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Pilla, K. B.

Publications and source records attributed to Pilla, K. B..

3 recordsLinked to original sources

Recognizing amino acid sidechains in a medium resolution cryo-electron density map

Building an accurate atomic structure model of a protein into a cryo-electron microscopy (cryo-EM) map at worse than 3 [A] resolution is difficult. To facilitate this task, we devised a method for assigning the amino acid residue sequence to the backbone fragments traced in an input cryo-EM map (EMSequenceFinder). EMSequenceFinder relies on a Bayesian scoring function for ranking 20 standard amino acid residue types at a given backbone position, based on the fit to a density map, map resolution, and secondary structure propensity. The fit to a density is quantified by a convolutional neural network that was trained on [~]5.56 million amino acid residue densities extracted from cryo-EM maps at 3-10 [A] resolution and corresponding atomic structure models deposited in the Electron Microscopy Data Bank (EMDB). We benchmarked EMSequenceFinder by predicting the sequences of 58,044 distinct L-helix and {beta}-strand fragments, given the fragment backbone coordinates fitted in their density maps. EMSequenceFinder identifies the correct sequence as the best-scoring sequence in 77.8% of these cases. We also assessed EMSequenceFinder on separate datasets of cryo-EM maps at resolutions from 4 to 6 L. The accuracy of EMSequenceFinder (63.5%) was better than that of three tested state-of-the-art methods, including findMysequence (45%), ModelAngelo (27%), and sequence_from_map in Phenix (12.9%). We further illustrate EMSequenceFinder by threading the SARS-CoV-2 NSP2 sequence into eight cryo-EM maps at resolutions from 3.7 to 7.0 [A]. EMSequenceFinder is implemented in our open-source Integrative Modeling Platform (IMP) program. Thus, it is expected to be helpful for integrative structure modeling based on a cryo-EM map and other information, such as models of protein complex components and chemical crosslinks between them. EMSequenceFinder is available as part of our open source IMP distribution at https://integrativemodeling.org/.

biophysics↗

A SARS-CoV-2-Human Protein-Protein Interaction Map Reveals Drug Targets and Potential Drug-Repurposing

An outbreak of the novel coronavirus SARS-CoV-2, the causative agent of COVID-19 respiratory disease, has infected over 290,000 people since the end of 2019, killed over 12,000, and caused worldwide social and economic disruption1,2. There are currently no antiviral drugs with proven efficacy nor are there vaccines for its prevention. Unfortunately, the scientific community has little knowledge of the molecular details of SARS-CoV-2 infection. To illuminate this, we cloned, tagged and expressed 26 of the 29 viral proteins in human cells and identified the human proteins physically associated with each using affinity-purification mass spectrometry (AP-MS), which identified 332 high confidence SARS-CoV-2-human protein-protein interactions (PPIs). Among these, we identify 66 druggable human proteins or host factors targeted by 69 existing FDA-approved drugs, drugs in clinical trials and/or preclinical compounds, that we are currently evaluating for efficacy in live SARS-CoV-2 infection assays. The identification of host dependency factors mediating virus infection may provide key insights into effective molecular targets for developing broadly acting antiviral therapeutics against SARS-CoV-2 and other deadly coronavirus strains.

systems biology↗

Protein Fold Determination by Assembling Extended Super-Secondary Structure Motifs Using Limited NMR Data

The 3D fold determination of proteins by computational algorithms guided by experimental restraints is a reliable and efficient approach. However, the current algorithms struggle with sampling the conformational space and scaling in performance with the increase in the size of the proteins. This paper demonstrates a new data-driven, time-efficient, heuristics algorithm that assembles the 3D structure of a protein from its elemental super-secondary structure motifs (Smotifs) using a limited number of nuclear magnetic resonance (NMR) derived restraints. The DINGO-NOE-RDC algorithm (3D assembly of Individual smotifs to Near-native Geometry as Orchestrated by limited nuclear Overhauser effects (NOE) and residual dipolar couplings (RDC)) leverages on the distance restraints recorded on methyl-methyl (CH3-CH3), methyl-amide (CH3-HN), and amide-amide (HN-HN) NOE contacts, and orientation restraints recorded via RDC on the backbone amide protons, to assemble the targets Smotifs. Two conceptual advancements were made to bootstrap the structure determination from limited NMR restraints; first, expand the basic definition of a Smotif and, second, employ a data driven approach for selection, scoring, ranking and clustering of Smotif assemblies. In contrast to existing methods, the DINGO-NOE-RDC algorithm does not use any force-fields, physical/empirical scoring functions or the targets amino-acid sequence makeup. Additionally, the algorithm employs a universal Smotif library that applies to any target protein and, can generate numerically reproducible results. For a benchmark set of ten different targets with different topologies, ranging from 100-200 residues, the algorithm identified near-native Smotifs in all of them.

biophysics↗