A Study on DNA Memory Encoding Architecture

The amount of raw generated data is growing at an exponential rate due to the greatly increasing number of sensors in electronic systems. While the majority of this data is never used, it is often kept for cases such as failure analysis. As such, archival memory storage, where data can be stored at an extremely high density at the cost of read latency, is becoming more popular than ever for long term storage. In biological organisms, Deoxyribonucleic Acid (DNA) is used as a method of storing information in terms of simple building blocks, as to allow for larger and more complicated struc- tures in a density much higher than can currently be realized on modern memory devices. Given the ability for organisms to store this information in a set of four bases for an extremely long amounts of time with limited degradation, DNA presents itself as a possible way to store data in a manner similar to binary data. This work investigates the use of DNA strands as a storage regime, where system-level data is translated into an efficient encoding to minimize base pair errors both at a local level and at the chain level. An encoding method using a Bose-Chaudhuri-Hocquenghem (BCH) pre-coded Raptor scheme is implemented in conjunction with an 8 to 6 bi- nary to base translation, yielding an informational density of 1.18 bits/base pair. A Field-Programmable Gate Array (FPGA) is then used in conjunction with a soft-core processor to verify address and key translation abilities, providing strong support that a strand-pool DNA model is reasonable for archival storage

Skeletal Muscle Tissue Engineering System to Mimic In Vivo Development

Skeletal muscle atrophy can occur for a number of reasons including degenerative diseases and age-related sarcopenia. Current pre-clinical studies for regeneration therapies are solely reliant on animal models, which do not accurately mimic human tissue and chemistry. The purpose of developing this device was to provide a reproducible manner of creating an in vitro skeletal muscle model that will aid in preclinical therapy testing. The device was designed to maintain a sterile environment for tissue culture, which provides anchorage, periodic strain, and generates an electric field to stimulate contraction. The intended output of the device is the controlled culture of a minimal functional unit of skeletal muscle that surpasses current standards of in vitro and in vivo pre-clinical models

2020 Huskies Showcase Abstracts

The 2020 Huskies Showcase abstracts are arranged in the following order: Applied Experience Displays; Artistic Performances; Demonstrations; Gallery Exhibits; Oral Presentations; Poster Presentations

CIR-Myo News: Abstracts of the 2015 Spring Padua Muscle Days

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Exploring protein fitness landscapes with new high-throughput technologies

The concept of a protein’s fitness landscape – an abstract space in which related sequences are close together and matched with their fitness – is a useful tool to visualize core principles of protein evolution. Acquiring a new function, for example the laboratory evolution of an enzyme to convert an industrially relevant substrate, can be understood as a stepwise climb through a fitness landscape, reaching higher fitness (or activity) with each step (or mutation). The valleys of such a space relate to the starting points of protein engineering campaigns. Understanding this area could enlighten principles of how proteins quickly adapt in nature and help to identify starting points with a high potential for evolution, a high ‘evolvability’, speeding up protein engineering. In this study, high-throughput technologies will be developed that enable the read-out of directed evolution on a large scale, tracking the exploration of the valley of a fitness landscape: the conversion of an amino acid- to amine dehydrogenase will be investigated as a model of enzyme evolvability with a drastic change of substrate specificity. A sensitive high-throughput screening assay as well as a comprehensive sequencing read-out will be required to establish the identity of selected variants during evolution. I will first generate and characterize three different but related starting points and test their initial evolvability. Stabilizing the starting point results in increased mutational robustness, broadening the range of accepted mutations. However, increased initial stability does not necessarily correlate to higher functional improvement, hinting at a nuanced view of evolvability. A sensitive high-throughput assay is necessary to verify the full potential of the starting points and study the early steps of evolution comprehensively. Broadly applicable ultrahigh-throughput assays of enzyme function, such as absorbance-activated droplet sorting, currently lack the sensitivity of more specific fluorescence-based or low-throughput counterparts. A universal approach to increase detectability in single cell-lysate microfluidic enzyme assays is established by amplifying the enzyme content per droplet more than 10-fold via homogeneous clonal cell growth. Clonal amplification enables the sensitive and precise detection of newly introduced amine dehydrogenase activities, a feat restricted in conventional assays by low initial activity and stability. To generate a truly complete view of directed evolution in a fitness landscape, however, an equally powerful sequencing read-out is necessary to identify all selected variants. Here, unique molecular identifiers are used to increase the accuracy of nanopore sequencing to levels that can reliably distinguish point mutations. I establish an inexpensive and straightforward long read amplicon sequencing workflow which is then applied to map the trajectories of two comparative long-term directed evolution campaigns. In the parallel evolution campaigns, initial beneficial mutations are exclusive to each starting point and lead to incompatible trajectories. Beneficial mutations are scarce and large improvements are unavailable until recombination occurs and a jump through the fitness landscape is realized. The recombined variant holds high evolvability and quickly evolves to take over the population and form the most successful lineages, indicating the power of recombination as a means to innovation in protein evolution. The tools established in this thesis can help protein engineers explore fitness landscapes more economically and comprehensively. Their application to mapping full trajectories of early adaptation uncovers differences in the evolvability of homologs, potentially aiding the identification of evolvable starting points as well as strategies to increase evolvability for efficient protein engineering in the future

2013 Oklahoma Research Day Full Program

This document contains all abstracts from the 2013 Oklahoma Research Day held at the University of Central Oklahoma

How to build a biological machine using engineering materials and methods

We present work in 3D printing electric motors from basic materials as the key to building a self-replicating machine to colonise the Moon. First, we explore the nature of the biological realm to ascertain its essence, particularly in relation to the origin of life when the inanimate became animate. We take an expansive view of this to ascertain parallels between the biological and the manufactured worlds. Life must have emerged from the available raw material on Earth and, similarly, a self-replicating machine must exploit and leverage the available resources on the Moon. We then examine these lessons to explore the construction of a self-replicating machine using a universal constructor. It is through the universal constructor that the actuator emerges as critical. We propose that 3D printing constitutes an analogue of the biological ribosome and that 3D printing may constitute a universal construction mechanism. Following a description of our progress in 3D printing motors, we suggest that this engineering effort can inform biology, that motors are a key facet of living organisms and illustrate the importance of motors in biology viewed from the perspective of engineering (in the Feynman spirit of "what I cannot create, I cannot understand")