A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2021; you can also visit <a rel="external noopener" href="https://minerva-access.unimelb.edu.au/bitstream/handle/11343/263485/PMC3439251.pdf;jsessionid=9E7B666A806160E1AEDF085D386C62B6?sequence=1">the original URL</a>. The file type is <code>application/pdf</code>.
<i title="Springer Nature">
<a target="_blank" rel="noopener" href="https://fatcat.wiki/container/xua5vbjwszdirewaoqnikiu5zm" style="color: black;">BMC Systems Biology</a>
The half-life of a protein is regulated by a range of system properties, including the abundance of components of the degradative machinery and protein modifiers. It is also influenced by protein-specific properties, such as a protein's structural make-up and interaction partners. New experimental techniques coupled with powerful data integration methods now enable us to not only investigate what features govern protein stability in general, but also to build models that identify what<span class="external-identifiers"> <a target="_blank" rel="external noopener noreferrer" href="https://doi.org/10.1186/1752-0509-6-60">doi:10.1186/1752-0509-6-60</a> <a target="_blank" rel="external noopener" href="https://www.ncbi.nlm.nih.gov/pubmed/22682214">pmid:22682214</a> <a target="_blank" rel="external noopener" href="https://pubmed.ncbi.nlm.nih.gov/PMC3439251/">pmcid:PMC3439251</a> <a target="_blank" rel="external noopener" href="https://fatcat.wiki/release/yu24rkudtjgdzgavrei4glokzi">fatcat:yu24rkudtjgdzgavrei4glokzi</a> </span>
more »... determine each protein's metabolic stability. Results: In this work we present five groups of features useful for predicting protein stability: (1) post-translational modifications, (2) domain types, (3) structural disorder, (4) the identity of a protein's N-terminal residue and (5) amino acid sequence. We incorporate these features into a predictive model with promising accuracy. At a 20% false positive rate, the model exhibits an 80% true positive rate, outperforming the only previously proposed stability predictor. We also investigate the impact of N-terminal protein tagging as used to generate the data set, in particular the impact it may have on the measurements for secreted and transmembrane proteins; we train and test our model on a subset of the data with those proteins removed, and show that the model sustains high accuracy. Finally, we estimate system-wide metabolic stability by surveying the whole human proteome. Conclusions: We describe a variety of protein features that are significantly over-or under-represented in stable and unstable proteins, including phosphorylation, acetylation and destabilizing N-terminal residues. Bayesian networks are ideal for combining these features into a predictive model with superior accuracy and transparency compared to the only other proposed stability predictor. Furthermore, our stability predictions of the human proteome will find application in the analysis of functionally related proteins, shedding new light on regulation by protein synthesis and degradation. Australia Full list of author information is available at the end of the article and colleagues'  extensive data set which measures the metabolic stability of about 8000 human proteins. We use this data set to (a) identify the underlying properties that appear to influence protein half-life, (b) develop a predictive model that integrates a number of different relevant data sets and is able to explain its predictions, (c) chart the metabolic stability of the full human proteome in silico, and therefore (d) infer what features influence stability on a global scale. High-throughput methods for measuring protein degradation typically involve either metabolic labeling or
<a target="_blank" rel="noopener" href="https://web.archive.org/web/20210717221909/https://minerva-access.unimelb.edu.au/bitstream/handle/11343/263485/PMC3439251.pdf;jsessionid=9E7B666A806160E1AEDF085D386C62B6?sequence=1" title="fulltext PDF download" data-goatcounter-click="serp-fulltext" data-goatcounter-title="serp-fulltext"> <button class="ui simple right pointing dropdown compact black labeled icon button serp-button"> <i class="icon ia-icon"></i> Web Archive [PDF] <div class="menu fulltext-thumbnail"> <img src="https://blobs.fatcat.wiki/thumbnail/pdf/16/87/16877bbc18471ddaea9a594b45064c273a004821.180px.jpg" alt="fulltext thumbnail" loading="lazy"> </div> </button> </a> <a target="_blank" rel="external noopener noreferrer" href="https://doi.org/10.1186/1752-0509-6-60"> <button class="ui left aligned compact blue labeled icon button serp-button"> <i class="unlock alternate icon" style="background-color: #fb971f;"></i> springer.com </button> </a> <a target="_blank" rel="external noopener" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439251" title="pubmed link"> <button class="ui compact blue labeled icon button serp-button"> <i class="file alternate outline icon"></i> pubmed.gov </button> </a>