Difference between revisions of "Alzforum / Protein Ontology Kick-Off Meeting"

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'''Date and Venue'''
+
The Alzforum / Protein Ontology collaboration is a driving biological project of the NIGMS-funded [http://pir.georgetown.edu/pro/ Protein Ontology] initiative.
  
October 4-5, Buffalo, NY
+
==Goals of the meeting==
 +
 
 +
The goal of this meeting is to initiate a project to create a protein information resource that will address the needs of Alzheimer's Disease (AD) researchers in a maximally effective way. The focus of the meeting will be directed primarily towards identifying these needs through discussion with specialists in different aspects of AD research. The intended long-term outcome will take the form of  elaborations and extensions of the Protein Ontology (PRO), of new applications of the ontology to annotation of AD research results, and of new PRO-based software tools to support AD research.
  
==Goals of the meeting==
+
==Date and Venue==
  
The goal of this meeting is to initiate a project to create a protein information resource that will address the needs of Alzheimers Disease (AD) researchers in a maximally effective way.  
+
October 4-5, 2011, [http://www.hotelbuffaloamherst.com/ Hotel Indigo], Buffalo, NY
  
The project forms part of the NIGMS-funded Protein Ontology initiative. Topics to be addressed at the meeting will include
+
==Topics to be addressed==
  
 
'''Protein Variants'''
 
'''Protein Variants'''
 +
 
How can we most effectively represent information pertaining to the variants associated with AD and to the relations between them; for example, what level of specificity of descriptions of variants would best address the requirements of AD researchers? In the case of APP, for example, what are the genetic variants of relevance to APP? How should the Protein Ontology deal with such variants in order to assist researchers?
 
How can we most effectively represent information pertaining to the variants associated with AD and to the relations between them; for example, what level of specificity of descriptions of variants would best address the requirements of AD researchers? In the case of APP, for example, what are the genetic variants of relevance to APP? How should the Protein Ontology deal with such variants in order to assist researchers?
  
 
'''Aggregates of proteins / Protein complexes'''
 
'''Aggregates of proteins / Protein complexes'''
 +
 
What are the different kinds of aggregates and complexes relevant to AD, how do AD researchers treat them?   
 
What are the different kinds of aggregates and complexes relevant to AD, how do AD researchers treat them?   
  
Line 28: Line 32:
 
2. Protein complex case study: In addition to the issues addressed above as these arise for protein complexes, this case study will address in addition: criteria for being a complex - what amount of stability is necessary, component stoichiometry and structure, modifications/changes to complexes and associated functional changes.
 
2. Protein complex case study: In addition to the issues addressed above as these arise for protein complexes, this case study will address in addition: criteria for being a complex - what amount of stability is necessary, component stoichiometry and structure, modifications/changes to complexes and associated functional changes.
  
==Very Tentative Schedule==
+
==Schedule==
 +
 
 +
'''Monday, October 3'''
 +
 
 +
From 7:00pm Dinner / Informal Reception, Blue Fire Restaurant, Marriott Hotel (next door to Indigo Hotel)
  
 
'''Tuesday, October 4'''
 
'''Tuesday, October 4'''
 +
 +
8:30am Continental Breakfast
  
 
9:30am
 
9:30am
 +
Moderator: Darren Natale
 +
*Alan Ruttenberg: Introduction to the Project
 +
*Dominic Walsh: [http://ontology.buffalo.edu/pro/Walsh.ppt Introduction to Alzheimer's Disease Research]
 +
*Barry Smith: [http://ontology.buffalo.edu/pro/smith.ppt Introduction to Ontology for Biomedical Scientists]
 +
*Cathy Wu: [http://ontology.buffalo.edu/pro/Wu.pdf Introduction to the Protein Ontology]
  
*Introduction to the project; introduction of project personnel
+
10:30am Refreshment Break
*Introduction to the AD research problems to be addressed
 
*Introduction to ontology for scientists
 
  
10:30am Break
+
11:00am
 +
*Elizabeth Wu: [http://ontology.buffalo.edu/pro/EWu.pdf The Alzforum]
  
11:00am
+
12:30pm Lunch
  
*Short tutorial on the Protein Ontology and associated web tools (including feedback)
+
1:30pm
*Review of proteomics information tools, resources used by AD researchers, unmet needs
+
Moderator: Barry Smith
 +
*Cecilia Arighi: [http://pir.georgetown.edu/~arighic/temp/PROAlzforum_Arighi_10_2011.pptx Short Tutorial] on the PRO Website and Associated Tools
  
