Supporting Information

Similar documents
Supporting Information. Time-Resolved Botulinum Neurotoxin A Activity Monitored using. Peptide-Functionalized Au Nanoparticle Energy Transfer Sensors

Detection of Mercury(II) and Lead(II) with Graphene Oxide- Based Biosensors

Supporting Information

Triangulating Nucleic Acid Conformations Using Multicolor Surface Energy Transfer

single-molecule fluorescence resonance energy transfer

Protein-based Sensitive, Selective and Rapid Fluorescence Detection of Picric Acid in Aqueous Media

Energy transfer and optical gain studies of FDS: Rh B dye mixture investigated under CW laser excitation

Electronic Supporting Information Measuring Viscosity inside Mesoporous Silica Using Protein-Bound Molecular Rotor Probe

Mercury(II) detection by SERS based on a single gold microshell

Fluorescence (Notes 16)

[Supporting Information]

Fluorescence Spectroscopy

Fluorescence resonance energy transfer from a β-carboline analogue to a cationic photosensitizer in aqueous solution

Supporting Information

The peptides were synthesized manually using in situ neutralization cycles for Boc-solid

Single-Molecule Methods I - in vitro

FROM LOCALIZATION TO INTERACTION

Protein quantification and detection methods

Electrical control of near-field energy transfer between. quantum dots and 2D semiconductors

Supporting Information

4 Single molecule FRET

Co-localization, FRET

1. Transition dipole moment

arxiv: v1 [physics.optics] 8 Jan 2015

Fluorescence 2009 update

Multi-color broadband visible light source via GaN hexagonal. annular structure

Förster Energy Transfer - AKA - Fluorescence Resonance Energy Transfer

Degree of labeling (DOL)

The photoluminescent graphene oxide serves as an acceptor rather. than a donor in the fluorescence resonance energy transfer pair of

Techniques in Molecular Genetics Spectroscopy and Enzyme Assays

Fluorescence Resonance Energy Transfer (FRET) Microscopy

Experiment 1 (Part A): Plotting the Absorption Spectrum of Iron (II) Complex with 1,10- Phenanthroline

Electronic Supplementary Information (ESI) for. biosensing platform through the coupling of nanometal surface

Supplemental Materials and Methods

λmax = k d Supplementary Figures

Figure S1. Experimental design for the GSH-coated AuNP studies.

Fluorescence Spectroscopy

1. Strahlungsgesetze, Ableitung der Planck-schen Strahlungsformel, Einstein-Koeffizienten, Extinktinskoeffizient, Oszillatorenstärke

Supplementary Material

1 Fluorescence Resonance Energy Transfer

6. A solution of red Kool-Aid transmits light at a wavelength range of nm.

Fluorescence Resonance Energy Transfer (FRET) in Polymer Films and Polymer Blends

Detection of toxic mercury ions using a ratiometric CdSe/ZnS nanocrystal sensor

Laser. emission W FL

Photoluminescence enhancement of carbon dots by gold. nanoparticles conjugated via PAMAM dendrimers

Facile bulk production of highly blue fluorescent

Supporting Information. Supramolecular Host-Guest Chemistry-based Folate/Riboflavin Functionalization and. Cancer Cell Labeling of Nanoparticle

Supplementary information for. Observation of photovoltaic action from photoacid-modified Nafion due to light-driven ion transport

Protocol for Coating QD-COOH on glass slides Chris Ochs 19/09/12 Modified by Kathy Lu 2/27/2013

Application Note: Ocean Optics in the Teaching and Research Laboratories Susquehanna University Department of Chemistry July 2014

Multiplexible Wash-Free Immunoassay Using. Colloidal Assemblies of Magnetic and. Photoluminescent Nanoparticles

Reconfigurable DNA Origami Nanocapsule for ph- Controlled Encapsulation and Display of Cargo

Plasmon-Enhanced Energy Transfer in Photosensitive Nanocrystal Device. Hilmi Volkan Demir 1,4 *

