We propose to develop a robust method to encapsulate biological macromolecules inside porous nano-scale (30-100 nm diameter) phospholipid vesicles. The pores will be formed by Staphylococcal toxin alpha-hemolysin. These ultrasmall, biocompatible containers will allow the passage of small molecules such as ATP and magnesium ions, while limiting the diffusional motion of macromolecules inside the zeptoliter volume, thereby enabling new types of biophysical analysis at the single-molecule level. While the method keeps the molecules essentially free of surface artifacts, the vesicles can be tethered to a supported bilayer so that single molecule reactions can be observed for seconds or even minutes. Therefore, this technique has the potential of transforming the way single-molecule fluorescence measurements are performed in many laboratories around the world. We will also pursue light-activatable pores so that biochemical reactions can be triggered locally, which should enable high-throughput, high time resolution single molecule analysis. If the time scale of pore activation is fast, this approach could also prove useful in ensemble kinetic studies since it has a number of advantages over stopped flow methods or conventional uncaging methods. We will use well-characterized systems such as the hairpin ribozyme and the Holliday junction to probe the pore formation process. Furthermore we will use these techniques to make new biological discoveries on the activities of RNA enzymes and helicases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21GM074526-03
Application #
7228913
Study Section
Special Emphasis Panel (ZRG1-BPC-R (50))
Program Officer
Lewis, Catherine D
Project Start
2005-05-01
Project End
2009-04-30
Budget Start
2007-05-01
Budget End
2009-04-30
Support Year
3
Fiscal Year
2007
Total Cost
$158,737
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Physics
Type
Schools of Engineering
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Lai, Ying; Diao, Jiajie; Liu, Yanxin et al. (2013) Fusion pore formation and expansion induced by Ca2+ and synaptotagmin 1. Proc Natl Acad Sci U S A 110:1333-8
Diao, Jiajie; Ishitsuka, Yuji; Lee, Hanki et al. (2012) A single vesicle-vesicle fusion assay for in vitro studies of SNAREs and accessory proteins. Nat Protoc 7:921-34
Cisse, Ibrahim I; Kim, Hajin; Ha, Taekjip (2012) A rule of seven in Watson-Crick base-pairing of mismatched sequences. Nat Struct Mol Biol 19:623-7
Diao, Jiajie; Ishitsuka, Yuji; Bae, Woo-Ri (2011) Single-molecule FRET study of SNARE-mediated membrane fusion. Biosci Rep 31:457-63
Diao, Jiajie; Su, Zengliu; Lu, Xiaobing et al. (2010) Single-Vesicle Fusion Assay Reveals Munc18-1 Binding to the SNARE Core Is Sufficient for Stimulating Membrane Fusion. ACS Chem Neurosci 1:168-174
Ishitsuka, Yuji; Okumus, Burak; Arslan, Sinan et al. (2010) Temperature-independent porous nanocontainers for single-molecule fluorescence studies. Anal Chem 82:9694-701
Diao, Jiajie; Su, Zengliu; Ishitsuka, Yuji et al. (2010) A single-vesicle content mixing assay for SNARE-mediated membrane fusion. Nat Commun 1:54
Okumus, Burak; Arslan, Sinan; Fengler, Stephanus M et al. (2009) Single molecule nanocontainers made porous using a bacterial toxin. J Am Chem Soc 131:14844-9
Joo, Chirlmin; Balci, Hamza; Ishitsuka, Yuji et al. (2008) Advances in single-molecule fluorescence methods for molecular biology. Annu Rev Biochem 77:51-76
Su, Zengliu; Ishitsuka, Yuji; Ha, Taekjip et al. (2008) The SNARE complex from yeast is partially unstructured on the membrane. Structure 16:1138-46

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