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<h1 class="titleblock__title" id="title">NIH Announces Follow that Cell Challenge Finalists</h1>
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<time class="pagestamp_news_time" datetime="2015-03-16">March 16, 2015</time>
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<html><body><p><iframe width="460" height="259" src="https://www.youtube.com/embed/lwvsvIPZLUI?rel=0" frameborder="0" allowfullscreen="allowfullscreen"></iframe></p><p>The National Institutes of Health has selected 16 finalists for Phase 1 of its <a href="http://commonfund.nih.gov/singlecell/challenge" rel="external">Follow that Cell Challenge <i class="fa-solid fa-arrow-up-right-from-square ext-link-icon"></i></a>. The goal of the challenge is to stimulate the development of new tools and methods that will enable researchers to predict the behavior and function of a single cell in complex tissue over time. This ability could help reveal valuable information such as how cells transition from a healthy to diseased state, or identify changes that influence a cell’s responsiveness to treatment. In addition, non-destructive methods for monitoring single cells could assist with early disease detection and allow doctors to better tailor therapies to cells as they evolve throughout the course of a disease.</p><p>During Phase 1 of the challenge, innovators across a wide range of fields were encouraged to propose theoretical solutions for tracking and analyzing the behavior and function of individual cells over a period of minutes, hours, and even days. Of the 16 finalists, five prize winners were selected to receive monetary prizes totaling $88,000 and will now advance—along with the additional 11 finalists—to the challenge’s second phase, which requires innovators to generate proof-of-concept data.</p><p>“This is the first challenge of this magnitude, not just for the NIH Common Fund, but for the NIH in general. The challenge seeks to stimulate novel approaches to probing individual cell behavior and function over time, which can lead to fundamental new insights into disease processes and, eventually, treatments,” said James M. Anderson, M.D., Ph.D., director of the NIH’s Division of Program Coordination, Planning, and Strategic Initiatives, which houses the NIH Common Fund. “Through the unique challenge mechanism, we hope to tap into investigators’ ideas not typically reached through traditional avenues of NIH funding. Based on the intriguing and innovative solutions proposed by the phase 1 finalists, this seems to be true. We look forward to what will be achieved through phase two of the challenge.”</p><p>Phase 1 solutions were submitted last December by individuals or teams. The Follow that Cell Challenge is part of the America COMPETES initiative and was issued by the National Institute of Mental Health (NIMH) and the National Institute of Biomedical Imaging and Bioengineering (NIBIB), on behalf of the NIH Common Fund’s Single Cell Analysis Program. The submissions were evaluated by scientific experts from across the NIH and then reviewed by a three-judge panel.</p><p>“The large number of highly novel solutions that were proposed underlines the benefits of reaching out to innovators across many different fields. There is tremendous power in merging concepts and expertise from engineering, chemistry, and molecular biology to solve challenging issues in biomedical research. These innovative solutions are a prime example of that power,” said Roderic Pettigrew, Ph.D., M.D., director of NIBIB. “The successful development of any of the selected projects would have a very large impact on our understanding of health and disease states. We are eager for each to be carried forward.”</p><p>“Like the BRAIN Initiative grants we awarded last Fall, these projects represent the best of ‘out-of-the-box’ thinking by some of the most talented minds in the field,” added NIMH director Thomas R. Insel, M.D.</p><p>Phase 2 begins on March 17, 2015 and is open only to the 16 finalists. During Phase 2, Reduction to Practice, finalists will generate proof-of-concept data related to their Phase 1 entries. These submissions are due March 30, 2017. Winners of Phase 2 will be awarded prize money from a pool of $400,000, to be announced July 31, 2017.</p><p>The Phase 1 prize winners will be presented and recognized as part of the 3rd Annual Single Cell Analysis Investigators Meeting, which is scheduled for April 20-21, 2015 at the Natcher Conference Center on the NIH Campus in Bethesda, Maryland.</p><p>Although final verification of eligibility is still pending, a list of proposed finalists and brief descriptions of the five prize-winning solutions can be found below. For more information about these projects and descriptions of all the finalists’ projects, please visit the <a href="http://commonfund.nih.gov/Singlecell" rel="external">Single Cell Analysis Program website <i class="fa-solid fa-arrow-up-right-from-square ext-link-icon"></i></a>.</p><p>FIRST PLACE PRIZE WINNER:</p><p><strong>Single cell timelapse gene expression profiling via an engineered self-reporting pathway</strong></p><p>Paul Blainey, Ph.D. (team lead), MIT and Broad Institute, Cambridge, Massachusetts<br>The researchers propose to engineer an RNA export pathway that can capture a small amount of a cell’s mRNA, label it with a unique barcode, and then secrete it out of the cell. The secreted mRNA can then be collected from the extracellular environment and analyzed at different time points to determine how gene expression in one cell changes over time. The technique is integrated with microscopic imaging so that the changes in the cell’s gene expression can be correlated with changes in its phenotype.