12:30pm Lunch
+
3:00pm Refreshment Break
  
1:30pm AD-relevant variants, complexes, aggregates
+
3:30
 +
Moderator: Darren Natale
 +
*Michael Wolfe: [http://ontology.buffalo.edu/pro/Wolfe.ppt The Amyloid Hypothesis of Alzheimer Pathogenesis]
 +
*Tim Danford: [http://ontology.buffalo.edu/pro/Danford.pptx On Using Exons to Define Isoforms]
  
6:00pm Dinner
+
6:00pm Dinner: 270 Campbell Blvd, Getzville, NY 14068.
  
 
'''Wednesday, October 5'''
 
'''Wednesday, October 5'''
  
9:00am Case Studies
+
8:30am Continental Breakfast
 +
 
 +
9:00am  
 +
Moderator: Cathy Wu
 +
Review of Existing Coverage of AD-Related Proteins
 +
 
 +
*Peter d'Eustachio: [http://ontology.buffalo.edu/pro/Reactome.pptx Reactome]
 +
 
 +
*Darren Natale: [http://ontology.buffalo.edu/pro/Natale_PRO-Coverage.ppt PRO Coverage of AD-Related Proteins]
 +
 
 +
*Fahim Imam: [http://ontology.buffalo.edu/pro/imam.pptx Neuroscience Information Framework (NIF) and the Neurodegenerative Disease Phenotype Ontology]
 +
 
 +
*Paolo Ciccarese: Annotation of Neuroscientific Data
 +
::[http://hypothesis.alzforum.org/swan/browser/showEntity!showHypothesisRGraph1.action?objectId=urn%3Alsid%3Aswan.org%3Aresearchstatement%3Abbdc006c-b5ee-412e-b539-ce73fb69c171 AlzSwan Example]
 +
 
 +
10:30am Refreshment Break
 +
 
 +
11:00am *Alex Diehl: [http://ontology.buffalo.edu/pro/Diehl.pptx Neurological Disease Ontology]
 +
 
 +
11:45 Discussion of sample research questions
 +
 
 +
*Find all Creb1 isoform(s) expresssed in the brain by cell type and the antibodies that can be used to detect them
 +
*What is the relationship of obesity and type I and II diabetes to AD?
 +
*What is the expression of AD-related genes in obesity and diabetes?
 +
*What is the effect of insulin on pathology, clinical manifestations and neuroimaging in AD?
 +
*What is the effect of insulin in expression of AD-related genes?
 +
*What is APP695?
 +
*What are the recorded phosphorylation sites in human APP?
 +
*What are the recorded substrates of gamma secretase in human cells?
 +
*What proteins interact with APP?
 +
*What are the transcriptional targets of AICD?
 +
*Which antibodies target the C terminus of human APP?
 +
*Which cleavage products of APP are secreted?
 +
*What forms of Abeta have been found in human brain (vs. in cell culture,  mouse brain, etc.)?
 +
*How does Abeta affect mitochondria?
 +
*Which kinases phosphorylate Tau at threonine 181?
 +
*What are the defined domains in human APP? How do these domains compare to those in mouse?
 +
*What Abeta peptides longer than 43 amino acids (starting at Asp-1) are found in amyloid plaques?
 +
*Wild type 3RTau found as predominant species of Tau in neurofibrillar tangles in certain disease states.
  
 
12:30pm Lunch
 
12:30pm Lunch
  
 
1:30pm Case Studies
 
1:30pm Case Studies
 +
*Expert review of PRO definitions
 +
 +
[http://pir.georgetown.edu/cgi-bin/pro/browser_pro?ids=PR:000010173 Tau]
 +
 +
[http://pir.georgetown.edu/cgi-bin/pro/browser_pro?ids=PR:000004168#O Amyloid beta]
 +
 +
Potential additional topics for discussion
 +
*Animal Models
 +
*[http://www.genome.jp/kegg/pathway/hsa/hsa05010.html Alzheimer's Disease according to KEGG]
  
 
2:30pm Project planning
 
2:30pm Project planning
 +
*Three possible uses for a resource like PRO in a field such as AD research:
 +
::To enable more powerful computation in information-driven research
 +
::To aid non-experts in a given field to access information in that field
 +
::To aid experts in the field find new information, identify new hypothesis, or perform virtual testing of existing hypotheses 
  
3:30pm Main meeting ends
+
*Delineating the biological systems relevant to AD
 +
 
 +
3:30pm Main meeting ends / Refreshment Break
  
 
Technical session for selected participants during rest of day.
 
