein samples. The Structural Biology and Genomics Department (IGBMC - Illkirch - France) is implicated in a structural genomics program of high eukaryotes whose goal is solving crystal structures of proteins and their complexes (including large complexes) related to human health and biotechnology. To achieve such a challenging goal, the Department has established a medium-throughput pipeline for producing protein samples suitable for structural biology studies. Here, we describe the setting up of our initiative from cloning to crystallization and we demonstrate that structural genomics may be manageable by academic laboratories by strategic investments in robotic and by adapting classical bench protocols and new developments, in particular in the field of protein expression, to parallelization.

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Year:  2005        PMID: 16211503     DOI: 10.1007/s10969-005-1909-6

Source DB:  PubMed          Journal:  J Struct Funct Genomics        ISSN: 1345-711X


  30 in total

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6.  Process-scale disruption of microorganisms.

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Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-02-25

8.  Ligation-independent cloning of PCR products (LIC-PCR).

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9.  Using nondenaturing mass spectrometry to detect fortuitous ligands in orphan nuclear receptors.

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Review 10.  Mycobacterium tuberculosis: a model system for structural genomics.

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  3 in total

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2.  MARINE-EXPRESS: taking advantage of high throughput cloning and expression strategies for the post-genomic analysis of marine organisms.

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3.  Towards a comprehensive structural coverage of completed genomes: a structural genomics viewpoint.

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  3 in total

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