Lecture 1 biochips
Transcript of Lecture 1 biochips
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Introduction to BioMEMS & BionanotechnologyLecture 1
R. BashirR. BashirLaboratory of Integrated Biomedical Micro/Nanotechnology and
Applications (LIBNA), Discovery ParkSchool of Electrical and Computer Engineering,
Weldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana
http://engineering.purdue.edu/LIBNA
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Key Topics
• Biochips/Biosensors and Device Fabrication• Cells, DNA, Proteins• Micro-fluidics• Biochip Sensors & Detection Methods • Micro-arrays• Lab-on-a-chip Devices
DNABacteria Proteins MoleculesVirusesCells
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Definitions
• BioMEMS are biomedical or biological applications of MEMS (micro electro mechanical systems)
• BioNanotechnology is biological applications of nanotechnology (science and technology of miniaturization at scales of <100nm)
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Apply micro/nano-technology to develop novel devices and systems that have a biomedical impact or are bio-inspired
BioMEMS and Bionanotechnology
Novel Solutions for Frontiers in Medicine and Biology
Novel Solutions for Frontiers in Materials
and InformationProcessing
Biology & Biomedicine
Micro/Nanotechnology and Systems
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Fea
ture
Siz
e
10nm
100nm
1µm
10µm
1nm
0.1nm
100µm
On Size and Scale !
Plant and Animal Cells
Most Bacteria
Min Feature of MOS-T (in 2004)
Virus
ProteinsOne Helical Turn of DNA
Gate Insulator for 100nm MOS-T
Atoms
Top-down
Bottoms-Up
MEMS
Nan
osc
ale
fun
ctio
nal
elem
ents
Mic
roE
lect
ron
ics
& M
EM
S
Integrated BioChips
(Macro, Micro, Nano)
Micro-fluidicsMolecularDevices
&Memory
Molecule-SpecificSensors
MEMS/NEMS
2-D CMOS platform
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More Definitions
• Biosensors are ‘analytical devices that combine a biologically sensitive element with a physical or chemical transducer to selectively and quantitatively detect the presence of specific compounds in a given external environment’ [Vo-Dinh and Cullum, 2000].
• Biochips can be defined as ‘microelectronic-inspireddevices that are used for delivery, processing, analysis, or detection of biological molecules and species’ [Bashir, 2004]. These devices are used to detect cells, microorganisms, viruses, proteins, DNA and related nucleic acids, and small molecules of biochemical importance and interest.
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Overview of Biosensor System
Sample Processing/Separation
Detection/ID
Data Analysis/Results• Water
• Food• Air• Body
Fluids
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Introduction
W.J. Chang, D. Akin, M. Sedlek, M. Ladisch, R. Bashir, Biomedical Microdevices, vol. 5, no. 4, pp.
281-290, 2003.
Key Attributes of Biochips1. Small length scale2. Small thermal mass3. Laminar flow, Re < 14. High surface-to-volume ratio
Whitesides Harvard University
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Reasons for Miniaturization
• In general, the use of micro and nano-scale detection technologies is justified by, – (i) reducing the sensor element to the scale of the
target species and hence providing a higher sensitivity à single entity/molecule
– (ii) reduced reagent volumes and associated costs,– (iii) reduced time to result due to small volumes
resulting in higher effective concentrations, – (iv) amenability of portability and miniaturization of the
entire system– (v) point-of-care diagnostic,– (vi) Multi-agent detection capability– (vii) Potential for use in vitro as well as in vivo
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• Applicationso Medicineo Pharmaceuticalso Food Safetyo Homeland Security, etc.
• Integrated, Sensitive, Rapid, Cost x Performance
• Commercialized; Nanogen, Affymetrix, Caliper, Others….
Biochips for Detection
DNABacteria Proteins MoleculesVirusesCells
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Novel Tools for NanoBiology
stimulus
Real-timebio-chemical
communication
Electrical
cellReal-timebio-chemical
communication
Electricalor Optical
Signals
cell
Controlled Microenvironment in a Biochip
Transcription factors:Proteins that control the transcription of specific genes
DNA
mRNA
Proteins
Transcription
Translation
Cell
• Analysis of single cells and the study of their function in real time. • Increase understanding of signaling pathways inside the cell. • Basic cell functions such as differentiation, reproduction,
apoptosis, etc. and their implications on various disease states. • Focus of the post-genomic era and systems biology
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BioChip/BioMEMS Materials
• Silicon and microelectronic materials• Glass, Quartz• Polymers
– Poly (dimethylsiloxane) (PDMS)– Poly (methyl methacrylate) (PMMA)– Teflon, etc.
