Biology subjects

Guo, H.-B.

Publications and source records attributed to Guo, H.-B..

3 recordsLinked to original sources

bioRxiv2023

AlphaFold2 modeling and molecular dynamics simulations of an intrinsically disordered protein

We use AlphaFold2 (AF2) to model the monomer and dimer structures of an intrinsically disordered protein (IDP), Nvjp-1, assisted by molecular dynamics (MD) simulations. We observe relatively rigid dimeric structures of Nvjp-1 when compared with the monomer structures. We suggest that protein conformations from multiple AF2 models and those from MD trajectories exhibit a coherent trend: the conformations of an IDP are deviated from each other and the conformations of a well-folded protein are consistent with each other. We use a residue-residue interaction network (RIN) derived from the contact map which show that the residue-residue interactions in Nvjp-1 are mainly transient; however, those in a well-folded protein are mainly persistent. Despite the variation in 3D shapes, we show that the AF2 models of both disordered and ordered proteins exhibit highly consistent profiles of the pLDDT (predicted local distance difference test) scores. These results indicate a potential protocol to justify the IDPs based on multiple AF2 models and MD simulations. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=106 SRC="FIGDIR/small/551023v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@65c7f1org.highwire.dtl.DTLVardef@29cb87org.highwire.dtl.DTLVardef@1f126d2org.highwire.dtl.DTLVardef@12bb76d_HPS_FORMAT_FIGEXP M_FIG The TOC figure: C_FIG

biophysics↗

bioRxiv2020

Protein-protein interaction probability landscapes for yeast replicative aging

We proposed a novel probability landscape approach to map the systems-level profile changes of gene networks during replicative aging in Saccharomyces cerevisiae. This approach enabled us to apply quasi-potentials, the negative logarithm of the probabilities, to calibrate the elevation of the landscapes with young cells as a reference state. Our approach detected opposite landscape changes based on protein abundances from transcript levels, especially for intra-essential gene interactions. We showed that essential proteins play different roles from hub proteins on the age-dependent landscapes. We verified that hub proteins tend to avoid other hub proteins, but essential proteins are attractive to other essential proteins. Overall, we showed that the probability landscape is promising for inferring network profile change during aging and that the essential hub proteins may play an important role in the uncoupling between protein and transcript levels during replicative aging.

systems biology↗

bioRxiv2020

Association Study based on Topological Constraints of Protein-Protein Interaction Networks

The non-random interaction pattern of a protein-protein interaction network (PIN) is biologically informative but its potentials have not been fully utilized in omics studies. Here, we propose a network-permutation-based association study (NetPAS) method that gauges the observed interactions between two sets of genes based on the comparison between permutation null models and the empirical networks. This enables NetPAS to evaluate relationships, constrained by network topology, between gene sets related to different phenotypes. We demonstrated the utility of NetPAS in 50 well-curated gene sets and comparison of association studies using Z-scores, p-values or overrepresentations. Using NetPAS, a weighted human disease network was generated from the association scores of 19 gene sets from OMIM. We also applied NetPAS in gene sets derived from gene ontology and pathway annotations and showed that NetPAS uncovered functional terms missed by DAVID and other network-based enrichment tools. Overall, we show that NetPAS can take topological constraints of molecular networks into account and offer new perspectives than existing methods.

bioinformatics↗