Uptake of nonesterified long-chain fatty acids (LCFAs) into many cell types and organs such as liver, heart, intestine, and skeletal muscle occurs primarily through a saturable, protein-mediated mechanism. Membrane proteins that increase the uptake of LCFAs, such as FAT/CD36 and fatty acid transport proteins, represent significant therapeutic targets for the treatment of metabolic disorders, including type 2 diabetes. However, currently available methods for the quantification of LCFA uptake neither allow for real-time measurements of uptake kinetics nor are ideally suited for the development of LCFA uptake inhibitors in high-throughput screens. To address both problems, we developed a LCFA uptake assay using a fluorescently labeled fatty acid and a nontoxic cell-impermeable quenching agent that allows fatty acid transport to be measured in real time using fluorescence plate readers or standard fluorescence microscopy. With this assay, we faithfully reproduced known differentiationand hormone-induced changes in LCFA uptake by 3T3-L1 cells and determined LCFA uptake kinetics with previously unobtainable temporal resolution.Applications of this novel assay should facilitate new insights into the biology of fatty acid uptake and provide new means for obesity-related drug discovery. -Liao, J., R. Sportsman, J. Harris, and A. Stahl. Real-time quantification of fatty acid uptake using a novel fluorescence assay. J. Lipid Res. 2005. 46: 597-602.Supplementary key words long-chain fatty acids • fatty acid uptake assay • quencher dyes Uptake of long-chain fatty acids (LCFAs) plays an important role in the absorption of dietary lipids as well as the delivery of metabolic energy to a variety of tissues. Besides their function as substrates for ␤ -oxidation, fatty acids also contribute to membrane synthesis, protein modifications, immune responses, and activation of protein kinases and nuclear hormone receptors (1, 2). Recent findings have also directly implicated increased intracellular levels of LCFAs in the obesity-associated insulin desensitization of skeletal muscle and liver (1, 3).LCFA uptake in adipocytes is mainly facilitated by membrane proteins, particularly members of the fatty acid transport protein (FATPs/SLC27) family. Mammalian genomes have been shown to contain six FATP genes (4). The identification of this fatty acid transporter family and other fatty acid uptake-enhancing proteins such as CD36 has allowed a better understanding of the mechanisms and regulation of LCFA transport on a cellular level, yielding insight into the control of energy homeostasis and its dysregulation in diseases such as diabetes and obesity. In addition, these cell surface proteins represent new targets for the inhibition of LCFA uptake.To gain a better understanding of the molecular dynamics of fatty acid uptake and the development of small molecular inhibitors of this process, robust and physiologically relevant measurements of LCFA uptake kinetics are required. Here, we report the development of a fluorescence assay bas...

A monoclonal antibody, selected for reactivity with the Epstein-

Using the components of a particularly well-studied plant virus, cowpea chlorotic mottle virus (CCMV), we demonstrate the synthesis of virus-like particles (VLPs) with one end of the packaged RNA extending out of the capsid and into the surrounding solution. This construct breaks the otherwise perfect symmetry of the capsid and provides a straightforward route for monofunctionalizing VLPs using the principles of DNA nanotechnology. It also allows physical manipulation of the packaged RNA, a previously inaccessible part of the viral architecture. Our synthesis does not involve covalent chemistry of any kind; rather, we trigger capsid assembly on a scaffold of viral RNA that is hybridized at one end to a complementary DNA strand. Interaction of CCMV capsid protein with this RNA-DNA template leads to selective packaging of the RNA portion into a well-formed capsid, but leaves the hybridized portion poking out of the capsid through a small hole. We show that the RNA-DNA protruding from the capsid is capable of binding DNA and DNA-functionalized colloidal particles. Additionally, we show that the RNA-DNA scaffold can be used to nucleate virus formation on a DNA-functionalized surface. We believe this self-assembly strategy can be adapted to viruses other than CCMV.

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of DNA. Typically, acetylation of histone tails leads to gene activation associated with a loosely folded chromatin structure. Conversely, tri-methylation of histone tails and methylation of DNA lead to gene repression associated with a compacted structure of the chromatin. Despite decades-long efforts, the microscopic mechanism of epigenetic marker-mediated modulation of chromatin structure remains unknown. A possible explanation is the action of ''effector'' proteins that read epigenetic markers and alter DNA-DNA interactions depending on the message carried by the markers. However, none of the ''effector'' protein candidates characterized thus far can account for the observed chromatin compaction phenomena. Here, we combine molecular dynamics simulations with single-molecule FRET experiments to demonstrate modulation of DNA-DNA interactions by epigenetic markers that does not involving any of the ''effector'' proteins. In our MD simulations, we found that tri-methylations of histone tails and methylation of DNA cooperatively strengthen the histone-tail-mediated DNA-DNA association by increasing the number of lysine residues bridging the DNA molecules. Single-molecule FRET experiments confirmed the predictions of the molecular dynamics simulations. Our effector-free chromatin condensation mechanism suggests that epigenetic markers not only serve as information carriers but also can physically affect interactions between the DNA molecules.

The structure of the 5 0 -Leader (5 0 -L) of the human immunodeficiency virus (HIV-1) viral RNA genome is under intense study, due to its role in determining the fate of the RNA. Within the host cell, the 5 0 -L is in equilibrium between a monomeric and dimeric conformation. The monomer is translated

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