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CSE 599 Lecture 4: DNA computing
Cells process and store information
DNA forms an instruction manual
for the chemical processes in a cell
DNA stores hereditary information
passed from parents to offspring
Information is encoded digitally as
nucleotide sequences in the DNA
Thanks to Chris Diorio and Doug Zonker
for some of the slides
Deoxyribonucleic acid (DNA) (a) inside,
and (b) outside, the cell nucleus
Used figures from “Understanding DNA”
by Calladine and Drew
R. Rao, Week 4: DNA computing
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Digital Representation
Rather than thinking “biology” or “molecule,” think in terms
of digital information storage using the alphabet A, T, G, and C
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Biomolecular computing: Basic Idea
A DNA strand encodes a quaternary (2-bits/base) string
Can use molecular techniques to manipulate strings
Synthesize, cut, splice, copy, replicate and read DNA molecules
Separate and classify strings according to their size or content
These processes are slow but massively parallel
DNA for general-purpose digital computation
Encode: Map problem onto DNA strands
Exhaustive Search:
Generate all possible solutions by subjecting strands
simultaneously to biochemical reactions
Use molecular techniques to eliminate invalid solutions
The result: Turing Universal DNA computing
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DNA primer...
DNA provides cells with long-term information storage
Resides within cell nucleus
Provides templates for protein manufacture
mRNA is a temporary copy created from DNA
Migrates out of nucleus into cytoplasm
Ribosomes read mRNA to create proteins
Assisted by tRNA
Proteins perform cell functions
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Components of DNA/RNA
nitrogenous bases
purines
pyrimidines
thymine in DNA
uracil in RNA
pentose sugar
2-deoxyribose in DNA
ribose in RNA
phosphate group
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Nucleotides
base + sugar = nucleoside
nucleoside + phosphate = nucleotide
bases are linked into a chain by
alternating sugars and phosphates
direction is significant
read from 5’ end to 3’ end
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DNA base pairing (Watson-Crick
Complementarity)
Antiparallel strands form
hydrogen bonds between bases
Pairing of bases
cytosine guanine (C-G)
thymine adenine (T-A)
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DNA double helix
Cells are filled with water
Sugar–phosphate group is hydrophilic
Bases are hydrophobic
DNA double-strand twists to shield bases from water
10 – 12 bp/turn
Forms a helix
Human DNA strands can be 3cm long
but only 20Å in diameter
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DNA replication
“…it has not escaped our notice that the
specific pairing we have postulated
immediately suggests a possible copying
mechanism for the genetic material.”
- Watson & Crick
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mRNA production from DNA
Producing mRNA
1. Unwind section of DNA
2. Catalyze mRNA using RNA
polymerase
Base pairing
40 bases/sec at 37° C
3. DNA reforms into double helix
4. mRNA leaves nucleus
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Amino acids and Proteins
20 amino acids. Each is a carbon atom with:
Amino (NH2) and carboxyl (COOH) groups
A H+ atom (except proline) & something else
Protein: A chain of amino acids
Order of amino acids is primary structure
Backbone folding gives secondary structure
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mRNA allows protein synthesis
Base triplets (codons) code for
amino acids
Ribosomes serve as decoding
machines
tRNA is the adapter molecule
One end of tRNA carries an
amino acid
Other end carries an anticodon
that matches codon on mRNA
strand
When a ribosome finds a tRNA
with a matching anticodon,
amino acid is broken off and
attached to polypeptide chain
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The genetic code
Triplets code for amino
acids
AUG signals start of
translation
UAA, UAG, UGA signal
end of translation
Redundancy: Many triplets
may code for 1 amino acid
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A List of Molecular Techniques and Tools
Separating and fusing DNA strands: Denaturation (melting)
and Hybridization (also called annealing or renaturation)
Amplifying DNA: PCR (polymerase chain reaction)
Shortening and Cutting DNA (based on exonucleases and
endonucleases)
Determining the length of DNA (gel electrophoresis)
Reading the contents of DNA (DNA sequencing)
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Denaturation and Hybridization
Double helix can be denatured
by heating (85-95 degrees C)
Denaturing is reversible by
cooling (renaturing)
Called hybridization when DNA
is from different sources (e.g.
DNA and RNA)
The ability of two nucleic acid
preparations to hybridize is a
precise test for Watson-Crick
complementarity of their base
sequences
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DNA melting from heating
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PCR amplifies DNA
PCR: Polymerase chain reaction
Polymerase: Enzyme that adds
nucleotides to an existing DNA
strand in the 5’-3’ direction
Amplifies short segments of DNA
Doubling in ~5 minutes
Segment must be bracketed by
known primer sequences
~20 bases
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Enzymes that shorten or cut DNA
Exonucleases shorten DNA
Remove nucleotides one at a
time from the ends of DNA
molecules. E.g. ExonucleaseIII
removes nucleotides from the
two 3’ ends
Endonucleases cut DNA
E.g. Restriction enzymes such as
EcoRI recognize a short
sequence of DNA and cut the
molecule at that site
Recognition site typically 4-6
bases (e.g. GAATTC)
Sticky ends – overhanging ends
of DNA available for bonding
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Gel electrophoresis determines length
DNA molecules are negatively
charged
Place DNA on gel in electric field
DNA molecules drift through gel
toward positive electrode
Small molecules move faster
through gel than large ones
Deactivate field when first
molecules reach positive electrode
Determine lengths by comparing
distance of a sample with distance
traveled by control fragments with
known lengths
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Sequencing DNA
Break DNA at some instance of
known site
E.g. break DNA strands at G
Determine length of broken strands
Do this also for A, T, and C.
