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Single molecule resolution of the antimicrobial action of quantum dot-labeled sushi peptide on live bacteria

Sebastian Leptihn1* email, Jia Yi Har1* email, Jianzhu Chen1,2 email, Bow Ho3 email, Thorsten Wohland1,4* email and Jeak Ling Ding1,5* email

Singapore-MIT Alliance, 117576, Singapore

Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, 117597, Singapore

Department of Chemistry, National University of Singapore, 117543, Singapore

Department of Biological Sciences, National University of Singapore, 117543, Singapore

author email corresponding author email* Contributed equally

BMC Biology 2009, 7:22doi:10.1186/1741-7007-7-22

Published: 11 May 2009

Additional files

Additional file 1:

Biochemical testing of S1 and the control peptide negS1. (A) Fluorescence emission spectra of negS1 in buffer (dotted line) or in POPS (dash-dot line). For comparison S1 in buffer (solid line) and in POPS is shown (dashed line) (B) Recombinant Factor C activation assay using negS1 (open triangle) and S1 (solid circle). The activation of Factor C without lipopolysaccharide binding peptide is displayed as a solid square. The samples contained 125 nM of the peptides or no peptide. (C) Fluorescence spectroscopy of Qdot655 labeled Escherichia coli. After subtraction of the E. coli auto-fluorescence the biotin-Qdot showed a signal close to zero (dotted line). In contrast, there was a clear fluorescence peak for S1-Qdot labeled cells (solid line), negS1-Qdot show only minor fluorescence (dashed line). Settings: Excitation 488 (15 nm), Emission 600–750 (15 nm).

Format: EPS Size: 1.2MB Download file

Additional file 2:

Table S1. Quantification of S1-nanoparticles counted on 20 Escherichia coli cells (total particle count 254) in transmission electron microscopy micrographs.

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