The overall goal of the Cell & Molecular Imaging (CMI) Shared Resource is to provide MUSC Hollings Cancer Center members with sophisticated equipment, technologies, training, and expertise required for successful, state-of-the-art cell and tissue-based microscopic imaging and image analysis.

CMI carries out activities under three major themes:

Optical Microscopy Services: CMI maintains an array of contemporary equipment and expertise to facilitate high-end imaging of tissues and cells by Hollings members.
Innovative Techniques: CMI develops and applies new imaging techniques and applications to meet the emerging scientific needs of Hollings members.
Education and Training: CMI educates, trains, and consults on sophisticated imaging technologies that enable scientific discovery, including a biennial Charleston Workshop on Light Microscopy for the Biomedical Sciences, as well as a lecture series on cell and molecular imaging, especially as it relates to tumor biology.
Schedule Use

The MUSC Mass Spectrometry Facility, housed within the Proteomics Center, provides expertise, services, education, and state-of-the-art instrumentation to enhance biomedical research through proteomics and metabolomics. High resolution, accurate mass (HR/AM) mass spectrometers are available for protein identification, characterization of post-translational modifications, protein profiling, identification of protein interactions and drug targets, and biomarker discovery. The core also assists in the development of customized isolation, detection, and characterization of post-translationally modified peptides.
Targeted metabolomics and lipidomics profiling is available using Biocrates MxP Quant 500/500XL, MxP Quant 1000, or AbsoluteIDQ p180 platforms.

Equipment and Computing Infrastructure: Quantitative proteomic experiments (LFQ, nDIA, TMT, SILAC, IS-PRM) can be performed on the Thermo Scientific Vanquish Neo UHPLC Orbitrap Astral Zoom LC-MS/MS with Biopharma and Faims; Easy 1200 nanoLC-Orbitrap Exploris 480 LC-MS/MS; or Easy 1200 nanoLC Orbitrap Fusion Lumos LC-MS/MS with CID, HCD, ETD, EThcD, and UVPD (213 nm) fragmentation capabilities. For sample preparation a Kingfisher Apex, Opentrons OT-2, and Thermo Scientific Vanquish UPLC with diode array detector are available. Software platforms available include MaxQuant, Spectronaut 20, Proteome Discoverer 3.3 with Chimerys, Biopharma Finder, Fragpipe, and Skyline. For database searches a 6 x Intel Xeon Gold 6238R processor (28 cores 56 threads 2.2 GHz up to 4 GHz) with 48GB RAM or a 2 x Intel Xeon E5-2695 processor (18 cores 36 threads 2.1 GHz up to 3.3 GHz) with 128GB RAM are available. For Orbitrap Astral data, the Ardia Platform Server: Dell PowerEdge T550: 2 x Intel Xeon Platinum 8352M processor (64 cores 128 threads 2.3 GHz with 512GB RAM) and Precision 7960 Tower XCTO Base: Intel Xeon w9-3495X (105MB Cache, 56 cores, 112 threads, 1.9GHz to 4.8GHz) are available. Statistical and bioinformatic analyses are performed with Perseus (Max Planck Institute), Graphpad Prism, as well as R-packages from Bioconductor. Raw data are temporarily stored on high-speed servers with automated backup and deposited upon request in the PRIDE repository via the ProteomeXchange consortium. Targeted, absolute quantification of metabolites using the Biocrates platform is available on the Thermo Scientific Vanquish Flex UPLC-TSQ Altis Plus MS and Vanquish Horizon HPLC-Exploris 480 MS. Software used for metabolomic analysis include WebIDQ, Compound Discoverer, Skyline, and MetaboAnalyst.

The Medical University of South Carolina (MUSC) Gnotobiotic Animal Core offers investigators a unique opportunity to assess the impact of host microbiome interactions on human health and disease. The Core provides the physical and intellectual resources associated with the generation, care, and use of germ-free, defined microbiota, and conventionalized mice. Core services are available to scientists at academic institutions, biotechnology companies, and large pharmaceutical corporations.

As a cost center, all services provided by the MUSC Gnotobiotic Animal Core are on a fee-for-service basis. Please contact the Core Director to inquire about services and current rates.

Understanding the complexities of redox mediated signaling events requires a multidisciplinary approach. The SC COBRE in Oxidants, Redox Balance and Stress Signalling has assembled a cohort of promising junior faculty with expertise in relevant biomedical model systems. Analytical biochemistry specific to the detection and quantification of redox sensitive molecules and coordinate protein changes that drive homeostasis is a unique niche fulfilled by the Analytical Redox Biology Core (ARBC).

The primary objective of the Core is to provide comprehensive analytical redox biochemistry methods and mentoring support for the COBRE junior faculty with the goal to advance their research endeavors, publications and fundability. The specific aims of the ARBC are: 1) Provide ROS /RNS identification and quantification using state-of-the-art techniques; 2) Perform quantitative analysis of ROS/RNS (redox molecules and metabolites), including those associated with calcium mobilization and changes in energy metabolism; 3) Provide expertise and technology for in depth biochemical analysis of thiol-centered enzyme activities and define protein:protein interactions.

