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Ruchi’s paper “Sequence Specificity Despite Intrinsic Disorder : How a Disease-Associated Val/Met Polymorphism Shifts Tertiary Interactions in a Long Disordered Protein” is now submitted, and also available on ChemRxiv. This paper focuses on a mutation in the prodomain of Brain-derived Neurotrophic Factor (BDNF), which is associated with a range of stress-related disorders and neurodegeneration. The mutation can have dramatic effects on axon growth, but it’s such a seemingly subtle mutation (one amino acid is mutated to a similar amino acid, in a dynamic and disordered protein containing almost 100 amino acids), it’s surprising there are any detectable effects. The goal of this paper was to figure out the origin of these differences, so that we can improve our ability to predict which mutations of disordered proteins will actually affect protein function.
These simulations were done with atomistic resolution in explicit water, and took over 30 million hours of CPU time generously allocated by the Rutgers Discovery and Informatics Institute on the supercomputer Caliburn. One of the most interesting parts for us: to extract useful information from this large amount of generated data, we had to conceptualize (“see”) the protein in an entirely different way.
The preference of the nicotinic acetylcholine receptor (nachr) for certain lipid environments has been a subject of debate for decades. Liam’s paper “Boundary lipids of the nicotinic acetylcholine receptor: Spontaneous partitioning via coarse-grained molecular dynamics simulation”, which was just accepted at BBA-Biomembranes, uses coarse-grained molecular dynamics to equilibrate the local lipid environment around an nAChR in a ternary membrane mixture. We find a high affinity of omega-3 fatty acids (like those found in fish oil) for the nAChR interface with the membrane. This suggests there could be specific interactions with nAChR that underly the benefits of fish oil for function of the central nervous system.
“A streamlined, general approach for computing ligand binding free energies and its application to GPCR-bound cholesterol” was just accepted to J. Chem Theory and Computation.
Alchemical free energy perturbation is a rigorous but delicate technique the lab uses frequently for measuring ligand binding affinities. This paper has an updated and simplified approach that we’ve developed over many years. This approach even works for non-dilute reference state or a complex, phase-separated bulk!
Is it only useful for these complicated systems? Nope! We first had to simplify many of the “usual” steps to even think about adding this complexity on top – so we’ve made the usual steps more robust, even for a protein in a dilute aqueous solution.
This paper has a lot of different pieces. It might seem like it is a complicated paper to be advertising a simple streamlined approach! We did need to tie multiple viewpoints and frameworks together in the paper and provide one treatment that resolved several inconsistencies. While this was a lot of work for us (and makes for a comprehensive paper), we hope using the approach and interpreting the results will be far less work for you!
New paper on q-bio on calculations of binding affinities using alchemical free energy perturbation (updated May 2018)
[Update to Submission version May 2018: Substantial simplification of the theory/formalism sections for readability, improved incorporation of quadratic mixture model.]
Alchemical free energy perturbation is a rigorous technique the lab uses frequently for measuring ligand binding affinities. This new paper has an updated and simplified approach that we’ve developed over many years – motivated by challenges in measuring and interpreting binding affinities for membrane proteins. This approach even works for non-dilute reference state or a complex, phase-separated bulk! We’ve also included calculation of cholesterol affinities for 3 different GPCRs as a sample application.
Kristen gave an excellent defense of her MS dissertation “Oligomerization of nicotinic acetylcholine receptors in coarse-grained model membranes” and is now continuing on to complete her PhD in the lab.
Sruthi successfully defended her thesis “Mechanisms underlying effects of genetic variance and general anesthetics on pentameric ligand-gated ion channels” to receive the first Brannigan Lab PhD. She set a strong precedent, by tackling technically challenging problems, uncovering unintuitive mechanisms, publishing a number of papers, and producing some very compelling movies in the process. Congratulations, Sruthi – we are all proud!