Influence of Plasmonic Array Geometry on Energy Transfer from a. Quantum Well to a Quantum Dot Layer

Novel Nanoparticles for Ultrasensitive Detection and Spectroscopy

Lambert s law. Beer s law. di x / I x = -kdx (-di x = k I x dx) = - a c dx. I/I 0 = e -kl T = A = - log (T) = - log (I/I 0 )

Modulating Enzymatic Activity in the Presence of Gold Nanoparticles

CHEM Outline (Part 15) - Luminescence 2013

IRDye 800CW Protein Labeling Kit Low MW

Quantification of ligand packing density on gold nanoparticles using ICP-OES

Supporting Information

X-ray induced singlet oxygen generation by. nanoparticle-photosensitizer conjugates for. photodynamic therapy: determination of singlet

Supplemental Information for

Lecture 5. Anisotropy decay/data analysis. Enrico Gratton

Digitized single scattering nanoparticles for probing molecular binding

Stable Encapsulation of Quantum Dot Barcodes with Silica Shells

Fundamentals of nanoscience

Functionalization of Cellulose Nanocrystals with PEG-Metal- Chelating Block Copolymers via Controlled Conjugation in Aqueous.

Supporting Information

Chapter 2 Energy Transfer Review

CD Basis Set of Spectra that is used is that derived from comparing the spectra of globular proteins whose secondary structures are known from X-ray

Instantaneous and Quantitative Functionalization of Gold Nanoparticles with Thiolated DNA Using a ph-assisted and Surfactant-Free Route

Supporting Information (SI) for

Quantification of NS1 dengue biomarker in serum via optomagnetic nanocluster detection

Lithography-Free Broadband Ultrathin Film. Photovoltaics

Supplementary figure 1 Application of tmfret in LeuT. (a) To assess the feasibility of using tmfret for distance-dependent measurements in LeuT, a

Ultrafast single photon emitting quantum photonic structures. based on a nano-obelisk

A very brief history of the study of light

Supplementary Materials: Size Control and Fluorescence Labeling of Polydopamine Melanin Mimetic Nanoparticles for Intracellular Imaging

Silicon Nanoparticles with Surface Nitrogen: 90% Quantum Yield with Narrow Luminescence Bandwidth and the Ligand Structure Based Energy Law

Supporting Information

Luminescent Probes and Photochromic Switches Based on Semiconductor Quantum Dots

Supporting information. One-step facile synthesis of novel β-amino alcohol functionalized

High photostability and enhanced fluorescence of gold nanoclusters by silver doping-supporting information

Fluorescence and Nuclear Magnetic Resonance (NMR) Spectroscopy

Aula 5 e 6 Transferência de Energia e Transferência de Elétron Caminhos de espécies fotoexcitadas

Supporting Information

Protein assay. Absorbance Fluorescence Emission Colorimetric detection BIO/MDT 325. Absorbance

Chiral Surface of Nanoparticles Determines the Orientation of Adsorbed Transferrin and its Interaction with Receptors

Luminescence. Photoluminescence (PL) is luminescence that results from optically exciting a sample.

Single Emitter Detection with Fluorescence and Extinction Spectroscopy

Surface Plasmon-Induced Hot Carrier Effect on Catalytic Activity of CO oxidation on Cu 2 O/Hexoctahedral Au Inverse Catalyst

Zinc-Phosphorus Complex Working as Atomic Valve for Colloidal Growth of Monodisperse Indium Phosphide Quantum Dots

Semiconductor quantum dots

The ROXI Colorimeter & Fluorimeter. Laboratory Application I. Colorimetric measurements via Beer s Law.

