Information Security Framework for Small and Medium Sized Businesses

2006-05-19 (Removed from collection 2006-11-21) Revised version reinstated 2009-06-17Information security issues are a challenge to everyone who uses computers. The rise of the personal computer as a common business tool and the Internet as a common means of business communication and commerce have also created an environment that criminals with technical knowledge can exploit to prey upon the less technically savvy. The cost of computer crime to business in the United States has risen to $67 billion according to the 2005 FBI Computer Crime Survey. Not a day goes by that a computer security exploit or identity theft scheme makes national headlines. The impact to small and medium sized businesses is tremendous. These businesses have the least amount of resources to use to help defend against hacker attacks and they suffer some of the largest net financial impacts when victimized by an attack. The good news is that there are some simple things a business owner can do to greatly reduce the risks of being victimized by an information security failure. Education and awareness of the most prevalent risks to business information and commonly exploited security holes can quickly close the door to a security incident. Just as with traditional burglary attempts, the computer criminals will first look for the path of least resistance when trying to break in to a computer system. If a door is unlocked, all the criminal has to do is walk right in. The problem with computer technology is that many people do not even know when the doors are unlocked. By raising awareness of the most common vectors of attacks against business computer systems, this field project seeks to help business owners better manage and protect their information assets. The computer risks and mitigation approaches outlined in this project will not completely eliminate all the computer security exposures that company can face in the 21st century business environment but they will help a business owner know what they can do to quickly reduce their risk exposure. Just like with any other type of crime, a determined criminal may eventually find some type of security weakness that can be exploited for illicit purposes. The goal of the business owner is to make the criminal’s work so hard that they look elsewhere to commit their crimes

Improving reservoir conformance using gelled polymer systems. Final report, September 25, 1992--July 31, 1996

The objectives of the research program were to (1) identify and develop polymer systems which have potential to improve reservoir conformance of fluid displacement processes, (2) determine the performance of these systems in bulk and in porous media, and (3) develop methods to predict their performance in field applications. The research focused on four types of gel systems--KUSP1 systems that contain an aqueous polysaccharide designated KUSP1, phenolic-aldehyde systems composed of resorcinol and formaldehyde, colloidal-dispersion systems composed of polyacrylamide and aluminum citrate, and a chromium-based system where polyacrylamide is crosslinked by chromium(III). Gelation behavior of the resorcinol-formaldehyde systems and the KUSP1-borate system was examined. Size distributions of aggregates that form in the polyacrylamide-aluminum colloidal-dispersion gel system were determined. Permeabilities to brine of several rock materials were significantly reduced by gel treatments using the KUSP1 polymer-ester (monoethyl phthalate) system, the KUSP1 polymer-boric acid system, and the sulfomethylated resorcinol-formaldehyde system were also shown to significantly reduce the permeability to supercritical carbon dioxide. A mathematical model was developed to simulate the behavior of a chromium redox-polyacrylamide gel system that is injected through a wellbore into a multi-layer reservoir in which crossflow between layers is allowed. The model describes gelation kinetics and filtration of pre-gel aggregates in the reservoir. Studies using the model demonstrated the effect filtration of gel aggregates has on the placement of gel systems in layered reservoirs

Improved Oil Recovery in Fluvial Dominated Deltaic Reservoirs of Kansas Near Term

The objective of this project is to address waterflood problems of the type found in Morrow sandstone reservoirs in southwestern Kansas and Cherokee Group reservoirs in southeastern Kansas. Two demonstration sites operated by different independent oil operators are involved in this project. The Stewart Field is located in Finney County, Kansas and is operated by North American Resources Company. The Nelson Lease is located in Allen County, Kansas, in the N.E. Savonburg Field and is operated by James E. Russell Petroleum, Inc. General topics to be addressed are (1) reservoir management and performance evaluation, (2) waterflood optimization, and (3) the demonstration of recovery processes involving off-the-shelf technologies which can be used to enhance waterflood recovery, increase reserves, and reduce the abandonment rate of these reservoir types. In the Stewart Project, the reservoir management portion of the project conducted during Budget Period I involved performance evaluation. This included (1) reservoir characterization and the development of a reservoir database, (2) volumetric analysis to evaluate production performance, (3) reservoir modeling, (4) laboratory work, (5) identification of operational problems, (6) identification of unrecovered mobile oil and estimation of recovery factors, and (7) identification of the most efficient and economical recovery process. To accomplish these objectives the initial budget period was subdivided into three major tasks. The tasks were (1) geological and engineering analysis, (2) laboratory testing, and (3) unitization. Due to the presence of different operators within the field, it was necessary to unitize the field in order to demonstrate a field-wide improved recovery process. This work was completed and the project moved into Budget Period 2. Budget Period 2 objectives consisted of the design, construction, and operation of a field-wide waterflood utilizing state-of-the-art, off-the-shelf technologies in an attempt to optimize secondary oil recovery. To accomplish these objectives the second budget period was subdivided into five major tasks. The tasks were (1) design and construction of a waterflood plant, (2) design and construction of a water injection system, (3) design and construction of tank battery consolidation and gathering system, (4) initiation of waterflood operations and reservoir management, and (5) technology transfer. In the Savonburg Project, the reservoir management portion involves performance evaluation. This work included (1) reservoir characterization and the development of a reservoir database, (2) identification of operational problems, (3) identification of near wellbore problems such as plugging caused from poor water quality, (4) identification of unrecovered mobile oil and estimation of recovery factors, and (5) preliminary identification of the most efficient and economical recovery process i.e., polymer augmented waterflooding or infill drilling (vertical or horizontal wells). To accomplish this work the initial budget period was subdivided into four major tasks. The tasks included (1) geological and engineering analysis, (2) waterplant optimization, (3) wellbore cleanup and pattern changes, and (4) field operations. This work was completed and the project has moved into Budget Period 2. The Budget Period 2 objectives consisted of continual optimization of this mature waterflood in an attempt to optimize secondary and tertiary oil recovery. To accomplish these objectives the second budget period was subdivided into six major tasks. The tasks were (1) waterplant development, (2) profile modification treatments, (3) pattern changes, new wells and wellbore cleanups, (4) reservoir development (polymer flooding), (5) field operations, and (6) technology transfer

