Research is a major part of the mission and day-to-day life of the Department of Chemistry and Biochemistry. Our faculty and students conduct groundbreaking research that has practical applications in everyday life–from the heath care and medications we receive to the energy we use to make our world go, and beyond.  

Our research laboratories are housed in the Life Sciences and Bioengineering Center at Gateway Park, a state-of-the art, major research facility in which bays are organized by research focus rather than by department and researchers from the full range of life science disciplines freely exchange ideas.

Learn about our research interests of faculty members in the WPI Department of Chemistry & Biochemistry:

José M. Argüello

How Heavy Metals Are Escorted into Cells

In his busy lab, José Argüello, professor of chemistry and biochemistry, is studying the biochemical ballet by which cells transport metal micronutrients, such as copper, zinc, cobalt, and iron, across their membranes and to the sites where they play such fundamental roles as helping blood transport oxygen or plants fix nitrogen from the air. Because of the importance of these basic biological functions, a better understanding of the mechanisms of heavy metal transport has implications for the treatment of a host of diseases like tuberculosis, for human and animal nutrition, and for the bioremediation of heavy metal pollution.

He has received multiple research grants from the National Science Foundation (NSF) and the National Institutes of Health (NIH), including an NIH Research Development Award for Minority Faculty in 1995 and a $1.3 million award in 2016 for a systematic study of copper in the bacteria Pseudomonas aeruginosa, a leading cause of hospital-associated infections. He was recently elected Fellow of the American Association for the Advancement of Science (AAAS), the world’s largest general scientific society, “for distinguished research discoveries elucidating the mechanisms underlying metal ion transport and the role of bacterial metal transporters in agriculture and infectious disease.” Research interests include: Mechanisms of micronutrient metal transport in biological systems; membrane protein chemistry; role of micronutrient metals in pathogenic virulence and endocytic symbiosis; role of bacterial metal transport proteins in tuberculosis and in plant nitrogen fixation. Learn more about Professor Argüello

Shawn C. Burdette

Prof. Burdette investigates multidisciplinary research at the interface of metals, biology and photochemistry. Most of the projects in the Burdette group begin with the synthesis of chemical tools that are designed to execute a particular task such as bind and release a metal of interest. The new chemical tools are then characterized spectroscopically and applied to answering a question in a related field like biology either within the group or in collaboration with other groups. Research interests include: Bioorganic zinc chemistry; metals in neurotransmission; metal ion signaling in biology; metal in homeostasis; metal ion chelators: binding and selectivity; organic photochemistry/photochemical tools; small-molecule and polymer-based fluorescent sensors; new fluorophores and chromophores; ligand synthesis; living polymerization methods. Learn more about Professor Burdette.

Robert E. Dempski

Prof. Dempski’s research focuses on understanding the mechanism of biomedically essential, but understudied membrane proteins. This includes the human zinc ZIP4 transporter which has been implicated in the initiation and progression and solid tissue tumors such as pancreatic cancer as well as the light activated channelrhodopsin-2 ion channel, a central tool in the emerging field of optogenetics. Learn more about Professor Dempski. ​

James P. Dittami

The research in Prof. Dittami’s group is directed at the development of new synthetic methods, the synthesis of natural products and the design and synthesis of therapeutically active analogs. Research interests include: Organic synthesis; natural product synthesis; synthetic photochemistry; drug development and drug discovery.  Learn more about Professor Dittami.

Arne Gericke

Prof. Gericke is interested in studying signal transduction pathways and investigating how lipids mediate protein functions – in particular, the PI 3-kinase signaling pathway, which is one of the major pathways involved in the development of cancer. Prof. Scarlata and Prof. Gericke's group uses sophisticated spectroscopic, kinetic and thermodynamic methods to study lipid/protein interaction in cells and model systems.  Research interests include: Membrane biophysics; lipid-mediated protein functions (phosphoinositides, sphingolipids); membrane trafficking; vibrational spectroscopic imaging of tissue. Learn more about Professor Gericke.

Prof. Grimm’s group uses an X-ray Photoelectron Spectrometer to study the properties of novel materials
Prof. Grimm’s group uses an X-ray
Photoelectron Spectrometer to study the
properties of novel materials.

Prof. Grimm is a physical chemist interested in understanding questions like “what makes a particular material efficient at converting sunlight to electrical or chemical energy?” Conversely, what makes a material a poor energy converter? Using a range of spectroscopic techniques, his group seeks an atom- and bond-level understanding of the properties of novel materials.  

Supramolecular chemistry is the design of molecular materials and structures that exhibit useful properties resulting from the collective interaction of different molecular components. The Grimmgroup is motivated by quantifying and controlling the bulk and surface properties of solar energy conversion materials.  Learn more about Professor Grimm.

