Literature DB >> 19915800

A microscale protein NMR sample screening pipeline.

Paolo Rossi1, G V T Swapna, Yuanpeng J Huang, James M Aramini, Clemens Anklin, Kenith Conover, Keith Hamilton, Rong Xiao, Thomas B Acton, Asli Ertekin, John K Everett, Gaetano T Montelione.   

Abstract

As part of efforts to develop improved methods for NMR protein sample preparation and structure determination, the Northeast Structural Genomics Consortium (NESG) has implemented an NMR screening pipeline for protein target selection, construct optimization, and buffer optimization, incorporating efficient microscale NMR screening of proteins using a micro-cryoprobe. The process is feasible because the newest generation probe requires only small amounts of protein, typically 30-200 microg in 8-35 microl volume. Extensive automation has been made possible by the combination of database tools, mechanization of key process steps, and the use of a micro-cryoprobe that gives excellent data while requiring little optimization and manual setup. In this perspective, we describe the overall process used by the NESG for screening NMR samples as part of a sample optimization process, assessing optimal construct design and solution conditions, as well as for determining protein rotational correlation times in order to assess protein oligomerization states. Database infrastructure has been developed to allow for flexible implementation of new screening protocols and harvesting of the resulting output. The NESG micro NMR screening pipeline has also been used for detergent screening of membrane proteins. Descriptions of the individual steps in the NESG NMR sample design, production, and screening pipeline are presented in the format of a standard operating procedure.

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Year:  2009        PMID: 19915800      PMCID: PMC2797623          DOI: 10.1007/s10858-009-9386-z

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  36 in total

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5.  Effective rotational correlation times of proteins from NMR relaxation interference.

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  52 in total

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5.  A topical issue: production and labeling of biological macromolecules for NMR investigations.

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Review 6.  Advances in protein NMR provided by the NIGMS Protein Structure Initiative: impact on drug discovery.

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7.  Structure and dynamics of Helicobacter pylori nickel-chaperone HypA: an integrated approach using NMR spectroscopy, functional assays and computational tools.

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8.  Solution NMR structure of CGL2373, a polyketide cyclase-like protein from Corynebacterium glutamicum.

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9.  A New Method for Determining Structure Ensemble: Application to a RNA Binding Di-Domain Protein.

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10.  The dynamics of interleukin-8 and its interaction with human CXC receptor I peptide.

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