Difference between revisions of "Research"

From Marcotte Lab
Jump to: navigation, search
(Rational identification of genes affecting traits and diseases)
(Proteomics: High-throughput protein expression and interaction profiling)
 
(38 intermediate revisions by 3 users not shown)
Line 3: Line 3:
 
== Bioinformatics of protein function and interactions ==
 
== Bioinformatics of protein function and interactions ==
  
We've discovered a number of features of genomes that allow us to predict functions for proteins that have never been experimentally characterized. Using these techniques and information from over 30 fully sequenced genomes, we were able to calculate the first genome-wide predictions of protein function, finding very preliminary function for over half the 2,500 uncharacterized genes of yeast. Now, with hundreds of genomes in hand, we're extending these techniques, as well as asking fundamental questions about the evolution of protein interactions and the evolution of genomes. [[File:network.jpg||300px|right]]
+
We've discovered a number of features of genomes that allow us to predict functions for proteins that have never been experimentally characterized. Using these techniques and information from over 30 fully sequenced genomes, we were able to calculate some of the first genome-wide predictions of protein function, finding very preliminary function for over half the 2,500 uncharacterized genes of yeast. Now, with thousands of genomes in hand, we're extending these techniques, as well as asking fundamental questions about the evolution of protein interactions and the evolution of genomes. [[File:network.jpg||300px|right]]
  
 
''Some of our recent papers on gene networks and the systematic discovery of gene function include:''<br>
 
''Some of our recent papers on gene networks and the systematic discovery of gene function include:''<br>
 +
{{Paper
 +
|title=RIDDLE: Reflective diffusion and local extension reveal functional associations for unannotated gene sets via proximity in a gene network
 +
|authors=Wang, Hwang, ''et al.''
 +
|journal=Genome Biology
 +
|pubmed=23268829
 +
|volume=13(12)
 +
|page=R125
 +
|link=http://genomebiology.com/2012/13/12/R125/abstract
 +
|pub_year=2012
 +
}}
 +
 +
{{Paper
 +
|title=Predicting genetic modifier loci using functional gene networks
 +
|authors=Lee, Lehner, ''et al.''
 +
|journal=Genome Research
 +
|pub_year=2010
 +
|volume=20
 +
|page=1143-1153
 +
|pubmed=20538624
 +
|pdf=GenomeResearch_GeneticModifiers_2010.pdf
 +
|link=http://dx.doi.org/10.1101/gr.102749.109
 +
}}
 +
 +
{{Paper
 +
|title=Characterising and predicting haploinsufficiency in the human genome
 +
|authors=Huang ''et al.''
 +
|journal=PLoS Genetics
 +
|pub_year=2010
 +
|volume=6(10)
 +
|pdf=PLoSGenetics_Haploinsufficiency_2010.pdf
 +
|link=http://dx.doi.org/10.1371/journal.pgen.1001154
 +
|page=e1001154
 +
|pubmed=20976243
 +
}}
 +
 
{{Paper
 
{{Paper
 
|title=A single gene network accurately predicts phenotypic effects of gene perturbation in ''Caenorhabditis elegans''
 
|title=A single gene network accurately predicts phenotypic effects of gene perturbation in ''Caenorhabditis elegans''
|authors=Lee ''et al.''
+
|authors=Lee, Lehner ''et al.''
 
|journal=Nature Genetics
 
|journal=Nature Genetics
 
|pub_year=2008
 
|pub_year=2008
Line 67: Line 102:
  
  
Link to our large-scale gene networks for yeast, worms, mouse: http://www.functionalnet.org
+
Link to our large-scale gene networks for yeast, worms, mouse, ''Arabidopsis'': http://www.functionalnet.org. An illustration of our ''Arabidopsis'' gene network just won Honorable Mention in the 2010 [http://www.marcottelab.org/paper-pdfs/848.full.pdf ''Science'' Visualization Challenge] & was featured by the [http://www.nytimes.com/slideshow/2011/02/17/science/20110217-visualize-6.html ''New York Times'']
  