Improved oil recovery in fluvial dominated reservoirs of Kansas--near-term. Annual report

Common oil field problems exist in fluvial dominated deltaic reservoirs in Kansas. The problems are poor waterflood sweep efficiency and lack of reservoir management. The poor waterflood sweep efficiency is due to (1) reservoir heterogeneity, (2) channeling of injected water through high permeability zones or fractures, and (3) clogging of injection wells due to solids in the injection water. In many instances the lack of reservoir management results from (1) poor data collection and organization, (2) little or no integrated analysis of existing data by geological and engineering personnel, (3) the presence of multiple operators within the field, and (4) not identifying optimum recovery techniques. Two demonstration sites operated by different independent oil operators are involved in this project. The Stewart Field is located in Finney County, Kansas and is operated by North American Resources Company. This field was in the latter stage of primary production at the beginning of this project and is currently being waterflooded as a result of this project. The Nelson Lease (an existing waterflood) is located in Allen County, Kansas, in the N.E. Savonburg Field and is operated by James E. Russell Petroleum, Inc. The objective is to increase recovery efficiency and economics in these type of reservoirs. The technologies being applied to increase waterflood sweep efficiency are (1) in situ permeability modification treatments, (2) infill drilling, (3) pattern changes, and (4) air flotation to improve water quality. The technologies being applied to improve reservoir management are (1) database development, (2) reservoir simulation, (3) transient testing, (4) database management and (5) integrated geological and engineering analysis. Results of these two field projects are discussed

Mild/moderate haemophilia A: new insights into molecular mechanisms and inhibitor development

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/72987/1/j.1365-2516.2008.01730.x.pd

A Novel Genetic Screen Implicates Elm1 in the Inactivation of the Yeast Transcription Factor SBF

BACKGROUND: Despite extensive large scale analyses of expression and protein-protein interactions (PPI) in the model organism Saccharomyces cerevisiae, over a thousand yeast genes remain uncharacterized. We have developed a novel strategy in yeast that directly combines genetics with proteomics in the same screen to assign function to proteins based on the observation of genetic perturbations of sentinel protein interactions (GePPI). As proof of principle of the GePPI screen, we applied it to identify proteins involved in the regulation of an important yeast cell cycle transcription factor, SBF that activates gene expression during G1 and S phase. METHODOLOGY/PRINCIPLE FINDINGS: The principle of GePPI is that if a protein is involved in a pathway of interest, deletion of the corresponding gene will result in perturbation of sentinel PPIs that report on the activity of the pathway. We created a fluorescent protein-fragment complementation assay (PCA) to detect the interaction between Cdc28 and Swi4, which leads to the inactivation of SBF. The PCA signal was quantified by microscopy and image analysis in deletion strains corresponding to 25 candidate genes that are periodically expressed during the cell cycle and are substrates of Cdc28. We showed that the serine-threonine kinase Elm1 plays a role in the inactivation of SBF and that phosphorylation of Elm1 by Cdc28 may be a mechanism to inactivate Elm1 upon completion of mitosis. CONCLUSIONS/SIGNIFICANCE: Our findings demonstrate that GePPI is an effective strategy to directly link proteins of known or unknown function to a specific biological pathway of interest. The ease in generating PCA assays for any protein interaction and the availability of the yeast deletion strain collection allows GePPI to be applied to any cellular network. In addition, the high degree of conservation between yeast and mammalian proteins and pathways suggest GePPI could be used to generate insight into human disease

The yeast P5 type ATPase, Spf1, regulates manganese transport into the endoplasmic reticulum

