Thisproposaldescribesaconcertedapproachtothedesign,synthesis,andstudyofanovelreactiveself- assembly approach, templated by proteins. In this approach, the templating proteins are incarcerated as guests into a matrix of host polymers. The resultant nanoassemblies are programmed to release these encapsulatedproteinsintheirpristineforminthepresenceofaspecificbiologically-relevantstimulusordue to a combination of such stimuli. A key goal of the proposed research is to develop this into a new supramolecularplatformthatisusefulforabroadrangeofsolubleproteins,acapabilitythatdoesnotcurrently exist.Theprimarypremiseoftheproposedresearchthenistodevelopafundamentalframeworkforcustom- designing such supramolecular assemblies that can predictably encapsulate a protein, protect it from denaturationinnon-nativeenvironments,andregainitsnativestructureandfunctioninresponsetoastimulus that is specific to the target environment. We will identify the structural factors that underlie the formation of theseprogrammablemolecularassemblies.Wewilldevelopthisapproachandevaluateitsversatilitythrough: (i)elucidationofthefactorsthatcontroltheself-assemblyprocesssuchthattheapproachbecomesbroadly applicable to a wide-range of proteins;? (ii) incorporate responsive features in the assemblies for a range of specific intrinsic biological triggers, as well as specific combinations of such triggers;? and (iii) evaluation of strategiestotrafficproteinsacrossacellularmembranetoreleasetheminspecificintracellularcompartments. The proposed research will result inanovel, polymeric supramolecular platform with implications in several unmetchallengesinbiomedicine.

Public Health Relevance

Thispremiseofthisprojectistodevelopthefundamentalunderstandingofthestructuralfactorsthatunderlie the formation of supramolecular assemblies, formed due to the reactive self-assembly of polymers and proteins. These molecular assemblies are programmable, in that these can be triggered to disassemble in thepresenceofabiologicallyrelevantstimulusoracombinationsuchstimuli.Suchprogrammedassemblies haveutilityinabroadrangeofunmetbiomedicalapplications.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM128181-01A1
Application #
9659517
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Fabian, Miles
Project Start
2019-02-01
Project End
2022-11-30
Budget Start
2019-02-01
Budget End
2019-11-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Massachusetts Amherst
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
153926712
City
Hadley
State
MA
Country
United States
Zip Code
01035