Quantum Dot-Peptide-Fullerene Bioconjugates for Visualization of In Vitro and In Vivo Cellular Membrane Potential

Supporting Information for. Coumarin-derived Cu 2+ Selective Fluorescence Sensor: Synthesis, Mechanisms, and Applications in living cells

Quantum Dots as Immunoassay Probes. Roger M. Leblanc

two slits and 5 slits

Interactions Between Localized Surface Plasmons and Molecular Resonances

Transcription:

Supporting Information Energy Transfer-Based Multiplexed Assay of Proteases by Using Gold Nanoparticle and Quantum Dot Conjugates on a Surface Young-Pil Kim, 1, Young-Hee Oh, 1, Eunkyu Oh, 1 Sungho Ko, 2 Min-Kyu Han, 1 and Hak- Sung Kim 1 1 Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 305-701, Republic of Korea. 2 Korea Food Research Institute (KFRI), Sungnam-Si, Gyeonggi-Do 463-746, Republic of Korea Calculation of Förster distance, separation distance, and quenching efficiency for QD-dye and QD-AuNP pairs. To compare the quenching ability of various energy acceptors against QD, AuNP and Cy5 were tested by employing QDs as donors. As described elsewhere, 1 the Förster distance (R 0 ) values of QD-AuNP and QD-cy5 were estimated by using the following formula: R 2 1/ 6 9000(ln10) κ Q D 3 0 J ( λ) = 9.79 10 5 4 D D ) NA128π n D 2 4 ( κ Q n J ( λ ) 1/ 6 = (Eq. 1) Where κ 2 is the relative orientation of the transition dipoles between the donor and acceptor, n D the refractive index of the medium, N A Avogadro number, Q D the quantum yield of the donor, J(λ) the overlap integral (cm 6 mole -1 ) of the donor emission and acceptor absorption spectra. The overlap integral is given by; 4 J ( λ) = PLD corr( λ) λ ε A( λ) dλ (Eq. 2) Where λ is wavelength, PL D-corr (λ) is normalized donor emission spectrum, and ε A (λ) is the acceptor absorption spectrum expressed as an extinction coefficient. 1

By using the above Förster formula (Eq. 1 and 2), the Förster radii of QD-AuNP and QD-Cy5 were calculated from the overlap integral (Figure S5) between the emission spectrum of the donor and the absorbance spectrum of the acceptor. We assumed that the quantum yield of SA-QD605 (Lot No. 47789A) was 0.55, and the refractive index of biomolecules was 1.4 in the aqueous solution. The orientation factor was assumed to be 2/3. The molar extinction coefficients of AuNP and Cy5 are 1.1 10 5 cm 1 M 1 at 420 nm and 2.5 10 5 cm 1 M 1 at 649 nm, respectively. Energy transfer between QDs and acceptors (AuNP or Cy5) can be determined based on the quenching efficiency (Q E ) of the experimentally obtained PL data. Considering multiple acceptors per quantum dot, the overall efficiency can be written as: Q 6 FDA nr0 E = 1 = (Eq. 3) 6 6 FD nr0 + r Where F D is the fluorescence intensity of the donor alone, F DA is the fluorescence intensity of the donor in the presence of the acceptor(s), r is a separation distance from the QD centre to the acceptors, and n is the number of surface-bound acceptors. From the experimentally determined quenching efficiency (Q E ), the above equation can be used to determine the D-A distance with calculated R 0 : 1/ 6 E ) n(1 Q r = R0 Q (Eq. 4) E A Stern-Volmer analysis for energy transfer. The Stern-Volmer relationship 2 between the quencher concentration and fluorescence intensity is; F0 = 1+ K D ( CQ ) (Eq. 5) F where F 0 and F are emission intensities in the absence and presence of quencher, respectively, 2

K D the Stern-Volmer quenching constant, and C Q the concentration of quencher. Quantification of protease activity. Surface-immobilized nanoprobes were reacted with varying concentrations of a protease at 37 C for 30 60 min. Protease activity were obtained by converting the recovered quenching efficiency to the concentration of cleaved peptides per min according to Eq. 6. Calibration curve for a protease was plotted as a function of protease concentration. Since the concentration of the nanoprobe was equivalent to respective protease reaction, different concentration ranges of protease were applied by taking into consideration the different specific activities (7500 Units per mg protein for MMP-7; 3280 Units per mg protein for caspase-3; 4000 Units per mg protein for thrombin). One Unit is defined as the amount of enzyme that cleaves 1 nmol of substrate per min. %Recovery = F F DA K '[ E] + E FDA M = (Eq. 6) F K + [ E] D+ E DA ' M Where F D+E is the PL intensity of the QD after enzyme reaction, F DA and F DA+E the PL intensities of the nanoprobes before and after enzyme reaction, respectively, K M the surface Michalelis-Menten constant, and [E] enzyme concentration. 3

