ProjectAbstract Biological networks organize specific chemical reactions in space and time. In cell signaling, scaffold proteins coordinate the formation of physical complexes that link multiple signaling proteinstogether.Thesescaffoldproteinshavemanyfunctionalroles:theycanrecruitproteinsto particular subcellular locations, serve as platforms to recruit regulatory factors, and direct pathwaystospecificoutputs.Scaffoldproteinsarealsothoughttoacceleratespecificbiochemical reactionswhenenzymesandproteinsarebroughttogethertothesamespatiallocation.Similar spatial organizing principles are involved in genome regulation, where the 3D structure of the genomeappearstoplayaregulatoryfunctionbypositioninggenesinproximitytoremoteDNA regulatorysitesortolocalizedproteins.Again,physicalproximityisthoughttopromotespecific biochemical processes in gene regulation. While there is extensive evidence that spatial organizationisimportantforbiologicalfunction,welackaquantitativeframeworktounderstand howenzymeactivitiesandotherbiochemicalfunctionsareaffectedbyspatialorganization.This gapinourknowledgemustbeaddressedtounderstandfundamentalprocesseslikecellsignaling andgeneregulation,andtointervenetherapeuticallywhentheseprocessesaremisregulated.To address this challenge, I propose to develop new tools to systematically perturb structural organization both in cell signaling networks and in the genome. I plan to use these tools to understand the underlying mechanistic principles that enable cells to control biochemical reactionswithincrediblespatialandtemporalprecision.

Public Health Relevance

Biologicalnetworksareoftenspatiallyorganizedtoensurethatreactionsoccurattherightplace and time inside cells, particularly in fundamental processes like cell signaling and genome organization. We will develop tools to systematically perturb the relative spatial positions of biomolecules involved in these reaction networks, and to assess the functional consequences. Thisapproachwillenableustounderstandunderlyingregulatoryprinciplesandhowtointervene whentheseprocessesaremisregulatedinhumandiseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
3R35GM124773-02S1
Application #
9700898
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Barski, Oleg
Project Start
2017-08-10
Project End
2022-07-31
Budget Start
2018-08-01
Budget End
2019-07-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Washington
Department
Chemistry
Type
Graduate Schools
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195