 
Link to some of our public bioinformatics resources: http://bioinformatics.icmb.utexas.edu
 
Link to some of our public bioinformatics resources: http://bioinformatics.icmb.utexas.edu
Line 73: Line 108:
 
== Rational identification of genes affecting traits and diseases ==
 
== Rational identification of genes affecting traits and diseases ==
  
Using the gene networks and other computational tools, we've now gained some ability to rationally predict the consequences to an organism of mutating or interrupting a specific gene. This means that by using these tools, we can often select a small set of candidate genes to be implicated in a particular disease or trait. We've now experimentally validated >100 such candidate genes for diverse traits in a wide range of organisms, including yeast, worms, ''Arabidopsis'', ''C. elegans'', frogs, mice, and humans. For example, in yeast we've used network models to discovery a large number of new ribosome biogenesis genes, as well as genes controlling such features as cell size. In animals, e.g. using our worm gene network models, we could successfully identify new genes controlling longevity, as well as genes capable of suppressing the loss of the Retinoblastoma tumor suppressor, thus 'curing' worms of model tumors. In plants, with now ex-postdoc [http://polaris.icmb.utexas.edu/people/il1001/author.htm Insuk Lee] and collaborator [http://carnegiedpb.stanford.edu/rhee-lab Sue Rhee], we could rationally identify new genes regulating root growth, drought resistance, and seedling pigmentation. In vertebrates, working with the [http://www.bio.utexas.edu/faculty/wallingford/ Wallingford] and [http://gene.tamu.edu/faculty_pages/faculty_FinnellR.php Finnell] labs, we've been able to use gene network models to help assign functions to a birth defect gene, as well as to identify entirely new birth defect genes, confirming their roles ''in vivo''. [[File:worm-synmuv.jpg||300px|right]]
+
Using the gene networks and other computational tools, we've now gained some ability to rationally predict the consequences to an organism of mutating or interrupting a specific gene. This means that by using these tools, we can often select a small set of candidate genes to be implicated in a particular disease or trait. We've now experimentally validated >100 such candidate genes for diverse traits in a wide range of organisms, including yeast, worms, ''Arabidopsis'', ''C. elegans'', frogs, mice, and humans. For example, in yeast we've used network models to discover a large number of new ribosome biogenesis genes (collaborating with [http://www.bio.utexas.edu/faculty/ajohnson/index.htm Arlen Johnson]), as well as genes controlling such features as cell size. In animals, e.g. using our worm gene network models developed with collaborators [http://www.crg.es/ben_lehner Ben Lehner] and [http://www.fraserlab.org/ Andy Fraser], we could successfully identify new genes controlling longevity, as well as genes capable of suppressing the loss of the Retinoblastoma tumor suppressor, thus 'curing' worms of model tumors. In ''Arabidopsis'', with now ex-postdoc [http://polaris.icmb.utexas.edu/people/il1001/author.htm Insuk Lee] and collaborator [http://carnegiedpb.stanford.edu/rhee-lab Sue Rhee], we could rationally identify new genes regulating root growth, drought resistance, and seedling pigmentation. In vertebrates, working with the [http://www.bio.utexas.edu/faculty/wallingford/ Wallingford] and [http://gene.tamu.edu/faculty_pages/faculty_FinnellR.php Finnell] labs, we've been able to use gene network models to help assign functions to a birth defect gene, as well as to identify entirely new birth defect genes, confirming their roles ''in vivo''. [[File:worm-synmuv.jpg||300px|right]]  
  
 
''Some of our recent papers on the rational association of genes with traits and diseases:''<br>
 
''Some of our recent papers on the rational association of genes with traits and diseases:''<br>
 +
 
