Kenton J. Swartz, Ph.D.
Dr. Swartz received his B.S. in Chemistry and Biology from Eastern Mennonite College in 1986. He received his Ph.D. in Neurobiology from Harvard University in 1993 where he worked with Bruce Bean studying the regulation of voltage-gated calcium channels by G-proteins and protein kinases. He did postdoctoral training with Roderick MacKinnon at Harvard Medical School, where he began isolating and studying toxins that interact with voltage-activated potassium channels.
Dr. Swartz joined NINDS as an Investigator in 1997 to establish a laboratory studying the structure and operational mechanisms of ion channel proteins. He was promoted to Senior Investigator in 2003, received the NIH Directors Award for Scientific Achievement in 2008 and the Kenneth S. Cole Award from the Biophysical Society in 2017. His laboratory is currently using biochemical, molecular biological, biophysical and structural techniques to investigate the structure and functional mechanisms of voltage-activated ion channels, TRP channels and P2X receptor channels.
Tsg-Hui Chang, M.S.
Helena received her B.S. in Biochemistry and Molecular Biology from the University of Maryland Baltimore County in 1994. She went on to graduate studies in Biochemistry and Molecular Biology at George Washington University where she worked on gap junction proteins and received her MS in 1998. Before joining the Swartz laboratory, she worked at NCI, studying protein expression in lung cancer cells.
As the manager for the Swartz laboratory, Helena has played an important role in helping trainees to get their projects working, assisting them with training and troubleshooting, sharing her expertise in cell and molecular biology, and most recently with membrane protein expression and purification. Helena is the backbone of the laboratory, helping to develop and learn new methods and approaches, and deriving a lot of satisfaction from seeing trainees grow and develop their passion for science.
Surbhi Dhingra, Ph.D.
Surbhi Dhingra received her MS degree in microbiology from S.P. Pune University, India in 2013. She completed her PhD in biotechnology from National Centre for Cell Science, India in 2022. For her doctorate research, she worked on understanding the functional mechanisms of the kainate receptors, a subfamily of ionotropic glutamate receptors, under the guidance of Dr. Janesh Kumar.
She has expertise in molecular biology, protein expression and purification from eukaryotic/prokaryotic systems, biochemical stabilization of proteins in solution and their biophysical characterization using various chromatography techniques, surface plasmon resonance, structural studies using cryo-electron microscopy and functional whole-cell patch-clamp recording. Her research interests are to understand the molecular basis of diverse functions carried out by ion channels in cells as well as their modulation by membrane lipids and auxiliary proteins. She has joined the Swartz laboratory as a postdoctoral fellow in 2022 to explore the functional mechanisms of P2X receptor channels, an interesting class of trimeric ion channels that are activated by extracellular ATP. In her spare time, Surbhi enjoys reading fiction, gardening, badminton and exploring new places.
Anabel Fernandez-Mariño, Ph.D.
Ana Fernandez-Mariño received her BS degree from the Universidade de Vigo in Spain in 2008 and her MS degree in 2009 and her PhD degree in 2013, both from the Universitat Pompeu Fabra in Barcelona. As a graduate student Ana gained expertise in using electrophysiological approaches to study calcium-activated potassium channels.
In 2014 she obtained postdoctoral training with Baron Chanda at the University of Wisconsin where she used innovative biophysical approaches to study the Shaker voltage-activated potassium (Kv) channel to understand the structural mechanism by which voltage-sensing domains couple to the pore domain to control opening of the internal gate. Ana joined the Swartz laboratory in 2017 to use both structural and functional approaches to study the mechanism of slow inactivation in the human ‘ether a-go-go’ (hERG) Kv channel, Shaker and Kv1.3 channels. From her work on inactivation in Kv1.3, she developed an interest in using nanobodies to stabilize specific conformations of Kv channels for both structural and mechanistic studies. Ana is currently focused on using our recent structure of the neuronal Kv2.1 channel along with functional approaches to investigate mechanism of inactivation and to study human mutations causing epileptic encephalopathy.
Charlotte Godfrey, B.S.
Charlotte received her B.S. in Psychology from Appalachian State University in 2021, where she obtained research experience in behavioral neuroscience studying environmental processing in rats. She is fascinated by the finely tuned environment of the cellular membrane in excitable cells and by the opportunities this research poses for understanding biological function and dysfunction.
Her work as a postbaccalaureate fellow in the Swartz laboratory is focused on understanding how the TRPM3 channel is activated by various biological stimuli and exploring structural and functional relationships with other TRP channels. Charlotte’s plan is to pursue graduate studies when she finishes her postbaccalaureate fellowship.
Katherine Huffer, A.B.