</p><p>ADDITIONAL PRIZE WINNERS:</p><p><strong>Self-destructing cellular barcode: a versatile tool for single cell analysis</strong></p><p>James Ankrum, Ph.D., University of Iowa, Iowa City, Iowa</p><p>Of critical importance for studying single cell activity is the ability to identify and track a single cell over time. This solution proposes a method for uniquely labelling thousands of single cells. The proposed label lasts for several weeks, is transferred to cell progeny, and self-destructs when the cell dies. The technique would be useful for determining stem cell fate and lineage.</p><p><strong>Measuring protein concentrations and protein translation over time in single cells </strong><em><strong>in vivo</strong></em></p><p>Brian Chen, Ph.D., McGill University, Montréal, Québec</p><p>The amount of protein that a cell produces is tightly regulated; too little or too much of a single protein can lead to disease. The ability to understand how protein production affects cell phenotype is an important step in understanding how diseases occur. This solution proposes to develop a technique for tracking and measuring protein production in single cells of living animals. Such a technique would permit researchers to measure real-time changes of protein production within a cell’s native environment at unprecedented resolution.</p><p><strong>BLINKER assessed live cell transcriptomics</strong></p><p>James Eberwine, Ph.D., (team lead), University of Pennsylvania, Philadelphia, Pennsylvania</p><p>This solution proposes the development of a sensor called Blinker to visualize the transcription of genes in real time in live neurons. The sensor is comprised of a peptide that produces a detectable flash when bound to a specific sequence on a newly transcribed mRNA molecule. For any given mRNA molecule, the distance between flashes will be different and this unique pattern can be used to identify the gene that is being expressed. The ability to visualize and identify the synthesis of many mRNA molecules over a period of minutes could yield important information about which genes are important during long-term potentiation and how the expression of certain genes affects the responsiveness of neurons to drugs.</p><p><strong>Study the longitudinal expression of the genome of a single cell</strong></p><p>Nader Pourmand, Ph.D., University of California Santa Cruz, Santa Cruz, California</p><p>This solution proposes the use of a nano-sized pipette whose tiny tip can retrieve miniscule samples of a cell without perturbing its health, function, or gene expression. The pipette takes many repetitive cell samples over a period of minutes, hours, days, or weeks. These small samples can then be analyzed to monitor changes in gene expression that occur as a cell ages or undergoes other phenotypic changes.</p><p><strong>OTHER FINALISTS:</strong></p><p>Though not recipients of a monetary prize, the following meritorious solutions were selected to move on to Phase 2 of the competition.</p><ul><li><strong>Next generation automated cell tracking software to Follow That Cell and its progeny accurately in complex multicellular environments</strong></li></ul><p>Helen Blau, Ph.D. (team lead), Stanford University, Stanford, California</p><ul><li><strong>Development, optimization, and enhancement of fluorescent DNA-hairpin functionalized gold nanoparticles as imaging tools</strong></li></ul><p>Joseph Conrad, Ph.D. (team lead), Vanderbilt University, Nashville, Tennessee</p><ul><li><strong>Microfluidic droplet based platform for cell co-encapsulation and monitoring</strong></li></ul><p>Tania Konry, Ph.D., Northeastern University, Boston, Massachusetts</p><ul><li><strong>Synthetic nano-antibodies for real-time monitoring of cellular biomarkers</strong><br>Markita Landry, Ph.D., MIT, Cambridge, Massachusetts</li><li><strong>Single cell oncogenesis</strong></li></ul><p>Xin Lu, Ph.D., MD Anderson Cancer Center, Houston, Texas</p><ul><li><strong>Tracking the phenotype of single cells using multicolor flow cytometry combined with cell-specific barcodes.</strong></li></ul><p>Garry Nolan, Ph.D., Stanford University, Stanford, California</p><ul><li><strong>Flow of mechanical information in living cells</strong></li></ul><p>Frederick Sachs, Ph.D. (team lead), State University of New York at Buffalo, Buffalo, New York</p><ul><li><strong>RNA-seq</strong></li></ul><p>Hongjun Song, Ph.D. (team lead), Johns Hopkins University, Baltimore, Maryland</p><ul><li><strong>Dynamic tracking of cancer stem cells in native tumor microenvironments - single cell, dynamic monitoring of multi-gene expression in tumor tissues</strong></li></ul><p>Pak Kin Wong, Ph.D. (team lead), University of Arizona, Tucson, Arizona</p><ul><li><strong>Photostable multiplexing nanoassays for real-time molecular imaging of single live cells</strong></li></ul><p>X. Nancy Xu, Ph.D., Old Dominion University, Norfolk, Virginia</p><ul><li><strong>Development of micro-scale sampling probes for in situ mass spectrometry analysis of secretomes from live single cells</strong></li></ul><p>Zhibo Yang, Ph.D., University of Oklahoma, Norman, Oklahoma</p><article class="media media--type-image media--view-mode-default">
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