Our group's research is in the area of analytical mass spectrometry (MS).
The major objectives of the research are to develop advanced methods and
strategies, primarily based on MS, for the detection and characterization
of biological molecules, including peptides, proteins, and metabolites, and to
apply these methods to study real-world biological systems. The latter is
being accomplished through active collaboration with researchers at the
forefront of their disciplines.
Our group is particularly interested in the analysis of biosystems, such as
organelles, cells, tissues, and body fluids, by an interdisciplinary research
approach that uses advanced analytical technologies and sophisticated
bioinformatics tools to produce, interrelate, and integrate a large body of
chemical and biological information on a biological system. Unlike
medicine and systems biology, where more emphasis is on an overall
understanding of the functions in a biological system, biosystems analysis
focuses on the process of data generation and integration. Thus it can be
considered as an important and fundamental part of systems biology and medicine.
Biosystems analysis requires analytical technologies having high sensitivity,
specificity, and throughput to identify and quantify the chemical constituents
of biosystems. Of the many available technologies, mass spectrometry is
playing an increasingly important role in detection, identification and
characterization of biological molecules. One major focus of our research is
to develop enabling mass spectrometric tools for comprehensive proteome
(the set of proteins that is or can be expressed by an organism) and
metabolome (the set of all metabolites found in an organism, cell, or tissue)
analysis.
Biosystems analysis is important in many areas of bioscience and
biomedical research. For example, information on changes to the genome
(the set of all genes in an organism), proteome, and metabolome of cells
grown under different conditions (e.g., normal cell vs. diseased cell) can
help us to understand better the biological functions of individual cellular
components, which, in turn, can assist us to search for drug targets and drug
candidates for better treatment and management of a disease. In the area of
biomarker discovery, large-scale and systematic profiling of proteins and
metabolites in biological samples, such as blood gathered from healthy and
diseased populations, could result in the discovery of a number of chemicals
that could potentially be used for early diagnosis and prognosis of a disease
such as cancer.
Our current research activities include the following major projects:
Development of analytical methods based on matrix-assisted laser
desorption ionization (MALDI) and electrospray ionization (ESI) MS
for proteome and metabolome analysis. The goals of this work are:
1) to generate accurate and comprehensive proteome and metabolome
maps; 2) rapid quantification of proteome and metabolome changes;
and 3) to carry out in-depth analysis of a sub-proteome, such as
characterization of protein posttranslational modifications.
Development of nanoscale biological macromolecule manipulation
and preparation methods for MS. The aim of this work is to improve
mass spectrometric detection sensitivity and specificity for
characterizing low abundance proteins and analyzing very small
amounts of samples, such as a single cell or primary cells procured
from a tissue.
Development and applications of proteomic and metabolomic
approaches in cancer biology, cancer biomarker discovery, and
pharmaceutical drug development.
Development of mass spectrometric techniques for rapid and accurate identification of bacteria.
Additional research projects related to the Proteomics Initiative funded by the Alberta Cancer Board can be found in the Bronco (Bioinformatics Resource for Oncology) web site at www.bronco.ualberta.ca.