Liam successfully defended his dissertation “Boundary lipids of nicotinic acetylcholine receptors in model and native membranes” in front of his committee, CCIB, and many enthusiastic family members today. He did a fantastic job. We wish him luck at his new postdoc in the lab of Dr. Edward Lyman at the University of Delaware. The lab won’t be the same without you, Liam!
After a successful Fall 2021 rotation cycle, the lab has two new members! We are very excited to welcome Jahmal Ennis and Connor Pitman, who are both graduate students in Computational and Integrative Biology
Jesse Sandberg won the best poster award (MS section) at the 2020 CCIB retreat for his poster “Novel Membrane Bending Mechanism of the Coronavirus Envelope (E) Protein.” The E protein of the coronavirus plays a very important role in shape of the viral envelope, but we don’t know why! Jesse’s poster explored a potential explanation revealed by simulation. Great work!
The group was very well-represented at this year’s CCIB Best Student Paper Contest. Ruchi tied for first place with her paper Sequence specificity despite intrinsic disorder: How a disease-associated Val/Met polymorphism rearranges tertiary interactions in a long disordered protein and Liam was awarded third place for his paper Boundary lipids of the nicotinic acetylcholine receptor: Spontaneous partitioning via coarse-grained molecular dynamics simulation. Ruchi and Liam competed against a record number of entries this year, and this is well-deserved recognition for two great papers. Congratulations!
Collaborative work with the Hill lab at University of Basel was just published in Structure! “The Structural Basis for Low Conductance in the Membrane Protein VDAC upon β-NADH Binding and Voltage Gating” used NMR, electrophysiology, and atomistic MD simulations to study the mitochondrial ion channel VDAC. VDAC is a beta-barrel protein with a much larger and less-sensitive pore than the ligand-gated ion channels we also study. For channels with very narrow pores, understanding how conduction starts can be tricky, but for VDAC it is harder to understand why conduction ever stops. Sruthi and Shashank contributed atomistic MD simulations of NMR structures solved by the Hill lab.
Jesse Sandberg, an MS student in the Graduate Program in Computational and Integrative Biology, is joining the group. Jesse will be using free energy calculations to predict whether small molecules like insecticides, antibiotics, and candidate drugs will block human GABA(A) receptors, causing neurotoxicity. Welcome, Jesse!
Collaborative work with the Cheng lab at Washington University-St Louis was just published in eLife! “Direct binding of phosphatidylglycerol at specific sites modulates desensitization of a ligand-gated ion channel” used electrophysiology, mass spectrometry, and coarse-grained simulations. The work demonstrates quantitatively that the prokaryotic pentameric-ligand gated ion channel ELIC sorts membrane lipids to increase the number of charged-lipid headgroups (particularly phosphatidylglycerol headgroups) in its vicinity. Liam contributed coarse-grained MD simulations of ELIC in multiple lipid mixtures, with results that corresponded remarkably well to the experimental data.
Collaborative work with the Baenziger and Ulens labs was just published in Nat Chem Bio! “A lipid site shapes the agonist response of a pentameric ligand-gated ion channel” investigates the role of specifically-bound lipids in gating a neurotransmitter receptor. Kristen contributed atomistic simulations of structures from the Ulens lab.
Ruchi’s paper “Sequence Specificity Despite Intrinsic Disorder : How a Disease-Associated Val/Met Polymorphism Rearranges Tertiary Interactions in a Long Disordered Protein” was just published in PLOS Computational Biology! This paper focuses on a common variation in Brain-derived Neurotrophic Factor (BDNF). About 70% of the US population has two copies of the “V” form of the protein, 25% has one copy of the “V” form and one copy of the “M” form, and 5% has two copies of the “M” form. The particular copies you have can affect how you store memories and respond to stress.
The region of the protein containing the variant is disordered, and normally we would expect the “V” and “M” forms to behave very similarly. It was unclear why this small change would make any difference at all. In this paper we found that although the two forms do interact similarly with water, the “M” form (on the right) introduces a specific “Met-Met” interaction. We often don’t consider Met-Met interactions, even though they are common in structured proteins. Here we showed that they can also affect the behavior of disordered proteins, which in turn contributes to the natural variation among human brains.
Ruchi successfully defended her PhD thesis “Predicting the effect of genetic variance on the sequence-ensemble relationship of intrinsically disordered proteins.” Ruchi’s thesis used techniques ranging from sophisticated simulations requiring millions of supercomputing hours, to bioinformatics surveys of thousands of proteins.
During her thesis, Ruchi produced thousands of plots, diagrams, and figures in an effort to understand why a seemingly subtle change can have substantial effects. Then she did much harder work: left most of these figures on her hard-drive, and selected a compelling few that revealed a very cool scientific story. Congratulations, Ruchi!