Ultra High Sensitivity Proteomic Profiling of Limited Samples

Numerous fields of biomedical research could benefit from the availability of highly sensitive methods to define specific phenotypic, physiological or activation states in microscopic amounts of various biological or clinical specimens by measuring enormously complex and highly dynamic molecular interplays in the proteome.

Thus, technology development to advance the current state-of-the-art proteomic profiling techniques to reach the desired levels of sensitivity is of great importance for solving multiple challenging problems in fundamental and clinical research. We laid the groundwork for advancing the sensitivity of the mass spectrometry based techniques and ultimately for enabling single cell proteomic profiling by developing both ultra-low flow rate pressure- and electric field-driven high performance separation techniques. We have also developed ultra-narrow bore monolithic and porous layer open tubular (PLOT) columns to reach unprecedentedly low detection limits (low zeptomoles) in mass spectrometry-based proteomic profiling.

A. Advanced sample preparation for limited samples

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Schejbal J., et al.

Li S., et al. Mol Cell Proteomics, 2015

Kostas J., et al.

B. Ultra-low flow LC-MS-based proteomic profiling of limited samples

Li S., et al. Mol Cell Proteomics, 2015

 

Greguš M., et al.

 

Greguš M., et al.

Greguš M., et al.

Greguš M., et al.

Greguš M., et al.

D. Ultra-low flow CE-MS-based glycomic profiling of limited samples

Marie A.-L., et al.

Marie A.-L., et al.

CONTACT US 

Office Location

140 The Fenway, Room 416TF (Mailstop 412TF)

Northeastern University,

Barnett Institute of Chemical and Biological Analysis,

360 Huntington Avenue, 412TF

Boston, MA, 02115, USA

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