{{Paper
 
{{Paper
|title=Rational Extension of the Ribosome Biogenesis Pathway Using Network-Guided Genetics
+
|title=Coordinated genomic control of ciliogenesis and cell movement by Rfx2
 +
|authors=Chung, Kwon ''et al.''
 +
|journal=eLife
 +
|pubmed=24424412
 +
|pdf=eLife_RFX2_2014.pdf
 +
|volume=3
 +
|page=e01439
 +
|link=http://dx.doi.org/10.7554/eLife.01439
 +
|pub_year=2014
 +
}}
 +
 
 +
{{Paper
 +
|title=Evolutionarily Repurposed Networks Reveal the Well-Known Antifungal Drug Thiabendazole to Be a Novel Vascular Disrupting Agent
 +
|authors=Cha ''et al.''
 +
|journal=PLoS Biology
 +
|pubmed=
 +
|volume=10(8)
 +
|link=http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001379
 +
|pdf=PLoSBiology_TBZ_2012.pdf
 +
|page=e1001379
 +
|pub_year=2012
 +
|comment=[http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001380 Synopsis] [http://www.nytimes.com/2012/08/21/health/research/clues-to-fighting-cancer-are-found-in-the-genes-of-yeast.html NY Times] [http://publications.nigms.nih.gov/multimedia/repurposing-genes-drugs.html NIGMS video]
 +
}}
 +
 
 +
{{Paper
 +
|title=Prioritizing candidate disease genes by network-based boosting of genome-wide association data
 +
|authors=Lee, Blom, ''et al.''
 +
|journal=Genome Research
 +
|pubmed=21536720
 +
|pub_year=2011
 +
|volume=21(7)
 +
|pdf=GenomeResearch_HumanNet_2011.pdf
 +
|page=1109-21
 +
|link=http://dx.doi.org/10.1101/gr.118992.110
 +
}}
 +
 
 +
{{Paper
 +
|title=Systematic discovery of nonobvious human disease models through orthologous phenotypes
 +
|authors=McGary, Park ''et al.''
 +
|journal=Proc Natl Acad Sci U S A
 +
|pub_year=2010
 +
|volume=107(14)
 +
|page=6544-9
 +
|pubmed=20308572
 +
|link=http://www.pnas.org/cgi/doi/10.1073/pnas.0910200107
 +
|comment=Carl Zimmer wrote [http://www.nytimes.com/2010/04/27/science/27gene.html?_r=1 a nice story about this work] for ''The New York Times''.
 +
}}
 +
 
 +
{{Paper
 +
|title=Rational association of genes with traits using a genome-scale gene network for ''Arabidopsis thaliana''
 +
|authors=Lee ''et al.''
 +
|journal=Nature Biotechnology
 +
|pub_year=2010
 +
|volume=28(2)
 +
|page=149-156
 +
|pubmed=20118918
 +
|link=http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.1603.html
 +
|comment=
 +
}}
 +
 
 +
{{Paper
 +
|title=Rational extension of the ribosome biogenesis pathway using network-guided genetics
 
|authors=Li ''et al.''
 
|authors=Li ''et al.''
 
|journal=PLoS Biology
 
|journal=PLoS Biology
 
|pub_year=2009
 
|pub_year=2009
|volume=(in press)
+
|volume=7(10)  
|page=
+
|page=e1000213
 
|pubmed=19806183
 
|pubmed=19806183
 
|link=http://dx.doi.org/10.1371/journal.pbio.1000213
 
|link=http://dx.doi.org/10.1371/journal.pbio.1000213
Line 93: Line 190:
 
|journal=Nature Cell Biology
 
|journal=Nature Cell Biology
 
|pub_year=2009
 
|pub_year=2009
|volume=(in press)
+
|volume=11(10)
|page=
+
|page=1225-32
|pubmed=  
+
|pubmed=19767740
|link=
+
|link=http://dx.doi.org/10.1038/ncb1966
 
|comment=
 
|comment=
 
}}
 
}}
Line 102: Line 199:
 
{{Paper
 
{{Paper
 
|title=A single gene network accurately predicts phenotypic effects of gene perturbation in ''Caenorhabditis elegans''
 
|title=A single gene network accurately predicts phenotypic effects of gene perturbation in ''Caenorhabditis elegans''
|authors=Lee ''et al.''
+
|authors=Lee, Lehner ''et al.''
 
