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Since the dawn of time, man has tried to record important events and techniques for
everyday life. At first, it was sufficient to paint on the family cave wall, how one hunted.
Then came the people who invented spoken languages and the need arose to record what
one was saying without hearing it firsthand. Therefore, year’s later; more early scholars
invented writing to convey what was being said. Pictures gave way to letters which
represented spoken sounds. Eventually clay tablets gave way to parchment, which gave
way to paper. Paper was, and still is, the main way people convey information. However,
in the mid twentieth century computers began to come into general use.
Evolution of Storage Media:
Computers have gone through their own evolution in storage media. In 1956, researchers
at IBM developed the first disk storage system. This was called RAMAC (Random
Access Method of Accounting and Control)
Since the days of punch cards, computer manufacturers have strived to squeeze more data
into smaller spaces. That mission has produced both competing and complementary data
storage technology including electronic circuits, magnetic media like hard disks and tape,
and optical media such as compact disks.
Today, companies constantly push the limits of these technologies to improve their speed,
reliability, and throughput -- all while reducing cost. Standard compact disks are also
gaining a reputation as an incredibly cheap way of delivering data to desktops. They are
the cheapest distribution medium around when purchased in large quantities (Rs. 18/- per
700 MB disk).
Holostore Technology:
This figure is still very impressive compared to today's magnetic storage densities, which
are around 100 Kb per square centimeter (not including the derive mechanism).
Molecular Memory:
The demands made upon computers and computing devices are increasing each year.
Processor speeds are increasing at an extremely fast clip. However, the RAM used in
most computers is the same type of memory used several years ago.
Currently, RAM is available in modules called SIMMs or DIMMS. These modules can be
bought in various capacities from a few 100KB to about 128 MB. These modules are
generally 7.5ns. Whereas a 5cu.cm block of bacteriorhodopsin studded polymer could
theoretically store 512GB of information. When this comparison is made, the advantage
becomes quite clear. Also, these bacteriorhodopsin modules could also theoretically run
1000 times faster.
Researchers are looking at protein-based memory to compete with the speed of electronic
memory, the reliability of magnetic hard disks and the capacities of optical/magnetic
storage. There have been many methods and proteins researched for use in computer
applications in recent years. The most promising approach is of 3D Optical RAM storage
using the light sensitive protein bacteriorhodopsin.
Early research in the field of protein-based memories yielded some serious problems with
using proteins for practical computer applications. Among the most serious of the
problems was the instability and unreliable nature of proteins, which are subject to
thermal and photochemical degradation, making room-temperature or higher-temperature
use impossible. Scientists stumbled upon bacteriorhodopsin, a light-harvesting protein
that has following properties which make it a prime candidate for computer applications.
A cyclicity (the number of times it can be photo-chemically cycled) which exceeds 106, a
value considerably higher than most synthetic photo chromic materials
High quantum yields (efficient use of light) which permits the use of low light levels for
switching/activating
Ability to form thin films or oriented polymer cubes containing bacteriorhodopsin with
excellent optical properties
The initial resting state for bacteriorhodopsin is called bR. When bR is exposed to
green light, in the range of approximately 550nm, it shifts to the K state. This K state is
an unstable state. So the bacteria cannot remain in this state for long thus, K relaxes
forming M. This M state is similar to K and is unstable. So it again relaxes forming the O
state. This state is quite stable.
If the O state is not exposed to a red light source, it will eventually relax back to
the bR state. However, if it is exposed, it will then undergo a reaction a called ‘a
branching reaction’. The O state will shift to the P state and then to the Q state – a form
that remains stable almost indefinitely for years. Blue light will, however, convert Q back
to bR. Of the six states – bR, K, M, O, P and Q – only the most stable ones are
particularly useful.
GREEN
LIGHT
SOURCE
b BLUE
LIGHT
R
CONVERTS CONVERTS SOURCE
K Q
RELAXES RELAXES
M P
RELAXES CONVERTS
RED LIGHT
SOURCE
The two – photon method is superior to a single photon method when using three –
dimensional memory. This is because a single photon would excite all of the molecules
that it came into contact with, where a two – photon method would only excite the
molecules at the location where they intersect.
A two photon mechanism is able to excite molecules inside the volume of memory,
without exciting the surface molecules. Each photon itself does not have enough energy
to excite the molecules to the next higher energy state. Also no real state exists at the
energy of either photon alone. Absorption will occur if the sum of the energies of each
photon is equal to or greater than the energy gap of the transition, and only in the volume
where the two photons overlap.
This process would allow reading and writing anywhere in the volume of the RAM where
the sequential method must start at the surface of the RAM. At the point of absorption
where the two photons intersect, a molecular change will occur in that micro volume.
This will distinguish it from the rest of the unexcited molecules. The two molecular
structures provide for a read and write state, or 0 and 1 state in the RAM.
Basically, the unit is a thin wafer of protein, sandwiched between glasses and sealed off
with two Teflon gaskets and black anodized aluminum. The protein wafer is formed by
creating a matrix of bacteriorhodopsin strands within a polymer gel. The ribbon-like
nature of the protein naturally lends itself to the formation of this matrix. It also makes it
easier for the device to read the data.
Furthermore, at the base of the cuvette is a temperature base plate capable of heating or
cooling the bacteriorhodopsin. This alters the physical properties of the bR when needed
and cools the matrix when the cuvette becomes hot.