Dr. Heilman and his lab is working to discover how a virus can destroy only cancerous cells directly with the hope of developing new cancer therapies. He spoke to in a video explaining how viruses function and how the machinery of a virus could be hijacked to cure diseases. Research interests include: Animal virus protein; apoptosis; cancer cell selectivity; subcellular localization; functional domain mutagenesis. Learn more about Professor Heilman

George A. Kaminski

Finding Proteins that Can Attack Disease

Prof. Kaminski is a computational physical chemist who models small molecule/protein interactions. Toxic proteins are at the root of many diseases, so pharmaceutical companies look for compounds called ligands that will bind tightly to these proteins and deactivate them. He has developed powerful new computational tools that will make the search faster and more precise.

The tools use principles of physics to predict protein-ligand binding based on the chemistry and structure of target compounds. Research interests include: Computational chemistry/molecular modeling; protein simulations; force field development; Monte Carlo simulations. Learn more about Professor Kaminski.

Christopher R. Lambert

Antimicrobial surfaces for device implantation; neuroprosthetics for regenerating nerves and enabling devices; passive cell sorting for blood purification; bioreactor development for tissue growth, manufacturing therapeutics, and creating biofuels; organic photovoltaics; acetylcholinesterase inhibition sensing; blood analytes sensing.  Learn more about Professor Lambert.

John C. MacDonald

Prof. MacDonald focuses on understanding molecular interaction and self-assembly in solution and on surfaces in order to control molecular crystallization and assembly of complex multicomponent systems. His group utilizes synthetic, physical-organic, and supramolecular approaches to generate and study 3-D coordination polymers—called metal-organic frameworks, or MOFs—featuring a range of architectures with high internal surface areas and void volumes. These porous MOF solids serve as host materials that actively absorb and store organic guests. Research interests include: Surface chemistry: molecular thin films; materials chemistry: porous solides (environmental remediation); solid-state organic chemistry: crystal engineering, polymorphism, chiral separations. Learn more about Professor MacDonald.

Prof. Mattson is an organic chemist with a strong medicinal chemistry component in her research. Her research is directed at the synthesis of complex molecules that have pharmaceutical value or promise. Her studies looks at the preparation of important synthetic building blocks using new transformations catalyzed by small organic molecules. Of particular interest is the development of reactions catalyzed by organic molecules through non-covalent interactions. Her group applies these new synthetic methods towards the synthesis of naturally occurring bioactive targets.

She was recently was awarded a grant from the National Science Foundation (NSF) entitled "Chiral silanediols in anion-binding catalysis.” Under this grant, Dr. Mattson will design and implement studies related to chiral silanediols in anion-binding catalysis and will oversee two graduate students in the syntheses of chiral silanediols and the development of innovative enantioselective methodologies reliant on silanediol anion-binding catalysis. Dr. Mattson will also oversee mechanistic studies probing the noncovalent interactions of silanediol-catalyzed anion-binding processes. Learn more about Professor Mattson.

Prof. Perez-Olsen studies the maintenance of cell membrane composition in C. Elegans and how the lipidome is affected by age and/or disease state. In addition, she is interested in identifying genes that are important for regulating membrane maintenance under normal and stressed conditions. She uses advanced mass spectrometry to study the lipid composition of cell membranes. Her research aims to understand the linkage between biomembrane maintenance and diseases like cancer.

Suzanne Scarlata’s lab uses advanced fluorescence microscopy techniques to study membrane signaling events involving G-protein coupled receptors. In this case FRET images of PC12 cells over-expressing eCFP-Gqα and eCYP-Phospholipase Cβ1. The high FRET intensity at the membrane (yellow/red color) indicates that Gqα/PLCβ1β dimer formation at the plasma membrane.
Suzanne Scarlata’s lab uses advanced
fluorescence microscopy techniques
to study membrane signaling events
involving G-protein coupled receptors.
FRET images of PC12 cells over-expressing
eCFP-Gqα and eCYP-Phospholipase Cβ1.
The high FRET intensity at the membrane
(yellow/red color) indicates that Gqα/PLCβ1β
dimer formation at the plasma membrane.

Prof. Scarlata’s group explores how cells communicate with the outside world. This communication system can involve a group of proteins called “G-proteins” that can cause cells to move, divide and change structure. Using biophysical methods, the Scarlata group can watch how cells respond to different agents and try to control their responses.

She uses sophisticated spectroscopic, kinetic and thermodynamic methods to study lipid/protein interaction in cells and model systems. Her own research, funded with a $308,000 annual R01 award from the National Institute of General Medical Sciences, focuses on guanine nucleotide-binding proteins’—or G proteins’—role in transmitting signals to various stimuli in the body, particularly in heart muscle cells and neurons.

She is president of the Biophysical Society, with over 9,000 global members. Her goals in the new role include efforts to establish a more stable U.S. research funding system, spreading the word about the biochemical and physical science realm of WPI, and forging more community collaborations with groups like UMass Medical School. Previously, she was the chair of the societies’ Committee for Professional Opportunities for Women. Prof. Scarlata has pioneered the adoption of the society's gender equity policy that made a 'commitment to inclusivity and diversity and not at the expense of scientific excellence'.