Literature DB >> 19499003

High-throughput sample preparation for protein or peptide structural characterization.

D G Sheer1, A M Pitt.   

Abstract

High-performance liquid chromatography (HPLC) combined with mass spectrometry has become the method of choice for identifying and characterizing cell-expressed biomolecules. This technology has evolved so rapidly that efficient sample preparation in a high-throughput mode has become a rate-limiting step. Applications using C18 resin, 200 A pore size, and 15-microm bead size silica and sulfonated divinylbenzene particles were tested. The convenient, solvent-resistant, 96-well MultiScreen filter plates with the Multiscreen Column Loader provided efficient removal of salts and detergents and excellent sample recovery for small volumes. The 96-well simultaneous, uniform loading of dry powders, beads, or resins in 45-, 80-, or 100-microL volumes easily accommodates various media capacities and elution volumes. Recovered eluates demonstrated high well-to-well reproducibility during analyte adsorption, washing, and elution. Sample recovery was analyzed by HPLC for a variety of proteins, peptides, and proteolytic digests. The utility of MultiScreen 96-well mini-columns in performing sample clean-up was also demonstrated for HPLC and mass spectroscopy.

Entities:  

Year:  1999        PMID: 19499003      PMCID: PMC2291579     

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  32 in total

1.  The yeast two-hybrid system: prospects for protein linkage maps.

Authors:  C Evangelista; D Lockshon; S Fields
Journal:  Trends Cell Biol       Date:  1996-05       Impact factor: 20.808

2.  The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs.

Authors:  R J Kaufman; M V Davies; V K Pathak; J W Hershey
Journal:  Mol Cell Biol       Date:  1989-03       Impact factor: 4.272

3.  The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase.

Authors:  K D Wilkinson; K M Lee; S Deshpande; P Duerksen-Hughes; J M Boss; J Pohl
Journal:  Science       Date:  1989-11-03       Impact factor: 47.728

4.  Long-range electrostatic interactions can influence the folding, stability, and cooperativity of dihydrofolate reductase.

Authors:  K M Perry; J J Onuffer; M S Gittelman; L Barmat; C R Matthews
Journal:  Biochemistry       Date:  1989-09-19       Impact factor: 3.162

5.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel; J D Roberts; R A Zakour
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

6.  Site-directed mutagenesis of mouse dihydrofolate reductase. Mutants with increased resistance to methotrexate and trimethoprim.

Authors:  J Thillet; J Absil; S R Stone; R Pictet
Journal:  J Biol Chem       Date:  1988-09-05       Impact factor: 5.157

7.  A novel genetic system to detect protein-protein interactions.

Authors:  S Fields; O Song
Journal:  Nature       Date:  1989-07-20       Impact factor: 49.962

8.  Isolation and expression of an altered mouse dihydrofolate reductase cDNA.

Authors:  C C Simonsen; A D Levinson
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

9.  The structure of mouse L1210 dihydrofolate reductase-drug complexes and the construction of a model of human enzyme.

Authors:  D K Stammers; J N Champness; C R Beddell; J G Dann; E Eliopoulos; A J Geddes; D Ogg; A C North
Journal:  FEBS Lett       Date:  1987-06-22       Impact factor: 4.124

10.  Kinetics of the formation and isomerization of methotrexate complexes of recombinant human dihydrofolate reductase.

Authors:  J R Appleman; N Prendergast; T J Delcamp; J H Freisheim; R L Blakley
Journal:  J Biol Chem       Date:  1988-07-25       Impact factor: 5.157

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