We have developed a novel system for coupling reverse-phase (RP) and hydrophilic interaction liquid chromatography (HILIC) online in a micro-flow scheme. In this approach, the inherent solvent incompatibility between RP and HILIC is overcome through the use of constant-pressure online solvent mixing, which allows our system to perform efficient separations of both hydrophilic and hydrophobic compounds for mass spectrometry-based proteomics applications. When analyzing the tryptic digests of bovine serum albumin, ribonuclease B, and horseradish peroxidase, we observed near-identical coverage of peptides and glycopeptides when using online RP-HILIC-with only a single sample injection event-as we did from two separate RP and HILIC analyses. Th...
This chapter presents a methodical overview of recent research literature dealing with the character...
We have developed a fully automatable two-dimensional liquid chromatography platform for shotgun pro...
The diversity and complexity of proteins and peptides in biological systems requires powerful liquid...
Improved methods for detailed characterization of complex glycoproteins are required in the growing ...
This dissertation reports the development of novel, fully automatable, online multidimensional liqui...
In proteomics, nanoflow multidimensional chromatography is now the gold standard for the separation ...
Due to the hydrophilic nature of glycans, reverse phase chromatography has not been widely used as a...
Recent progress in top-down proteomics has driven the demand for chromatographic methods compatible ...
In the last decade, the field of proteomics has rapidly progressed with substantial advances in many...
Although reverse-phase liquid chromatography (RP-LC) is a common technique for peptide separation in...
Protein glycosylation is one of the most common and critical post-translational modification, which ...
Monoclonal antibodies (mAb) and related molecules are being developed at a remarkable pace as new th...
Selective enrichment of glycopeptides from complicated biological samples is critical for glycoprote...
Recent progress in top-down proteomics has driven the demand for chromatographic methods compatible ...
Hydrophobic interaction chromatography (HIC) is a robust standard analytical method to purify prote...
This chapter presents a methodical overview of recent research literature dealing with the character...
We have developed a fully automatable two-dimensional liquid chromatography platform for shotgun pro...
The diversity and complexity of proteins and peptides in biological systems requires powerful liquid...
Improved methods for detailed characterization of complex glycoproteins are required in the growing ...
This dissertation reports the development of novel, fully automatable, online multidimensional liqui...
In proteomics, nanoflow multidimensional chromatography is now the gold standard for the separation ...
Due to the hydrophilic nature of glycans, reverse phase chromatography has not been widely used as a...
Recent progress in top-down proteomics has driven the demand for chromatographic methods compatible ...
In the last decade, the field of proteomics has rapidly progressed with substantial advances in many...
Although reverse-phase liquid chromatography (RP-LC) is a common technique for peptide separation in...
Protein glycosylation is one of the most common and critical post-translational modification, which ...
Monoclonal antibodies (mAb) and related molecules are being developed at a remarkable pace as new th...
Selective enrichment of glycopeptides from complicated biological samples is critical for glycoprote...
Recent progress in top-down proteomics has driven the demand for chromatographic methods compatible ...
Hydrophobic interaction chromatography (HIC) is a robust standard analytical method to purify prote...
This chapter presents a methodical overview of recent research literature dealing with the character...
We have developed a fully automatable two-dimensional liquid chromatography platform for shotgun pro...
The diversity and complexity of proteins and peptides in biological systems requires powerful liquid...