Since oxidative (nitrosative) stress often is associated with a conditional increase in antioxidant protection, the Core has established methods to detect and measure various antioxidant enzyme activities as a function of oxidant stress/antioxidant protection equilibrium. Comprehensive analysis of redox status also includes measurement of intracellular GSH, GSSG, protein surface and “buried” thiols utilizing both endpoint and/ or real-time kinetic measurements with millisecond resolution. In complex studies of redox signaling, certain protein:protein interactions appear to be redox dependent and attributed to post-translational modifications, including S-nitrosylation and S-glutathionylation. The ARBC has developed fluorescent labeling and FRET analysis to evaluate redox dependent protein:protein interactions with subsequent in silico molecular modeling using ZDOCK, GOLD Suite (v 5.2) software. Collectively, these technologies will provide a multidisciplinary approach to advance the understanding of redox mediated signaling events specific to the model systems presented by the junior faculty in their research.

Cellular redox species are produced directly or indirectly via bioenergetic metabolic reactions. Although the leak of electrons is often cited as the primary source of superoxide and hydroxy radicals, the leak is only a small contributor to the many different species involved in cellular redox reactions. Indeed, the fundamental basis of bioenergetics involves the oxidation (loss of electrons) of reduced nutrients and subsequent production of metabolites with a range of redox potentials (i.e., nicotinamides, reduced/oxidized metalloproteins, and thiol-containing species with varied redox potentials. Profiling the flux of these various metabolites through their attendant metabolic reactions is fundamental to any studies aimed at understanding cellular redox reactions.

The Bioenergetics Core provides several of the leading technologies that enable researchers to quantify the fluxes of these metabolic reactions in cells, tissues, organoids and small animal models such as zebrafish embryos and nematodes. The central technologies include high resolution respirometry using the XF technology from Seahorse Biosciences/Agilent. Dr. Beeson was involved in the original design of the XF technology profiles extracellular fluxes of oxygen, lactate and CO2 as the samples are interrogated with pharmacological and/or genetic manipulations. The instrumentation utilizes 96-well microplates to provide sufficient sample numbers to provide robust, statistically validated flux profiles of glycolysis, mitochondrial respiration, fatty acid oxidation, glutamine utilization and other related metabolic processes. Rapid, high-throughput imaging optimized to the XF plate architecture provides normalization of cell/tissue numbers, health, and other.

Isotopomer analyses of Krebs cycle intermediates and their byproducts utilizes LC-GC/MS. Typical 13C-labels at particular positions of, for example glucose, are introduced to cells or tissue small samples are periodically quenched, lysed and derivatized to volatile esters. The key advantage is that only the low molecular weight acids readily enter the gas phase for analyses that enable determination of enrichment of the 13C at positions that reveal the fluxes through specific pathways and/or the conversions to key species such as 2-hydroxy-glutamic acid – and oncometabolite produced by a mutated form of isocitrate dehydrogenase seen in many tumors that have escaped from therapeutic pressures. The oncometabolites affect epigenetic mechanisms that regulate tumor cell growth and proliferation.

A key feature of the core is that Dr. Beeson and his team also provide extensive training, data analyses support and aid in experimental design – it is fundamentally a collaborative unit.

Lab produces purified proteins on a large scale to support research activities at MUSC and outside customers. The lab also contains equipment for biophysical characterization of proteins, including ITC, circular dichroism and dynamic light scattering

The COBRE Mass Spectrometry Core is housed within the MUSC Mass Spectrometry Facility which provides expertise, services, education, and training to enhance biomedical research endeavors through mass spectrometry-based proteomics. Currently there are over 50 investigators which utilize the facility for protein identification and characterization. Protein analysis includes in-gel or in-solution protease digestion, chromatographic separation and tandem mass spectrometric analysis of the resulting peptides, and interpretation of MS/MS data using Sequest , Mascot, Protein Pilot, MaxQuant, and other search algorithms. The facility also assists in the development of customized applications for the isolation, detection and characterization of posttranslationally modified peptides (e.g. phosphorylation, glycosylation, oxidation, glutathionylation, and O-GlcNAc modification). With the recent acquisition of the Orbitrap Elite Mass Spectrometer we are expanding our services to couple quantitative approaches (SILAC, iTRAQ®, ICAT®, TMT®) to modification-specific experiments (eg., phosphoproteomics, redox proteomics). We are developing methodology to analyze alterations in posttranslational regulation that impact signal transduction, epigenetic modulation, and the response to therapeutics with the goal of enabling investigators to discover molecular mechanisms underlying disease progression and therapeutic responses that may not be revealed through genomic studies.