This project provides state-of-the-art research technologies for NIAID's intramural infectious diseases, allergy, and immunology research programs. The new technologies are developed and validated and then applied in support of NIAID research. Technologies developed outside the NIH are likewise tested, evaluated, validated and, if appropriate, incorporated into the technology portfolio of the NIAID intramural program. The technologies supported include flow cytometry, confocal microscopy, DNA microarray, protein separation, mass spectrometry, peptide synthesis and protein sequencing. Many of these technologies are used in high containment laboratories critical to the Institute's infectious diseases and biodefense research agenda. In addition to technology development, the RTB provides advanced training in all aspects of the technologies in the Branchs portfolio. Flow Cytometry The mission of the Flow Cytometry Section is to provide the DIR with applicationspecific flow cytometric technologies, including instrumentation for high speed cell sorting and multi-color analysis, and to provide training, consultation, method development, and analysis for experiments involving flow cytometry. This mission is accomplished through the efforts of staff with extensive flow cytometry experience and with the use of eight cell sorters and eleven analyzers. Major goals are to provide access to state-of-the art technologies, to help design and run experiments, to facilitate data interpretation and to provide results that are of consistent high quality. Light Microscopy The mission of the Biological Imaging Section is to make available to DIR scientists advanced light microscopy imaging technologies and expertise in their use. This involves collaborating in both experimental design and instrument operation to best utilize the power of these cutting edge technologies, as well as to convey a basic understanding of the imaging process. These activities especially benefit those investigators whose specialty is not in microscopy or imaging. In practice, the Biological Imaging Section works collaboratively with laboratories within the DIR. Investigators are expected to participate in collection of their data, either as direct microscope operators or by selecting cells of interest, so that Biological Imaging Section staff can then collect the data. Often the collaboration begins much earlier, at the time of experimental design. The Biological Imaging Section advises on the most suitable instrument, appropriate labels, sample preparation, and best sampling regimens. Another responsibility of the Biological Imaging Section is to anticipate new directions in the imaging requirements of DIR and to insure that it is well-equipped and knowledgeable in those areas. Protein Chemistry The Protein Chemistry Section develops applications in the fields of peptide synthesis, N-terminal (Edman) sequencing, protein separation, assay development, and mass spectrometry. The RTB designs qualitative and quantitative physical-chemical and biochemical methods of detection and analysis that are customized to meet the specific research needs of DIR investigators. The Branch is also active in formulating and executing purification strategies for various types of molecules. This can also include customized small scale sample preparation and enrichment strategies for analysis by mass spectrometry. Another major activity of the RTB involves the development of more efficient and effective methods of sample preparation with a strong orientation towards mass spectroscopy to facilitate protein identification work. The Branch collaborates with DIR investigators to develop and validate protocols for protein separation and analysis for specific research programs of interest to the intramural research program. Microarray and Bioinformatics The mission of the Genomic Technologies Section is to enable DIR investigators to utilize microarray technology in their research programs. Application-specific microarrays and state of the art instrumentation and staff expertise are available to provide high performance for the whole microarray project life-cycle from experiment design through statistical analysis and interpretation. Investigators use the Genomic Technologies Section to investigate whole-genome expression profiles of many organisms including mouse, human, chimpanzee, Candida glabrata, Ixodes scapularis (tick), Mycobacterium tuberculosis, Strongyloides stercoralis (threadworm), Plasmodium falciparum (malaria), and Cryptococcus neoformans. Arrays that focus on micro RNA (miRNA) expression, genomic DNA, and experimental microarray applications are also available. The statistical and bioinformatics computing resources offered in the Genomic Technologies Section are also in high demand.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2009
Total Cost
$8,422,285
Indirect Cost
City
State
Country
Zip Code
Sekhar, Vandana; Pollicino, Teresa; Diaz, Giacomo et al. (2018) Infection with hepatitis C virus depends on TACSTD2, a regulator of claudin-1 and occludin highly downregulated in hepatocellular carcinoma. PLoS Pathog 14:e1006916
Kaur, Sukhbir; Elkahloun, Abdel G; Arakelyan, Anush et al. (2018) CD63, MHC class 1, and CD47 identify subsets of extracellular vesicles containing distinct populations of noncoding RNAs. Sci Rep 8:2577
Basu, Trisha; Seyedmousavi, Seyedmojtaba; Sugui, Janyce A et al. (2018) Aspergillus fumigatus alkaline protease 1 (Alp1/Asp f13) in the airways correlates with asthma severity. J Allergy Clin Immunol 141:423-425.e7
Ireland, Robin; Schwarz, Benjamin; Nardone, Glenn et al. (2018) Unique Francisella Phosphatidylethanolamine Acts as a Potent Anti-Inflammatory Lipid. J Innate Immun :1-15
Lee, Chang Hoon; Zhang, Hongwei H; Singh, Satya P et al. (2018) C/EBP? drives interactions between human MAIT cells and endothelial cells that are important for extravasation. Elife 7:
Matsuyama, Masashi; Martins, Andrew J; Shallom, Shamira et al. (2018) Transcriptional Response of Respiratory Epithelium to Nontuberculous Mycobacteria. Am J Respir Cell Mol Biol 58:241-252
Xie, Zhihui; Chen, Wei-Sheng; Yin, Yuzhi et al. (2018) Adrenomedullin surges are linked to acute episodes of the systemic capillary leak syndrome (Clarkson disease). J Leukoc Biol 103:749-759
Oakley, Miranda S; Verma, Nitin; Myers, Timothy G et al. (2018) Transcriptome analysis based detection of Plasmodium falciparum development in Anopheles stephensi mosquitoes. Sci Rep 8:11568
Sampaio, Elizabeth P; Ding, Li; Rose, Stacey R et al. (2018) Novel signal transducer and activator of transcription 1 mutation disrupts small ubiquitin-related modifier conjugation causing gain of function. J Allergy Clin Immunol 141:1844-1853.e2
Kauffman, K D; Sallin, M A; Sakai, S et al. (2018) Defective positioning in granulomas but not lung-homing limits CD4 T-cell interactions with Mycobacterium tuberculosis-infected macrophages in rhesus macaques. Mucosal Immunol 11:462-473

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