Electrophorese the results on one gel
Read out sequence from right to left
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DNA computing
Field started by Leonard M. Adleman (USC)
Used DNA strands and molecular techniques to solve a simple
Hamiltonian path problem:
Find a path that visits all vertices once and only once
Nov. '94 issue of Science magazine
Molecular Computations of Solutions to Combinatorial Problems
Laboratory experiment
Constructed DNA molecules representing the possible solutions
to a 7-city travelling salesperson problem
Details: see copy of paper that was handed out in class
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The computational premise
Construct a DNA molecule for each potential solution
Generate candidate solutions in parallel
Use molecular operations to eliminate invalid solutions
Five basic operations
Extract: Separates 1 DNA tube into:
One tube with all molecules containing a particular substring
Another with the remaining molecules
Merge: Mixes two tubes
Detect: Checks if there are any DNA strands in a tube
Copy: Amplifies the strands in a tube
Append: Attaches a string to the end of every molecule in a tube
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Adleman’s DNA-based encoding of graphs
Input graph:
Encoding:
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Basic Steps in Adleman’s Algorithm
Input: A directed graph G with n vertices, a start vertex vin and
a stop vertex vout
Step 1: Generate paths in G randomly in large quantities
Step 2: Reject all paths that do not begin with vin and end in
vout
Step 3: Reject all paths that do not involve exactly n vertices
Step 4: For each vertex v, reject all paths that do not involve v
Output: “Yes” if any path remains, “No” otherwise
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Adleman’s experiment
Took 7 days to solve 7-city problem, mainly due to
laboratory-related set-up time; Robotic manipulators could
speed things up
All steps are amenable to molecular implementation
Related Problems:
SAT: Solution proposed by Lipton
Created a directed graph whose paths correspond to all possible
Boolean assignments of variables
Search paths for a satisfiable assignment according to the
structure of input formula
Cracking the DES (data encryption standard)
Search for correct 56-bit key given (plaintext, cryptotext) pairs
Not done yet: at 1 operation/hour, requires 9 months
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Reasons to be optimistic...
DNA computing is orders of magnitude more energy and
density efficient than digital computers
Employs massive parallelism
Field is only 7 years old, so many untried paths
Example: Use the structure of DNA and proteins to compute?
Living cells hold many secrets
Copy their information-processing approaches
Possibly use living cells in computing systems
DNA can form self-assembling structures
Analogous to cellular automata
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Reasons to be pessimistic...
Generate-and-test approach requires one strand of DNA for
each candidate solution
270 DNA strands of length 1000 is 8 kilograms
DNA processing is slow and error prone
1 hour per reaction
Approximate matches and mutations may give incorrect results
Need to learn to build reliable computers from noisy components
No communication between strands
No easy way to determine if a tube contains two identical strands
No killer app has been identified yet
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Homework Assignment (due in two weeks)
Solve the SUBSET SUM problem using DNA computing
SUBSET SUM: Given a set of N positive integers S0, S1, …
, SN and a positive integer T (the "target"), is there some
subset of these integers Si (with possible repetitions) that
sums exactly to T?
Examples:
Input: S = { 2, 4, 6, 8, 10 }, T = 12; Answer: Yes
Input: S = { 2, 4, 6, 8, 10 }, T = 13; Answer: No
Input: S = { 1, 5, 4, 2, 7, 2, 12, 19, 17}, T = 42; Answer: Yes
(T = 1 + 5 + 5 + 2 + 12 + 17 or 1 + 1 + … + 1)
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Homework Assignment (cont.)
Three parts:
Encode a given problem instance using DNA strands
List the steps that will allow you to extract an answer
Implement your idea using the Strand software package for high
level simulation of DNA computing
Strand C++ Class Library:
Simulates the creation of DNA strands
Basic representation: short strand of DNA = an “Element”
Does not use individual bases or base sequences
High level simulation of typical operations performed in DNA
computing: melt, anneal, cut, detect, extract, remove, pour, append,
read, and length.
Documentation: http://www.lut.fi/~kyrki/dna/doku.html
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Next Week: Fundamentals of Neurobiology
No homework due next week.
Read the on-line articles for additional information on DNA
computing
Download and test the simulator using sample programs for
the Hamiltonian path and SAT problems
Contact TA or instructor if you have any questions or
problems regarding the DNA computing assignment
Have a great weekend!
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