The endoplasmic reticulum (ER) is a large, multifunctional and essential organelle. Despite intense research, the function of more than a third of ER proteins remains unknown even in the well-studied model organism Saccharomyces cerevisiae. One such protein is Spf1, which is a highly conserved, ER localized, putative P-type ATPase. Deletion of SPF1 causes a wide variety of phenotypes including severe ER stress suggesting that this protein is essential for the normal function of the ER. The closest homologue of Spf1 is the vacuolar P-type ATPase Ypk9 that influences Mn2+ homeostasis. However in vitro reconstitution assays with Spf1 have not yielded insight into its transport specificity. Here we took an in vivo approach to detect the direct and indirect effects of deleting SPF1. We found a specific reduction in the luminal concentration of Mn2+ in ∆spf1 cells and an increase following it’s overexpression. In agreement with the observed loss of luminal Mn2+ we could observe concurrent reduction in many Mn2+-related process in the ER lumen. Conversely, cytosolic Mn2+-dependent processes were increased. Together, these data support a role for Spf1p in Mn2+ transport in the cell. We also demonstrate that the human sequence homologue, ATP13A1, is a functionally conserved orthologue. Since ATP13A1 is highly expressed in developing neuronal tissues and in the brain, this should help in the study of Mn2+-dependent neurological disorders

HcRed, a Genetically Encoded Fluorescent Binary Cross-Linking Agent for Cross-Linking of Mitochondrial ATP Synthase in Saccharomyces cerevisiae

Genetically encoded fluorescent cross-linking agents represent powerful tools useful both for visualising and modulating protein interactions in living cells. The far-red fluorescent protein HcRed, which is fluorescent only in a dimer form, can be used to promote the homo-dimerisation of target proteins, and thereby yield useful information about biological processes. We have in yeast cells expressed HcRed fused to a subunit of mitochondrial ATP synthase (mtATPase). This resulted in cross-linking of the large multi-subunit mtATPase complex within the inner-membrane of the mitochondrion. Fluorescence microscopy revealed aberrant mitochondrial morphology, and mtATPase complexes isolated from mitochondria were recovered as fluorescent dimers under conditions where complexes from control mitochondria were recovered as monomers. When viewed by electron microscopy normal cristae were absent from mitochondria in cells in which mATPase complexes were cross-linked. mtATPase dimers are believed to be the building blocks that are assembled into supramolecular mtATPase ribbons that promote the formation of mitochondrial cristae. We propose that HcRed cross-links mATPase complexes in the mitochondrial membrane hindering the normal assembly/disassembly of the supramolecular forms of mtATPase

Human Cell Chips: Adapting DNA Microarray Spotting Technology to Cell-Based Imaging Assays

Here we describe human spotted cell chips, a technology for determining cellular state across arrays of cells subjected to chemical or genetic perturbation. Cells are grown and treated under standard tissue culture conditions before being fixed and printed onto replicate glass slides, effectively decoupling the experimental conditions from the assay technique. Each slide is then probed using immunofluorescence or other optical reporter and assayed by automated microscopy. We show potential applications of the cell chip by assaying HeLa and A549 samples for changes in target protein abundance (of the dsRNA-activated protein kinase PKR), subcellular localization (nuclear translocation of NFκB) and activation state (phosphorylation of STAT1 and of the p38 and JNK stress kinases) in response to treatment by several chemical effectors (anisomycin, TNFα, and interferon), and we demonstrate scalability by printing a chip with ∼4,700 discrete samples of HeLa cells. Coupling this technology to high-throughput methods for culturing and treating cell lines could enable researchers to examine the impact of exogenous effectors on the same population of experimentally treated cells across multiple reporter targets potentially representing a variety of molecular systems, thus producing a highly multiplexed dataset with minimized experimental variance and at reduced reagent cost compared to alternative techniques. The ability to prepare and store chips also allows researchers to follow up on observations gleaned from initial screens with maximal repeatability

Use of cDNA Tiling Arrays for Identifying Protein Interactions Selected by In Vitro Display Technologies

In vitro display technologies such as mRNA display are powerful screening tools for protein interaction analysis, but the final cloning and sequencing processes represent a bottleneck, resulting in many false negatives. Here we describe an application of tiling array technology to identify specifically binding proteins selected with the in vitro virus (IVV) mRNA display technology. We constructed transcription-factor tiling (TFT) arrays containing ∼1,600 open reading frame sequences of known and predicted mouse transcription-regulatory factors (334,372 oligonucleotides, 50-mer in length) to analyze cDNA fragments from mRNA-display screening for Jun-associated proteins. The use of the TFT arrays greatly increased the coverage of known Jun-interactors to 28% (from 14% with the cloning and sequencing approach), without reducing the accuracy (∼75%). This method could detect even targets with extremely low expression levels (less than a single mRNA copy per cell in whole brain tissue). This highly sensitive and reliable method should be useful for high-throughput protein interaction analysis on a genome-wide scale