|journal=Nature Genetics
 
|journal=Nature Genetics
 
|pub_year=2008
 
|pub_year=2008
Line 135: Line 232:
 
|comment=
 
|comment=
 
}}
 
}}
 +
[[File:DRBIlogo.jpg||75px|right]]
  
  
Read more about some of our [http://www.bio.utexas.edu/faculty/wallingford/Pages/Research.html#Computation computational approaches to developmental biology]
+
Use our ''phenolog'' method to link genes to traits: http://www.phenologs.org
 +
 
 +
Read more about some of our [http://www.bio.utexas.edu/faculty/wallingford/Pages/Research.html#Computation computational approaches to developmental biology] & the UT [http://www.bio.utexas.edu/faculty/wallingford/drbi/ Developmental and Regenerative Biology Initiative]
  
 
== Proteomics: High-throughput protein expression and interaction profiling ==
 
== Proteomics: High-throughput protein expression and interaction profiling ==
Line 144: Line 244:
  
 
''Recent papers in this area include:''<br>
 
''Recent papers in this area include:''<br>
 +
{{Paper
 +
|title=Panorama of ancient metazoan macromolecular complexes
 +
|authors=Wan, Borgeson ''et al.''
 +
|journal=Nature
 +
|pubmed=26344197
 +
|volume=525
 +
|page=339–344
 +
|link=http://dx.doi.org/10.1038/nature14877
 +
|pdf=Nature_AnimalComplexes_2015.pdf
 +
|pub_year=2015
 +
}}
 +
 +
{{Paper
 +
|title=Molecular deconvolution of the monoclonal antibodies that comprise the polyclonal serum response
 +
|authors=Wine, Boutz, Lavinder ''et al.''
 +
|journal=Proc Natl Acad Sci USA
 +
|pubmed=23382245
 +
|volume=110(8)
 +
|page=2993–2998
 +
|pdf=PNAS_IgGProfiling_2013.pdf
 +
|pub_year=2013
 +
|link=http://www.pnas.org/content/early/2013/02/01/1213737110.abstract 
 +
}}
 +
 +
{{Paper
 +
|title=Census of Human Soluble Protein Complexes
 +
|authors=Havugimana ''et al.''
 +
|journal=Cell
 +
|pubmed=22939629
 +
|volume=150
 +
|page=1068-1081
 +
|link=http://www.cell.com/abstract/S0092-8674%2812%2901006-9
 +
|pdf=Cell_HumanProteinComplexes_2012.pdf
 +
|pub_year=2012
 +
}}
 +
 +
{{Paper
 +
|title=Insights into the regulation of protein abundance from proteomic and transcriptomic analyses 
 +
|authors=Vogel & Marcotte
 +
|journal=Nature Reviews Genetics
 +
|pubmed=22411467
 +
|volume=13
 +
|link=http://dx.doi.org/10.1038/nrg3185
 +
|pdf=NatureReviewsGenetics_ProteinAbundanceRegulation_2012.pdf
 +
|page=227-232
 +
|pub_year=2012
 +
}}
 +
 +
{{Paper
 +
|title=Sequence signatures and mRNA concentration can explain two-thirds of protein abundance variation in a human cell line
 +
|authors=Vogel ''et al.''
 +
|journal=Molecular Systems Biology
 +
|pub_year=2010
 +
|pubmed=20739923
 +
|volume=6
 +
|page=article 400
 +
|pdf=MolecularSystemsBiology_2010_HumanProteomics.pdf
 +
|link=http://www.nature.com/msb/journal/v6/n1/full/msb201059.html
 +
|comment=[http://www.marcottelab.org/paper-pdfs/MolecularSystemsBiology_2010_HumanProteomics_NewsAndViews.pdf News and Views]
 +
}}
 +
 
{{Paper
 
{{Paper
 
|title=Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation
 
|title=Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation
Line 195: Line 356:
  