4 3 F 0 / F 2 1 0 0 100 200 300 400 500 AuNP Conc. (nm) Figure S1. A Stern-Volmer analysis for energy transfer between QD and free AuNP. The inversed fluorescence intensities (F 0 /F, in Eq. 5) of donor QD was plotted as a function of free AuNP concentration (QD=10 nm). Each data point indicates the average of duplicate experiments, and the error bar represents the standard deviation. 4

120 QD only +Pep THR -AuNP 100 PL (%) 80 60 40 20 0 QD525 QD605 QD655 Figure S2. Changes in the PL intensities of QDs having different colors (SA-QD525, SA- QD605, and SA-QD655) in the presences of biotinylated Pep THR -AuNPs in solution. The molar ratios of Pep-AuNPs to respective QDs were equally maintained at 50. 5

80 Q E (%) 60 40 20 0 0 100 200 300 400 500 Pep-AuNP (nm) Figure S3. Standard curve for the Q E of SA-QD605 as a function of the concentration of Pep- AuNP (AuNP-CRPLALWRSK-biotin). The concentration of QD was 10 nm. Each data point indicates the average of quadruple experiments, and the error bar represents the standard deviation. 6

MMP-7 Donor signal (Exi 460/Emi 525) Acceptor signal (Exi 460/Emi 595) washing out (a) 0 ng/ml 1 Organic dye (TAMRA) QD (b) 10 ng/ml 1 Glass (c) 100 ng/ml 1 (d) 1 µg/ml 1 (e) 10 µg/ml 1 Intensity (I 525 /I 595 ) 2.0 1.5 1.0 0.5 0.0 (f) 100 µg/ml 1 10 0 10 1 10 2 10 3 10 4 10 5 10 6 MMP-7 Conc. (ng ml -1 ) (A) (B) (C) Figure S4. On-chip assay of protease activity based on the FRET between the donor SA- QD525 (green) and the acceptor TAMRA-labeled peptide (red). FRET intensity between the QD and TAMRA was plotted as a function of MMP-7 concentration, which ranged from 10 ng ml 1 to 100 µg ml 1. The error bar indicates the standard deviation in duplicate spots (I 525 : PL intensity of donor; I 595 : PL intensity of acceptor). 7

Normalized PL & ABS 1.2 1.0 0.8 0.6 0.4 0.2 (A) Normalized PL & ABS 1.2 1.0 0.8 0.6 0.4 0.2 (B) 0.0 450 500 550 600 650 700 Wavelength (nm) 0.0 450 500 550 600 650 700 Wavelength (nm) Figure S5. The overlap integral spectra between the emission of donor and the absorbance of acceptor. (A) Emission and absorbance spectra of QD605 (dotted line) and AuNPs (solid line), respectively. Fluorescence intensity of QD605 was normalized to the maximum extinction coefficient of AuNP (1.1 10 5 cm -1 M -1 at 420 nm. (B) Emission and absorbance spectra of QD605 (dotted line) and Cy5 (dashed line), respectively. Fluorescence intensities of QD605 were normalized to the maximum extinction coefficient of Cy5 (2.5 10 5 cm -1 M -1 at 649 nm). References (1) Förster, T. Ann. Phys. 1948, 2, 55-75. (2) (a) Lakowicz, J. R. Principles of Fluorescence Spectroscopy; Plenum Press: New York, 1983. (b) Keizer, J. J. Am. Chem. Soc. 1983, 105, 1494 1498. 8