Sandwich
A single matrix element of the opticom memory is supposed to have a dimension of less
than 100nm. The entire layer is 350nm thick. This is 10 to 100 times smaller than the
common size of microchips. Thus the usual lithographic procedures could not be sued in
the production process. Dimensions that small could actually be achieved if the matrix’s
strip conductors are made of (conductive) polymers. The polymer chains, which are only
a few nm thick, but quite long, line themselves up under certain conditions, thus serving
as one of the matrix lines. The second polymer layer could also possibly be structured by
exposure to UV light.
The catch with organic memory is the connections of this matrix. Every single strip
conductor of the matrix must be connected to and powered by a transistor. The
dimensions of modern transistors in 0.25 aem technology pose an obstacle of a few
micrometers to the measurements of opticom’s dream memory with 100nm line intervals.
In addition, the mini strip conductors have to contact the giant transistor connectors in a
confined area.
Opticom polymer memory: a matrix addresses the light emitting polymers. The light
“writes” on the proteins in the middle of the sandwich at a cross point. The lower
polymer layer absorbs light thus reading the memory content
Laser Array 1
bR
MEMORY CUBE
Bacteriorhodopsin, after being initially exposed to light (in our case a laser beam) will
change to between photo-isomers during the main photochemical event when it absorbs
energy from a second laser beam. This process is known as sequential one-photon
architecture, or two-photon absorption. While early efforts to make use of this property
were carried out at cryogenic temperatures (liquid nitrogen temperatures), modern
research has made use of the different states of bacteriorhodopsin to carry out these
operations at room-temperature. The process breaks down like this:
Upon initially being struck with light (a laser beam), the bacteriorhodopsin alters its
structure from the bR native state to the O state. After a second pulse of light, the O state
then changes to the P form, which quickly reverts to a very stable Q state, which is stable
for long periods of time (even up to several years).
The data writing technique proposed by Dr. Berge involves the use of a three-dimensional
data storage system. In this case, a cube of bacteriorhodopsin in a polymer gel is
surrounded by two arrays of laser beams placed at 90 degree angles from each other. One
array of lasers, all set to green (called "paging" beams), activates the photo cycle of the
protein in any selected square plane, or page, within the cube. After a few milliseconds,
the number of intermediate O stages of bacteriorhodopsin reaches near maximum. Now
the other set, or array, of lasers - this time of red beams - is fired.
The second array is programmed to strike only the region of the activated square where
the data bits are to be written, switching molecules there to the P structure. The P
intermediate then quickly relaxes to the highly stable Q state. We then assign the initially-
excited state, the O state, to a binary value of 0, and the P and Q states are assigned a
binary value of 1. This process is now analogous to the binary switching system which is
used in existing semiconductor and magnetic memories. However, because the laser array
can activate molecules in various places throughout the selected page or plane, multiple
data locations (known as "addresses") can be written simultaneously - or in other words,
in parallel.
The system for reading stored memory, either during processing or extraction of a result
relies on the selective absorption of red light by the O intermediate state of
bacteriorhodopsin. To read multiple bits of data in parallel, we start just as we do in the
writing process. First, the green paging beam is fired at the square of protein to be read.
After two milliseconds (enough time for the maximum amount of O intermediates to
appear), the entire red laser array is turned on at a very low intensity of red light. The
molecules that are in the binary state 1 (P or Q intermediate states) do not absorb the red
light, or change their states, as they have already been excited by the intense red light
during the data writing stage.
Laser Array 1
RED
LASER
bR CUBE
However, the molecules which started out in the binary state 0 (the O intermediate state),
do absorb the low-intensity red beams. A detector then images (reads) the light passing
through the cube of memory and records the location of the O and P or Q structures; or in
terms of binary code, the detector reads 0's and 1's. The process is complete in
approximately 10 ms, a rate of 10MB per second for each page of memory.
Erasing the data is even simpler. One method would be to simply fire a deep blue paging
beam through the cube. This would erase an entire page of data in one shot.
If data in one row or one location is to be erased, simply fire two low – intensity
orthogonal laser beams in the cubic matrix. Where they meet, the intensity of the beam
will be doubled. Thus, it would provide the necessary intensity to change the state of the
molecule back to bR. The other locations hit by the low intensity beams would begin to
absorb the light. But, the intensity would not be enough to cause a state shift.
Latest Developments
Small enough to be incorporated onto standard computer boards, these optical computer
memory systems will be interfaced to advanced computer architectures for high-speed
processing. Indeed, we are on the threshold of a new exciting era in the wonderful world
of computing. And every possibility is there, that in the near future we will be able to
carry a small encyclopedic cube containing all the information we need and retrievable at
the speed of light!!!
References
www.cem.msu.edu
www.ieee.org
www.sciamarchive.com
Protein-Based Optical Computing and Memories, Berge, Robert R., scientific American
magazine – March 1995.
Steve Redfield and Jerry Willenbring "Holostore technology for higher levels of memory
hierarchy," IEEE potentials, 1991, PP. 155-159
Najeeb Imran, "Optical computing," IEEE potentials, Dec 1992, PP. 33-36 Tom
Thomson, "What's Next, "Byte, April 1996, PP. 45-51
CONTENTS
1. INTRODUCTION
3. HOLOSTORE TECHNOLOGY
4. MOLECULAR MEMORY
5. PROTEIN-BASED MEMORY
6. PHOTO CYCLE
9. SANDWICH
10. DATA
Fig: Arrangement for data storage into bRWRITING
cube TECHNIQUE
15. CONCLUSION
16. REFERENCES