 
<br>
 
<br>
Link to our MS/MS data repository: http://www.marcottelab.org/MSdata/ [[File:opd-banner-5I.png||300px|right]]
+
Links to our MS/MS data repositories: http://www.marcottelab.org/MSdata/ and http://www.marcottelab.org/index.php/Category:MSdata [[File:opd-banner-5I.png||300px|right]]
  
 
Link to the Open Proteomics Database: http://bioinformatics.icmb.utexas.edu/OPD/  
 
Link to the Open Proteomics Database: http://bioinformatics.icmb.utexas.edu/OPD/  
 +
 +
Link to the APEX Protocol website: http://marcottelab.org/APEX_Protocol/
 +
 +
Link to the APEX software tool: http://pfgrc.jcvi.org/index.php/bioinformatics/apex.html
 +
 +
Link to the MSpresso website: http://www.marcottelab.org/MSpresso/
 +
 +
Link to the MSblender website: http://www.marcottelab.org/index.php/MSblender  MSblender is proving to be a particularly powerful tool for interpreting mass spectrometry proteomics datasets; we've now used it for >5,000 individual datasets.
 
<br>
 
<br>
 
<br>
 
<br>
Line 204: Line 373:
 
<div style="border:solid green;margin:8px;padding:10px;">
 
<div style="border:solid green;margin:8px;padding:10px;">
 
[[File:Xenopus-PV.jpg||100px|left]] <br>
 
[[File:Xenopus-PV.jpg||100px|left]] <br>
'''Read about our [http://www.bio.utexas.edu/faculty/wallingford/Pages/Research.html#GenomeSeq Texas <i>Xenopus</i> genome project] (!)''', a collaboration with the [http://www.bio.utexas.edu/faculty/wallingford/ Wallingford lab] and the [http://gsaf.cssb.utexas.edu/Site/The_Genomic_Sequencing_and_Analysis_Facility_at_UT_Austin_Main_Page.html UT Genomic Sequencing and Analysis Facility], funded by the [http://www.ti3d.utexas.edu/ Texas Institute for Drug and Diagnostic Development]<br>
+
'''Read about our [[Texas Xenopus Genome Project]]''', a collaboration with the [http://www.bio.utexas.edu/faculty/wallingford/ Wallingford lab] and the [https://wikis.utexas.edu/display/GSAF/Home+Page UT Genomic Sequencing and Analysis Facility], funded by the [http://www.ti3d.utexas.edu/ Texas Institute for Drug and Diagnostic Development]<br>
 
<br>
 
<br>
 
<br>
 
<br>
  
 
</div>
 
</div>

Latest revision as of 10:01, 19 January 2016

Our group studies the large-scale organization of proteins, essentially trying to reconstruct the 'wiring diagrams' of cells by learning how all of the proteins encoded by a genome are associated into functional pathways, systems, and networks. We are interested both in discovering the functions of the proteins as well as in learning the underlying organizational principles of the networks. The work is evenly split between computational and experimental approaches, with the latter tending to be high-throughput functional genomics and proteomics approaches for studying thousands of genes/proteins in parallel.

Contents

Bioinformatics of protein function and interactions

We've discovered a number of features of genomes that allow us to predict functions for proteins that have never been experimentally characterized. Using these techniques and information from over 30 fully sequenced genomes, we were able to calculate some of the first genome-wide predictions of protein function, finding very preliminary function for over half the 2,500 uncharacterized genes of yeast. Now, with thousands of genomes in hand, we're extending these techniques, as well as asking fundamental questions about the evolution of protein interactions and the evolution of genomes.
Network.jpg

Some of our recent papers on gene networks and the systematic discovery of gene function include:
Wang, Hwang, et al., RIDDLE: Reflective diffusion and local extension reveal functional associations for unannotated gene sets via proximity in a gene network, Genome Biology, 13(12):R125 (2012) PubMed Link

Lee, Lehner, et al., Predicting genetic modifier loci using functional gene networks, Genome Research, 20:1143-1153 (2010) PubMed Link PDF