Graduate Student, NIH/Hopkins Partnership
Kate Huffer received their AB in Neuroscience and Biological Chemistry from Dartmouth College in 2015 and joined the Swartz laboratory as a postbaccalaureate fellow to study the functional properties of transient receptor potential (TRP) channels before matriculating as a graduate student in the NIH-Johns Hopkins Graduate Partnerships Program.
To facilitate further mechanistic investigations of TRP channels, Kate undertook a comprehensive computational analysis of over 100 available TRP channels structures solved over the past decade, enabling the identification of both conserved and unique structural features involved in how TRP channels open in response to different stimuli or select for permeating ions. Kate has been working to interrogate structural and functional relationships within the TRPM subfamily using both patch-clamp electrophysiology and computational techniques and recently began updating their global analysis of TRP channel structures, which will include over 260 structures.
William Khayyo, B.S.
William Khayyo is a recent graduate from Stony Brook University, where they double majored in Applied Mathematics and Biochemistry with a minor in Chemistry. During their undergraduate studies, William conducted electrophysiology research in the Wollmuth group exploring gating regulatory elements in the transmembrane domain of NMDA receptors.
William also interned in the National Institute of Aging during the 2022 Summer Internship Program under the Laboratory of Genetics and Genomics (LGG). Through this opportunity, they worked closely with the Laboratory of Cardiovascular Sciences (LCS) under Edward Lakatta. They helped refine an analysis pipeline that elucidates spatiotemporal relationships in murine cardiac tissue through processing of calcium imaging videos of murine cardiac samples as a model. William is currently a postbaccalaureate fellow engaged in a collaborative effort between the Swartz laboratory in NINDS and Jose Faraldo-Gomez’s laboratory in NHLBI using both structural and computational approaches to investigate the mechanism of slow inactivation in voltage-activated potassium channels.
Maia Moog, B.S., M.S.
Graduate Student, NIH/Karolinska Institute Partnership
Maia is a PhD student in the Karolinska-NIH collaborative PhD program. Her doctoral project, a collaborative effort between Dr. Kenton Swartz at the National Institutes of Health and Dr. Patrik Ernfors at the Karolinska Institute, focuses on a special type of Schwann cell at the dermal-epidermal border in the skin that plays a role in the initiation and propagation of mechanical pain.
Over the course of her studies, she will draw upon the expertise of the two laboratories to characterize the electrophysiological and molecular properties of these Schwann cells to determine which ion channels play roles in detecting and transducing painful stimuli. Before joining the Swartz Laboratory, Maia received her Master’s in Neuroscience from the University of Helsinki, where she conducted her thesis studies with the Baraban Epilepsy Research Lab at UCSF. The lab is home to dozens of zebrafish models for several forms of human genetic epilepsy. As part of her project, Maia conducted forebrain EEG field recordings in larval zebrafish to identify genes associated the catastrophic childhood epilepsy. Outside of the lab, Maia enjoys cycling. She fell in love with the sport when she cycled across America in 2014 and she hopes to one day explore another country (or continent!) by bike.
Intern and summer student
Elisabeth Oskoui is an undergraduate studying biochemistry at Imperial College London. Her interests lie in structural biology, computational chemistry, and ion channel function, particularly the pharmacology of transient receptor potential (TRP) channels.
She joined the Swartz laboratory in 2020 to work on computational modeling of protein-ligand binding for her senior project in high school. Elisabeth worked as a summer student in 2021 on a computational project using Rosetta to investigate TRP channel protein-ligand interactions, and in 2022 on an experimental project studying pocket conservation and computational analysis of TRP channel pocket motifs. Both projects involved leveraging structural information to examine functional characteristics and regulation of TRP channels.
Purushotham Selvakumar, PhD
Xiaofeng Tan, Ph.D.
E-mail: Tan, email@example.com
Xiaofeng Tan obtained his B.S. in Biotechnology from the University of Science and Technology of China in 2009 and his Ph.D. degree in Biochemistry and Molecular Biology from the same university in 2015. In 2015 Xiaofeng moved to the United States to learn X-ray crystallography at the University of California, Riverside, and cryo-electron microscopy in the laboratory of Jiansen Jiang in NHLBI.
In 2020 Xiaofeng joined the Swartz laboratory, where his main interest has been to elucidate key functional mechanisms in voltage-activated potassium (Kv) channels using single particle cryo-EM. Most recently he succeeded in elucidating the long-sought mechanism of slow C-type inactivation in the Shaker Kv channel, revealing that inactivation leads to the unanticipated dilation of the ion selectivity filter within the external pore of the channel. His big dream is to understand the mechanism of voltage sensing and how voltage-sensor activation controls opening and closing of the internal pore of Kv channels.