Technical session for selected participants during rest of day.
 +
*Coordination of Alzforum and PRO Curation
 +
 +
6:00pm Dinner
  
==Intending Participants==
+
==Participants==
*Cecilia Arighi (University of Delaware)
+
*Cecilia Arighi (PRO / University of Delaware)
*Peter d'Eustachio (NYU School of Medicine, New York)
+
*Paolo Ciccarese (Massachusetts General Hospital / Harvard Medical School, Boston)
*Alex Diehl (University at Buffalo)
+
*Alexander Cox (University at Buffalo)
*Darren Natale (Georgetown University Medical Center, Washington DC)
+
*Kelly Anne Dakin (Alzforum, Boston)
 +
*Paresh Dandona (University at Buffalo)
 +
*Timothy Danford (Novartis, Boston)
 +
*Peter D'Eustachio (Reactome / NYU School of Medicine, New York)
 +
*Alexander Diehl (CL, GO / University at Buffalo)
 +
*Fahim Imam (NIF / University of California at San Diego)
 +
*Mark Jensen (University at Buffalo)
 +
*Darren Natale (PRO / Georgetown University Medical Center, Washington DC)
 +
*Mark Ressler (University at Buffalo)
 +
*Caryn-Amy Rose (Alzforum, Boston)
 
*Alan Ruttenberg (University at Buffalo)
 
*Alan Ruttenberg (University at Buffalo)
 
*Barry Smith (University at Buffalo)
 
*Barry Smith (University at Buffalo)
 
*Kinga Szigati (University at Buffalo)  
 
*Kinga Szigati (University at Buffalo)  
*Michael Wolfe (Harvard Medical School, Boston)
+
*Dominic M. Walsh (Brigham & Women's Hospital, Harvard Institutes of Medicine, Boston)
*Cathy Wu (University of Delaware)
+
*Michael Wolfe (Brigham & Women's Hospital, Center for Neurologic Diseases, Boston)
 +
*Cathy Wu (PRO / University of Delaware)
 
*Elizabeth Wu (Alzforum, Boston)
 
*Elizabeth Wu (Alzforum, Boston)

Latest revision as of 12:41, 5 October 2011

The Alzforum / Protein Ontology collaboration is a driving biological project of the NIGMS-funded Protein Ontology initiative.

Goals of the meeting

The goal of this meeting is to initiate a project to create a protein information resource that will address the needs of Alzheimer's Disease (AD) researchers in a maximally effective way. The focus of the meeting will be directed primarily towards identifying these needs through discussion with specialists in different aspects of AD research. The intended long-term outcome will take the form of elaborations and extensions of the Protein Ontology (PRO), of new applications of the ontology to annotation of AD research results, and of new PRO-based software tools to support AD research.

Date and Venue

October 4-5, 2011, Hotel Indigo, Buffalo, NY

Topics to be addressed

Protein Variants

How can we most effectively represent information pertaining to the variants associated with AD and to the relations between them; for example, what level of specificity of descriptions of variants would best address the requirements of AD researchers? In the case of APP, for example, what are the genetic variants of relevance to APP? How should the Protein Ontology deal with such variants in order to assist researchers?

Aggregates of proteins / Protein complexes

What are the different kinds of aggregates and complexes relevant to AD, how do AD researchers treat them?

We envisage two case studies in the course of the meeting, both of which will be designed to serve as guidance for Protein Ontology developers in the initial phases of the project:

1. Protein case study: Perform a detailed review of one class of proteins important to AD research, chosen to be part of the research agenda of at least one of the AD scientists, to bring all participants up to the same level of understanding about what is known. Issues to be addressed will include:

importance of recording non-protein constituents
multimerism
relations to disease hypotheses
kinds of evidence
research plan
protein knowledge queries that would aid the AD researchers
protein knowledge queries that would help others retrieve AD research results

2. Protein complex case study: In addition to the issues addressed above as these arise for protein complexes, this case study will address in addition: criteria for being a complex - what amount of stability is necessary, component stoichiometry and structure, modifications/changes to complexes and associated functional changes.

