Single Molecule In Vivo Analysis of Toll-Like Receptor 9 and CpG DNA Interaction

Jiji Chen, Birck Nanotechnology Center, Purdue University
Suman Nag, Tata Institute of Fundamental Research
Pierre-Alexandre Vidi, Purdue University
Joseph Irudayaraj, Birck Nanotechnology Center, Purdue University

Date of this Version

4-4-2011

Citation

Chen J, Nag S, Vidi P-A, Irudayaraj J (2011) Single Molecule In Vivo Analysis of Toll-Like Receptor 9 and CpG DNA Interaction. PLoS ONE 6(4): e17991. doi:10.1371/journal.pone.0017991

Comments

Chen J, Nag S, Vidi P-A, Irudayaraj J (2011) Single Molecule In Vivo Analysis of Toll-Like Receptor 9 and CpG DNA Interaction. PLoS ONE 6(4): e17991. doi:10.1371/journal.pone.0017991

The following article has been submitted to/accepted by PLOS ONE. Copyright (2011) Jiji Chen, Suman Nag, Pierre-Alexandre Vidi, Joseph Irudayaraj. This article is distributed under a Creative Commons Attribution License 4.0 .

Abstract

Toll-like receptor 9 (TLR9) activates the innate immune system in response to oligonucleotides rich in CpG whereas DNA lacking CpG could inhibit its activation. However, the mechanism of how TLR9 interacts with nucleic acid and becomes activated in live cells is not well understood. Here, we report on the successful implementation of single molecule tools, constituting fluorescence correlation/cross-correlation spectroscopy (FCS and FCCS) and photon count histogram (PCH) with fluorescence lifetime imaging (FLIM) to study the interaction of TLR9-GFP with Cy5 labeled oligonucleotide containing CpG or lacking CpG in live HEK 293 cells. Our findings show that i) TLR9 predominantly forms homodimers (80%) before binding to a ligand and further addition of CpG or non CpG DNA does not necessarily increase the proportion of TLR9 dimers, ii) CpG DNA has a lower dissociation constant (62 nM +/- 9 nM) compared to non CpG DNA (153 nM +/- 26 nM) upon binding to TLR9, suggesting that a motif specific binding affinity of TLR9 could be an important factor in instituting a conformational change-dependant activation, and iii) both CpG and non CpG DNA binds to TLR9 with a 1: 2 stoichiometry in vivo. Collectively, through our findings we establish an in vivo model of TLR9 binding and activation by CpG DNA using single molecule fluorescence techniques for single cell studies.

Discipline(s)

Nanoscience and Nanotechnology

 

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