• Biological Entities– Cells, Proteins, DNA– Frontier of BioMEMS !
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Introduction to Device Fabrication• MEMS/NEMS Silicon Fabrication
– Formation of structures that could be used to form sensors and actuators.
– Processing of electrical or non-electrical signals. – Conventional and new semiconductor processing technology modules
are used. – Etching, Deposition, Photolithography, Oxidation, Epitaxy, etc.– Deep RIE, Thick Plating, etc
• Bulk and Surface Micromachining
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From Dec 1996, Electron IC Design
Bulk Micromachined Accelerometer from Silicon Microstructures. Inc.
Probes for AFM
DMD Chip from Texas Instruments
MEMS Examples
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Single Chip Accelerometer
(Analog Devices)
Chip
Sensor
Deployment of air-bag
MEMS Examples
SiMembrane
Etch Cavity
Draper Labs, National Semiconductor, 1998
Au back-plate
Single Chip Microphone
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Silicon BioMEMS Examples
Kumetrix Purdue Silicon BioChip IBM Zurich Research
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BioMEMS/Biochip Fabrication
• In addition to Silicon….• Biocompatibility, ideal for biomedical
devices• Transparent within the visible
spectrum• Rapid fabrication• Photo-definable• Chemically modifiable• Possible choices
– PDMS - polydimethylsiloxane, – Hydrogels – PMAA, – Teflon– SU-8, etc.
Lab on Chip (Caliper)
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Alternative Fabrication Methods
• Soft Lithography– Replication and molding– Micro-contact printing– Micro-molding in capillaries– Micro-transfer molding– Solvent assisted micro-molding– Dip Pen Lithography
• Compression Molding– Hot Embossing– Injection Molding
• Inkjet Printing
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Replication and Molding
• Master mold made from silicon, glass, metal, SU-8
• Surface treatment of master• Pour PDMS (mix, oligomer,
and CL agent)• Cure (~60C, 1 hr)• Peel off PDMS structure• Mold can be used again• Y. Gia, and G. M. Whitesides,
Annu. Rev. Mater. Sci. 1998, 28, 153-84
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µ-Contact Printing
• Ink the PDMS structure with molecules (alkylthiols, proteins, DNA, etc.)
• Transfer the layer through physical contact (optimize time)
• Inking is performed via covalent binding on substrate
• Can be performed on flat surface or curved surface
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PDMS/Glass (Silicon) Hybrid Biochip
Silanized silicon mold
PDMS 1st layer(a)
PDMS 2nd layer(c)
Teflon tubing(b)
Horizontal channel(d)
Opening sealed with PDMS
(e)Vertical channels
(f)(f)
(g)
Bonding on top of silicon chip
Connection of tubingsfor the flow of liquid
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OutputTube
Input Reservoir
in 3rd Layer of PDMS
1st Layerof PDMS
2nd Layerof PDMS
Silicon
Oxide
Metal
Bonding with PDMS
Input Reservoir
in 3rd Layer of PDMS
1st Layerof PDMS
2nd Layerof PDMS
ChipUnderneath
Silicon Base, 3 PDMS layers, Top I/O port
Glass Base, 3 PDMS layers, Top I/O port, Valves
Air channels
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Dip Pen Lithography
• AFM Tip used to ‘write’molecules
• Being commercialized by Nanoink, Inc.
• SAMs, DNA, Proteins, etc.• Serial (need array of cantilevers
for parallel writing)• Continuous source of
molecules – microfluidics !
Lee, K.B.; Park, S.J.; Mirkin , C.A. ; Smith, J.C.; Mrksich, M.Protein nanoarrays generated by dip-pen nanolithography Science 2002 , 295, 1702-1705.
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Compression Molding
Hot Embossing Precision Injection Molding
Polymer (thermoplastic material)
MoldHeat
Pressure
Substrate
Features down to 0.1um deep and 0.6um wide (for
CD-R)
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Nano-Imprint Lithography
• Nano-scale extension of hot embossing
• Need a nano-scale master mold• Added to ITRS Roadmap
Steve Chou, Princeton U.