Schedule

Monday, October 3

From 7:00pm Dinner / Informal Reception, Blue Fire Restaurant, Marriott Hotel (next door to Indigo Hotel)

Tuesday, October 4

8:30am Continental Breakfast

9:30am Moderator: Darren Natale

10:30am Refreshment Break

11:00am

12:30pm Lunch

1:30pm Moderator: Barry Smith

  • Cecilia Arighi: Short Tutorial on the PRO Website and Associated Tools

3:00pm Refreshment Break

3:30 Moderator: Darren Natale

6:00pm Dinner: 270 Campbell Blvd, Getzville, NY 14068.

Wednesday, October 5

8:30am Continental Breakfast

9:00am Moderator: Cathy Wu Review of Existing Coverage of AD-Related Proteins

  • Paolo Ciccarese: Annotation of Neuroscientific Data
AlzSwan Example

10:30am Refreshment Break

11:00am *Alex Diehl: Neurological Disease Ontology

11:45 Discussion of sample research questions

  • Find all Creb1 isoform(s) expresssed in the brain by cell type and the antibodies that can be used to detect them
  • What is the relationship of obesity and type I and II diabetes to AD?
  • What is the expression of AD-related genes in obesity and diabetes?
  • What is the effect of insulin on pathology, clinical manifestations and neuroimaging in AD?
  • What is the effect of insulin in expression of AD-related genes?
  • What is APP695?
  • What are the recorded phosphorylation sites in human APP?
  • What are the recorded substrates of gamma secretase in human cells?
  • What proteins interact with APP?
  • What are the transcriptional targets of AICD?
  • Which antibodies target the C terminus of human APP?
  • Which cleavage products of APP are secreted?
  • What forms of Abeta have been found in human brain (vs. in cell culture, mouse brain, etc.)?
  • How does Abeta affect mitochondria?
  • Which kinases phosphorylate Tau at threonine 181?
  • What are the defined domains in human APP? How do these domains compare to those in mouse?
  • What Abeta peptides longer than 43 amino acids (starting at Asp-1) are found in amyloid plaques?
  • Wild type 3RTau found as predominant species of Tau in neurofibrillar tangles in certain disease states.

12:30pm Lunch

1:30pm Case Studies

  • Expert review of PRO definitions

Tau

Amyloid beta

Potential additional topics for discussion

2:30pm Project planning

  • Three possible uses for a resource like PRO in a field such as AD research:
To enable more powerful computation in information-driven research
To aid non-experts in a given field to access information in that field
To aid experts in the field find new information, identify new hypothesis, or perform virtual testing of existing hypotheses
  • Delineating the biological systems relevant to AD

3:30pm Main meeting ends / Refreshment Break

Technical session for selected participants during rest of day.

  • Coordination of Alzforum and PRO Curation

6:00pm Dinner

Participants

  • Cecilia Arighi (PRO / University of Delaware)
  • Paolo Ciccarese (Massachusetts General Hospital / Harvard Medical School, Boston)
  • Alexander Cox (University at Buffalo)
  • Kelly Anne Dakin (Alzforum, Boston)
  • Paresh Dandona (University at Buffalo)
  • Timothy Danford (Novartis, Boston)
  • Peter D'Eustachio (Reactome / NYU School of Medicine, New York)
  • Alexander Diehl (CL, GO / University at Buffalo)
  • Fahim Imam (NIF / University of California at San Diego)
  • Mark Jensen (University at Buffalo)
  • Darren Natale (PRO / Georgetown University Medical Center, Washington DC)
  • Mark Ressler (University at Buffalo)
  • Caryn-Amy Rose (Alzforum, Boston)
  • Alan Ruttenberg (University at Buffalo)
  • Barry Smith (University at Buffalo)
  • Kinga Szigati (University at Buffalo)
  • Dominic M. Walsh (Brigham & Women's Hospital, Harvard Institutes of Medicine, Boston)
  • Michael Wolfe (Brigham & Women's Hospital, Center for Neurologic Diseases, Boston)
  • Cathy Wu (PRO / University of Delaware)
  • Elizabeth Wu (Alzforum, Boston)