Huang et al., Characterising and predicting haploinsufficiency in the human genome, PLoS Genetics, 6(10):e1001154 (2010) PubMed Link PDF

Lee, Lehner et al., A single gene network accurately predicts phenotypic effects of gene perturbation in Caenorhabditis elegans, Nature Genetics, 40(2):181-8 (2008) PubMed Link

Peña-Castillo et al., A critical assessment of Mus musculus gene function prediction using integrated genomic evidence, Genome Biology, 9 Suppl 1:S2 (2008) PubMed Link

Hart et al., A high-accuracy consensus map of yeast protein complexes reveals modular nature of gene essentiality, BMC Bioinformatics, 8:236. (2007) PubMed Link

Lee et al., A probabilistic functional network of yeast genes, Science, 306(5701):1555-8. (2004) PubMed Link

Fraser, Marcotte, A probabilistic view of gene function, Nature Genetics, 36(6):559-64 (2004) PubMed Link


Link to our large-scale gene networks for yeast, worms, mouse, Arabidopsis: http://www.functionalnet.org. An illustration of our Arabidopsis gene network just won Honorable Mention in the 2010 Science Visualization Challenge & was featured by the New York Times

Link to some of our public bioinformatics resources: http://bioinformatics.icmb.utexas.edu

Rational identification of genes affecting traits and diseases

Using the gene networks and other computational tools, we've now gained some ability to rationally predict the consequences to an organism of mutating or interrupting a specific gene. This means that by using these tools, we can often select a small set of candidate genes to be implicated in a particular disease or trait. We've now experimentally validated >100 such candidate genes for diverse traits in a wide range of organisms, including yeast, worms, Arabidopsis, C. elegans, frogs, mice, and humans. For example, in yeast we've used network models to discover a large number of new ribosome biogenesis genes (collaborating with Arlen Johnson), as well as genes controlling such features as cell size. In animals, e.g. using our worm gene network models developed with collaborators Ben Lehner and Andy Fraser, we could successfully identify new genes controlling longevity, as well as genes capable of suppressing the loss of the Retinoblastoma tumor suppressor, thus 'curing' worms of model tumors. In Arabidopsis, with now ex-postdoc Insuk Lee and collaborator Sue Rhee, we could rationally identify new genes regulating root growth, drought resistance, and seedling pigmentation. In vertebrates, working with the Wallingford and Finnell labs, we've been able to use gene network models to help assign functions to a birth defect gene, as well as to identify entirely new birth defect genes, confirming their roles in vivo.
Worm-synmuv.jpg

Some of our recent papers on the rational association of genes with traits and diseases:

Chung, Kwon et al., Coordinated genomic control of ciliogenesis and cell movement by Rfx2, eLife, 3:e01439 (2014) PubMed Link PDF

Cha et al., Evolutionarily Repurposed Networks Reveal the Well-Known Antifungal Drug Thiabendazole to Be a Novel Vascular Disrupting Agent, PLoS Biology, 10(8):e1001379 (2012) PubMed Link PDF Synopsis NY Times NIGMS video

Lee, Blom, et al., Prioritizing candidate disease genes by network-based boosting of genome-wide association data, Genome Research, 21(7):1109-21 (2011) PubMed Link PDF

McGary, Park et al., Systematic discovery of nonobvious human disease models through orthologous phenotypes, Proc Natl Acad Sci U S A, 107(14):6544-9 (2010) PubMed Link Carl Zimmer wrote a nice story about this work for The New York Times.