Imprint mold with 10nm
diameter pillars
10nm diametermetal dots
10nm diameter holes imprinted in
PMMA
Substrate
Substrate
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Key Topics
• Biochips/Biosensors and Device Fabrication• Cells, DNA, Proteins• Micro-fluidics• Biochip Sensors & Detection Methods • Micro-arrays• Lab-on-a-chip Devices
DNABacteria Proteins MoleculesVirusesCells
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Cells – Brief Overview• Genetic information is
contained in chromatin (a diffused mass which distinguishes to a chromosome when cell is ready to divide)
• Humans have 46 chromosomes in each cell (except in reproductive cells)
• Chromosomes are long, uninterrupted, packed, super-coiled linear polymer strands of DNA (deoxyribonucleic acid) - 6 cm long when extended
• In humans, each chromosome is 50-400 x 106 units long
From: Biology, 4th Edition by Campbell
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Transcription factors:Proteins that control the transcription of specific genes
DNA
mRNA
Proteins
Transcription
Translation
Cell
Cells – Brief OverviewSurface Proteins
(could be specific to cells)
YY
http://gslc.genetics.utah.edu/units/basics/transcribe/
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DNA to Proteins• Transcription
– double stranded DNA is converted to a single stranded mRNA
– RNA polymerase synthesizes the mRNA
• Translation– Ribosomes ‘translate’ the
sequence of bases in the mRNA to proteins.
– These proteins than perform various functions inside and outside the cell
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Dec
reas
ing
com
plex
ity
Chromosomes à DNA
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Structure of DNA
• DNA is composed of;– a phosphate back-bone
where each phosphate radical has a negative charge
– a Deoxyribose (D in DNA) sugar
– 4 types of bases or nucleotides. These are adenine (A), thymine (T), cytosine (C), Guanine (G)
• A binds to T and G binds to C -complementary base pairs
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Pur
ines
(A, G
)2
ring
s
Pyr
imid
ines
(T, C
)1
rin
g
Structure of DNA
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DNA Hybridization
• When DNA is heated to a temperature (~>90°C) or exposed to pH > ~12, the complementary strands dissociates - DNA denaturation
• Process is reversible (exposure to a melting temperature Tm > 65°C) and 2 complementary ssDNA will hybridize to each other and join to form dsDNA
• Hybridization can happen between any two complementary single stranded molecules (DNA/DNA, DNA/RNA, RNA/RNA)
• Can provide a very sensitive means to detect specific nucleotidesequences
• Factors affecting hybridizaton : temperature, Salt and buffer concentration, G & C content - Tm can be calculated
• Rate of hybridization is proportional to concentration of target and probe and limited by the lower concentration material
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DNA Hybridization
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GC
CT A
GG
AA
AC
AC
C
CG T
T
G
G
CT A
TG
TA
AC
AG
C
C
GT
T
Reduced Stringency
Hybridization
Stringent Hybridization
Stringency
DNA Hybridization
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PCR - Polymerase Chain Reaction
• Technique to amplify (make multiple copies) of known DNA molecules - invented in 1985
• Use enzyme called DNA polymerase and primers (short ssDNA strands)
• Billions of copies can be made within hours in laboratory
• Very useful in research, diagnosis, forensics, etc where large samples are required from very small concentrations.
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PCR SequenceTe
mpe
ratu
re
Time
• Primers are short strands of nucleotides which are complementary to specific regions of the target DNA to the amplified -hence the ‘end’ sequence of short regions of the target DNA to be copied is needed • DNA Polymerase is an enzyme which takes nucleotides from the ambient solution and starts to construct the complementary sequence• An adequate supply of nucleotides are needed (dNTPs -deoxyribonucleose triphosphates -dATP, dCTP, dGTP, dTTP)
90C
55C
70C
RT
1. Denature
2. Anneal
3. Extend 90C
55C
70C
1. Denature
2. Anneal
3. Extend
15-30sec
15-30sec
30-60sec
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C R H
NH2
COOH
CR1 H
NH2
Peptide Bond
CR2 H
COOH
Peptide Bond
C R3 H
Peptide Bond
CR4 H
http://www.umass.edu/microbio/rasmol/rotating.htmhttp://www.umass.edu/microbio/chime/antibody/
Protein Structure