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1.
Electrophoresis ; 31(3): 440-7, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20119951

ABSTRACT

To facilitate a direct interface between protein separation by PAGE and protein identification by mass spectrometry, we developed a multichannel system that continuously collects fractions as protein bands migrate off the bottom of gel electrophoresis columns. The device was constructed using several short linear gel columns, each of a different percent acrylamide, to achieve a separation power similar to that of a long gradient gel. A "Counter Free-Flow" elution technique then allows continuous and simultaneous fraction collection from multiple channels at low cost. We demonstrate that rapid, high-resolution separation of a complex protein mixture can be achieved on this system using SDS-PAGE. In a 2.5 h electrophoresis run, for example, each sample was separated and eluted into 48-96 fractions over a mass range of approximately 10-150 kDa; sample recovery rates were 50% or higher; each channel was loaded with up to 0.3 mg of protein in 0.4 mL; and a purified band was eluted in two to three fractions (200 microL/fraction). Similar results were obtained when running native gel electrophoresis, but protein aggregation limited the loading capacity to about 50 microg per channel and reduced resolution.


Subject(s)
Electrophoresis, Polyacrylamide Gel/instrumentation , High-Throughput Screening Assays , Proteins/isolation & purification , Bacterial Proteins/chemistry , Bacterial Proteins/isolation & purification , Desulfovibrio vulgaris/chemistry , Electrophoresis, Polyacrylamide Gel/methods , Mass Spectrometry , Molecular Weight , Proteins/chemistry , Time Factors
2.
Anal Chem ; 80(19): 7639-42, 2008 Oct 01.
Article in English | MEDLINE | ID: mdl-18763810

ABSTRACT

We describe a contact printing approach for microarrays that uses fused-silica capillary tubes with tapered tips for printing pins and a pressure/vacuum system to control pin loading, printing, and cleaning. The printing process is insensitive to variable environmental factors such as humidity, and the small diameter of the pins allows routine printing from 1536 well source plates. Pin load capacity, 0.2 microL in the current system, is adjustable by controlling pin length. More than 2000 spots can be printed per 0.2-microL pin load (<100 pl/spot), and densities of >12,000 spots/cm(2) are readily achievable. Solutions with a wide range of viscosities and chemical properties can be printed. The system can print tens of thousands of different solutions at high speed, due to the ability to use large numbers of pins simultaneously, and can produce a large number of replicate arrays since all of the solution picked up by the pins is available for deposition.


Subject(s)
Microarray Analysis/instrumentation , Silicon Dioxide/chemistry , Chromosomes, Artificial, Bacterial/chemistry , Chromosomes, Artificial, Bacterial/genetics , DNA/genetics , DNA/isolation & purification , Humans , Microarray Analysis/methods , Oligonucleotide Array Sequence Analysis/instrumentation , Oligonucleotide Array Sequence Analysis/methods , Oligonucleotides/chemistry , Oligonucleotides/genetics , Vacuum
3.
J Struct Biol ; 149(1): 17-29, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15629654

ABSTRACT

A film-handling machine (robot) has been built which can, in conjunction with a commercially available film densitometer, exchange and digitize over 300 electron micrographs per day. Implementation of robotic film handling effectively eliminates the delay and tedium associated with digitizing images when data are initially recorded on photographic film. The modulation transfer function (MTF) of the commercially available densitometer is significantly worse than that of a high-end, scientific microdensitometer. Nevertheless, its signal-to-noise ratio (S/N) is quite excellent, allowing substantial restoration of the output to "near-to-perfect" performance. Due to the large area of the standard electron microscope film that can be digitized by the commercial densitometer (up to 10,000 x 13,680 pixels with an appropriately coded holder), automated film digitization offers a fast and inexpensive alternative to high-end CCD cameras as a means of acquiring large amounts of image data in electron microscopy.


Subject(s)
Densitometry/methods , Automation , Densitometry/instrumentation , Equipment Design , Image Processing, Computer-Assisted , Photography , Robotics , Software
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