Nina Miolane, UCSB (firstname.lastname@example.org).
Cornelius Gati, USC (email@example.com).
Applications will be accepted until the position is filled. However, we recommend applying before October 1st, 2021 in order to be given full consideration. Start date is flexible, from November 1st, 2021, for a duration of 3 years. Primary location is UC Santa Barbara, California, USA.
While the development of cryo-electron microscopy (cryo-EM) has already proven to revolutionize the field of structural biology by imaging biomolecules in solution, the vast majority of proteins cannot be reconstructed at a satisfying resolution. Among them, membrane proteins still remain an immense imaging challenge for biologists -- see simulated model in Figure 1 (A). Their inherent flexibility, as well as limited contrast arising from the micelle surrounding the hydrophobic transmembrane domains, make them a difficult object to image. Meanwhile, membrane proteins are prominent targets for over 50% of prescription drugs on the pharmaceutical market, including drugs targeting the treatment of neurological disorders and cancers1. In this context, the technological limitations of cryo-EM imaging restricts our understanding of the proteins’ 3D conformations, and consequently, our knowledge of the associated therapeutic mechanisms - see reconstruction in Figure 1 (B). Improving membrane proteins’ 3D shapes resolution is crucial for medical and pharmacological applications, and timely given the accelerated constructions of cryo-EM facilities around the world and the associated explosion in cryo-EM data - see Figure 1 (C).
Figure 1: (A) Overall model of the metabotropic GABA-B receptor, a membrane protein that is the target for the treatment of muscle spasms, and alcohol addiction. (B) Principal Component Analysis of raw data, displays poor resolution of the reconstructed shapes between the active and inactive states of the protein (Image courtesy of Prof. Gati). (C) Explosion of cryo-EM data at SLAC National Laboratory (Image courtesy of Dr. Yee-Ting Li). (D) Representative cryo-EM “micrograph” images GABA-B membrane proteins, shown circled in green.
The focus of this project is to develop a novel mathematical and statistical method that enhances the resolution of cryo-EM reconstructions, particularly targeting membrane proteins. The successful candidate will revisit the paradigm of 3D biomolecular shape reconstruction from raw 2D cryo-EM -- see Figure 1 (D). To achieve this goal, the successful candidate will use tools for unsupervised deep learning, such as (variational) autoencoders and/or generative adversarial networks -- see Figure 2.
Figure 2: Example of auto-encoder architecture . The input cryoEM image y is encoded into a pose phi by the encoder. The decoder outputs the tomographic projection of the biomolecular structure oriented at phi, and then corrupted by the microscope’s contrast transfer function (CTF).
These tools will be combined with an implementation of the geometry of shape spaces. Such an approach will allow accurate and robust disentanglement of shape, motion and imaging parameters, a challenging requirement for accessing untapped territories of membrane protein imaging.
The successful candidate will be primarily located in Santa Barbara, California, USA. The successful candidate will be part of an international team of collaborators, working with Nina Miolane (Electrical and Computer Engineering, UCSB, Santa Barbara), Cornelius Gati (Structural Biology, USC, Los Angeles), Khanh Dao Duc (Mathematics, University of British Columbia, Vancouver, Canada), Frédéric Poitevin (Biological Imaging, Stanford SLAC, Palo Alto) and Claire Donnat (Statistics, University of Chicago, Chicago). Related travel expenses will be provided and the candidate will have the opportunity to work with Masters and PhD students of the respective teams.
We seek candidates whose research interests are related to deep learning, geometry, and 3D shape analysis and with the following qualifications:
Former experience and contributions within the fields of unsupervised deep learning for cryo-EM image analysis will be a plus.
Interested applicants are invited to send a detailed CV, 2 reference contacts, links to their 5 most significant contributions and to answer a few questions, by filling the form at this link:
We are committed to equity, diversity, and inclusion. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, or national origin, disability status, protected veteran status, or any other characteristic protected by law.
Figure 3: Artist depiction: Membrane proteins captured in four different conformations. Image credits:
Bridge Institute at the USC Michelson Center for Convergent Bioscience.
|Titel||Postdoctoral Fellowship Geometry & Deep Learning for 3D Biological Shape Reconstructions: Reveal Membrane Proteins with Cryo-Electron Microscopy|
|Employer||University of California|
|Job location||Santa Barbara, Santa Barbara|
|Publiceret||august 24, 2021|
|Stillingstyper||Post doc  |
|Områder||Informatik,   Statistik,   Neurologi,   Biomedicinsk teknik,   Bioinformatik,   Strukturbiologi,   Molekylærbiologi,   Medicinsk billeddannelse,   Kunstig intelligens,    and 16 more. Kunstigt neuralt netværk,   Databehandling i matematik, naturvidenskab, teknik og medicin,   Parallel databehandling,   Softwareudvikling,   Datateknik,   Anvendt matematik,   Farmaci og farmakologi,   Geometri og topologi,   Beregningsbiologi,   Computervidenskab,   Beregningsmatematik,   Big Data,   Machine Learning,   Computer Vision,   Signalbehandling,   Billedbehandling  |