Lee, ChiaHung Wallace, Douglas Burke, Peter
We present super-resolution microscopy of isolated functional mitochondria, enabling real-time studies of structure and function (voltages) in response to pharmacological manipulation. Changes in mitochondrial membrane potential as a function of time and position can be imaged in different metabolic states (not possible in whole cells), created by ...
Zheng, Shuai Dadina, Neville Mozumdar, Deepto Lesiak, Lauren Martinez, Kayli Miller, Evan Schepartz, Alanna
The inner mitochondrial membrane (IMM) generates power to drive cell function, and its dynamics control mitochondrial health and cellular homeostasis. Here, we describe the cell-permeant, lipid-like small molecule MAO-N3 and use it to assemble high-density environmentally sensitive (HIDE) probes that selectively label and image the IMM in live cell...
Cox, Kristin E Turner, Michael A Amirfakhri, Siamak Lwin, Thinzar M Hosseini, Mojgan Ghosh, Pradipta Obonyo, Marygorret Murakami, Takashi Hoffman, Robert M Yazaki, Paul J
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IntroductionGastric cancer poses a major therapeutic challenge. Improved visualization of tumor margins at the time of gastrectomy with fluorescent tumor-specific antibodies could improve outcomes. The present report demonstrates the potential of targeting gastric cancer with a humanized anti-carcinoembryonic antigen (CEA) antibody in orthotopic mo...
Malakoutikhah, Morteza Mahran, Randa Gooran, Negin Masoumi, Ahmadreza Lundell, Katri Liljeblad, Arto Guiley, Keelan Dai, Shizhong Zheng, Qinheng Zhu, Lawrence
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Protein properties and interactions have been widely investigated by using external labels. However, the micromolar sensitivity of the current dyes limits their applicability due to the high material consumption and assay cost. In response to this challenge, we synthesized a series of cyanine5 (Cy5) dye-based quencher molecules to develop an extern...
Huang, Jianjun; 135208; Zheng, Dongbin; Fang, Yuyu; Dehaen, Wim; 6038;
Fluorescence microscopy has proven to be a crucial powerful tool to specifically visualize cellular organelles. In-depth visualization of the structure of mitochondria in living cells is of great value to better understand their function. Herein, based on our experience in construction of fluorescent difluoroboronate anchored acylhydrazones (BOAHY)...
Daus, Kevin Tharamak, Sorachat Pluempanupat, Wanchai Galie, Peter Theodoraki, Maria Theodorakis, Emmanuel Alpaugh, Mary
Accurate protein quantitation is essential for many cellular mechanistic studies. Existing technology relies on extrinsic sample evaluation that requires significant volumes of sample as well as addition of assay-specific reagents and importantly, is a terminal analysis. This study exploits the unique chemical features of a fluorescent molecular ro...
Tomimatsu, Kosuke Fujii, Takeru Bise, Ryoma Hosoda, Kazufumi Taniguchi, Yosuke Ochiai, Hiroshi Ohishi, Hiroaki Ando, Kanta Minami, Ryoma Tanaka, Kaori
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Funder: - Medical Research Center Initiative for High Depth Omics. / Funder: - MEXT | JST | Fusion Oriented REsearch for disruptive Science and Technology (FOREST), JPMJFR2251. / Cell states are regulated by the response of signaling pathways to receptor ligand-binding and intercellular interactions. High-resolution imaging has been attempted to ex...
Mehta, Sohum Zhang, Jin Lyons, Anne
As cell signaling research has advanced, it has become clearer that signal transduction has complex spatiotemporal regulation that goes beyond foundational linear transduction models. Several technologies have enabled these discoveries, including fluorescent biosensors designed to report live biochemical signaling events. As genetically encoded and...
Neves Sao Pedro, M. (author)
Continuous biomanufacturing is considered the future phase for the optimization of production processes in the biopharmaceutical industry. Productivity, product quality and consistency are greatly improved while production costs and environmental footprint are drastically reduced. The manufacturing of monoclonal antibodies (mAbs), an important biop...
Dynes, Joseph Yeromin, Andriy Cahalan, Michael
We used electrophysiology and Ca2+ channel tethering to evaluate the performance of jGCaMP8 genetically encoded Ca2+ indicators (GECIs). Orai1 Ca2+ channel-jGCaMP8 fusions were transfected into HEK 293A cells and jGCaMP8 fluorescence responses recorded by simultaneous total internal reflection fluorescence microscopy and whole-cell patch clamp elec...