Mass Spectrometry Breaks New Ground in Proteomics, Metabolomics and Diagnostics

June 2, 2017
Mass Spectrometry Breaks New Ground in Proteomics, Metabolomics and Diagnostics
Source: Waters Corporation

Chris Anderson, Editor in Chief

There is nothing uncommon about finding a mass spectrometer (MS) in the research labs of academia and pharmaceutical companies, or even in the clinical labs of major hospitals and academic medical centers. For decades it has been a valuable tool in these settings for the detection of small molecules and for immunosuppressant monitoring, along with its prominent role in pharmacokinetic studies in drug clinical trials.

But today, due to significant improvements in the sensitivity and specificity of mass spec instruments, along with more powerful bioinformatics, the technology is playing an increasingly important role in the detection and analysis of metabolites and proteins that serve as biomarkers for a range of diseases (see page 28).


“Our ability to map out the proteomic landscape within tumor tissue has steadily grown over the past two decades,” said Iain Mylchreest, Ph.D., vice president, R&D analytical instruments, Thermo Fisher Scientific. “Advances in mass spectrometry and informatics now allow us to study protein samples on an unprecedented scale with increased depth of analysis both qualitatively and quantitatively.”


These improvements in MS technologies have helped spur researchers working in a number of different areas including infectious diseases, automimmune diseases, and cancer, among others.


“With the introduction of the orbitrap family of instruments, where you are getting both high sensitivity and high resolution, you can do both identification and verification with a simple instrument for PRM experiments,” said Vathany Kulasingam, Ph.D., a clinical biochemist at University Health Network, Toronto, whose work focuses on identifying protein biomarkers in ovarian cancer. “That has helped to almost revolutionize the way we approach our pipeline.


“When we first started in the mid 2000s, we used the LTQ ring ion traps and we could identify 200, 300, 400 proteins, and we were really excited about that,” continued Dr. Kulasingam. “But now a typical run will identify 5,000 to 7,000 proteins. So the depth of analysis has increased, and it is not just data-dependent acquisitions, but also quantification on the same instrument.”

 

Hurdles for Broader MS Adoption


While many larger academic medical centers may be using MS on a regular basis, its broader adoption in the diagnostics labs of health systems and larger hospitals may yet rely of future developments, Mylchreest noted.
“Healthcare testing labs may be reluctant to adapt this technology based on high cost of initial investment, perceived complexity and the talent (specialized resources) required to develop and validate protocols,” he said.

 

Click here to access the rest of this article.

×

Oops! Please type your email in the following format: [email protected]

You’re all set!
Thank you for subscribing to
Clinical OMICs Weekly
.