Peptide mapping analysis by combining the enzymatic digestion and the MALDI-TOF-MS has emerged as a powerful tool for identification and characterization of protein. We describe a nanoliter microreactor prepared with immobilization of enzyme on the porous wall of a capillary. The advantages of the prepared micro-reactor for digestion of the proteins are the elimination of enzyme autolysis and concentration of the micro-sample. Horse heart cytochrome c is selected as the target protein for the evaluation of micro-reactor, and it is found that about 0.1 picomole of protein analyte could routinely be digested for peptide mapping analysis and even femtomole of protein can be well characterized
Thesis (Ph. D.)--University of Washington, 2006.Capillary electrophoresis-mass spectrometry (CE-MS) ...
A miniaturized on-column digestion system constructed for the sequential analysis of semi-purified p...
The following report details the development of novel methods for characterizing proteins. In one ca...
A nanoliter trypsin-based monolithic microreactor coupled with mu RPLC-MS/MS was reported for shotgu...
In the present paper, the covalent immobilisation of the digesting enzyme trypsin has been achieved ...
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been combined with immo...
Peptide mass mapping analysis, utilizing a regenerable enzyme microreactor with metal-ion chelated a...
Protein identification through peptide mass mapping by matrix-assisted laser desorption/ionization t...
Recently, microfluidic systems have been paid much attention to achieve high throughput proteome ana...
In this work we evaluated a novel microreactor prepared using a surface modified, high surface-to-vo...
In this work we evaluated a novel microreactor prepared using a surface modified, high surface-to-vo...
The ultimate goal of proteomics is to study biological processes comprehensively by the systematic a...
A novel monolithic enzymatic microreactor was prepared in the fused-silica capillary by in situ poly...
A monolithic enzymatic microreactor was prepared in a fused-silica capillary by in situ polymerizati...
Digestion is an indispensable step for protein analysis with bottom-up strategy. However, the tradit...
Thesis (Ph. D.)--University of Washington, 2006.Capillary electrophoresis-mass spectrometry (CE-MS) ...
A miniaturized on-column digestion system constructed for the sequential analysis of semi-purified p...
The following report details the development of novel methods for characterizing proteins. In one ca...
A nanoliter trypsin-based monolithic microreactor coupled with mu RPLC-MS/MS was reported for shotgu...
In the present paper, the covalent immobilisation of the digesting enzyme trypsin has been achieved ...
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been combined with immo...
Peptide mass mapping analysis, utilizing a regenerable enzyme microreactor with metal-ion chelated a...
Protein identification through peptide mass mapping by matrix-assisted laser desorption/ionization t...
Recently, microfluidic systems have been paid much attention to achieve high throughput proteome ana...
In this work we evaluated a novel microreactor prepared using a surface modified, high surface-to-vo...
In this work we evaluated a novel microreactor prepared using a surface modified, high surface-to-vo...
The ultimate goal of proteomics is to study biological processes comprehensively by the systematic a...
A novel monolithic enzymatic microreactor was prepared in the fused-silica capillary by in situ poly...
A monolithic enzymatic microreactor was prepared in a fused-silica capillary by in situ polymerizati...
Digestion is an indispensable step for protein analysis with bottom-up strategy. However, the tradit...
Thesis (Ph. D.)--University of Washington, 2006.Capillary electrophoresis-mass spectrometry (CE-MS) ...
A miniaturized on-column digestion system constructed for the sequential analysis of semi-purified p...
The following report details the development of novel methods for characterizing proteins. In one ca...