Lee et al., Rational association of genes with traits using a genome-scale gene network for Arabidopsis thaliana, Nature Biotechnology, 28(2):149-156 (2010) PubMed Link

Li et al., Rational extension of the ribosome biogenesis pathway using network-guided genetics, PLoS Biology, 7(10):e1000213 (2009) PubMed Link

Gray et al., The planar cell polarity effector protein Fuzzy is essential for targeted membrane trafficking, ciliogenesis, and mouse embryonic development, Nature Cell Biology, 11(10):1225-32 (2009) PubMed Link

Lee, Lehner et al., A single gene network accurately predicts phenotypic effects of gene perturbation in Caenorhabditis elegans, Nature Genetics, 40(2):181-8 (2008) PubMed Link

White et al., Bud23 methylates G1575 of 18S rRNA and is required for efficient nuclear export of pre-40S subunits, Mol Cell Biol, 28(10):3151-61 (2008) PubMed Link

McGary et al., Broad network-based predictability of Saccharomyces cerevisiae gene loss-of-function phenotypes, Genome Biology, 8(12):R258. (2007) PubMed Link

DRBIlogo.jpg


Use our phenolog method to link genes to traits: http://www.phenologs.org

Read more about some of our computational approaches to developmental biology & the UT Developmental and Regenerative Biology Initiative

Proteomics: High-throughput protein expression and interaction profiling

From our work and others, it is apparent that proteins in the cell participate in extended protein interaction networks involving thousands of proteins. By defining these networks, we can not only discover the functions of specific proteins based on their connections, but also use these networks as tools to predict the outcome of perturbing the cell. As part of our research efforts in this area, we have been developing high-throughput methods to measure protein abundances in complex biological samples (e.g., by quantitative shotgun proteomics mass spectrometry) and protein localization with cells (e.g., by high-throughput automated fluorescence microcopy, such as of cell microarrays). These sorts of data help us build a catalog of protein, mRNA and metabolite expression from cells grown under many different conditions, forming a quantitative picture of these molecular events inside cells. We expect that data of these sorts will put us on the road to developing predictive, rather than merely descriptive, theories of biology.

Recent papers in this area include:
Wan, Borgeson et al., Panorama of ancient metazoan macromolecular complexes, Nature, 525:339–344 (2015) PubMed Link PDF

Wine, Boutz, Lavinder et al., Molecular deconvolution of the monoclonal antibodies that comprise the polyclonal serum response, Proc Natl Acad Sci USA, 110(8):2993–2998 (2013) PubMed Link PDF

Havugimana et al., Census of Human Soluble Protein Complexes, Cell, 150:1068-1081 (2012) PubMed Link PDF

Vogel & Marcotte, Insights into the regulation of protein abundance from proteomic and transcriptomic analyses, Nature Reviews Genetics, 13:227-232 (2012) PubMed Link PDF

Vogel et al., Sequence signatures and mRNA concentration can explain two-thirds of protein abundance variation in a human cell line, Molecular Systems Biology, 6:article 400 (2010) PubMed Link PDF News and Views

Narayanaswamy et al., Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation, Proc Natl Acad Sci U S A, 106(25):10147-52 (2009) PubMed Link

Vogel, Marcotte, Calculating absolute and relative protein abundance from mass spectrometry-based protein expression data, Nature Protocols, 3(9):1444-51. (2008) PubMed Link Protocol website

Ramani et al., A map of human protein interactions derived from co-expression of human mRNAs and their orthologs, Molecular Systems Biology, 4:180 (2008) PubMed Link

Lu, Vogel, Wong et al., Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation, Nature Biotechnology, 25(1):117-24 (2007) PubMed Link


Links to our MS/MS data repositories: http://www.marcottelab.org/MSdata/ and http://www.marcottelab.org/index.php/Category:MSdata
Opd-banner-5I.png

Link to the Open Proteomics Database: http://bioinformatics.icmb.utexas.edu/OPD/

Link to the APEX Protocol website: http://marcottelab.org/APEX_Protocol/

Link to the APEX software tool: http://pfgrc.jcvi.org/index.php/bioinformatics/apex.html

Link to the MSpresso website: http://www.marcottelab.org/MSpresso/

Link to the MSblender website: http://www.marcottelab.org/index.php/MSblender MSblender is proving to be a particularly powerful tool for interpreting mass spectrometry proteomics datasets; we've now used it for >5,000 individual datasets.

Recent research news