Emmanouil D. Karagiannis

ORCID: 0000-0003-0131-6552
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About
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Research Areas
  • RNA Interference and Gene Delivery
  • Protease and Inhibitor Mechanisms
  • Advanced biosensing and bioanalysis techniques
  • Angiogenesis and VEGF in Cancer
  • Single-cell and spatial transcriptomics
  • Nanoparticle-Based Drug Delivery
  • Cancer Genomics and Diagnostics
  • Cell Adhesion Molecules Research
  • Lipid Membrane Structure and Behavior
  • Force Microscopy Techniques and Applications
  • Advanced Electron Microscopy Techniques and Applications
  • Corneal Surgery and Treatments
  • Chemokine receptors and signaling
  • CRISPR and Genetic Engineering
  • Cancer, Hypoxia, and Metabolism
  • Retinal Diseases and Treatments
  • Blood Coagulation and Thrombosis Mechanisms
  • RNA and protein synthesis mechanisms
  • Proteoglycans and glycosaminoglycans research
  • Evolution and Genetic Dynamics
  • Immunotherapy and Immune Responses
  • Pluripotent Stem Cells Research
  • Advanced Fluorescence Microscopy Techniques
  • Peptidase Inhibition and Analysis
  • Cell Image Analysis Techniques

Massachusetts Institute of Technology
2012-2025

McGovern Institute for Brain Research
2015-2025

Metropolitan Hospital
2022

IIT@MIT
2021

Engineering Arts (United States)
2021

Allen Institute
2021

Howard Hughes Medical Institute
2021

Johns Hopkins Medicine
2004-2010

Johns Hopkins University
2004-2010

University of Maryland, Baltimore
2005

Identifying transcript location in cells where specific RNAs occur within a cell or tissue has been limited by technology and imaging capabilities. Expansion microscopy allowed for better visualization of small structures expanding the tissues with polymer- hydrogel-based system. Alon et al. combined expansion long-read situ RNA sequencing, resulting more precise transcripts. This method, termed “ExSeq” was used to detect RNAs, both new transcripts those previously demonstrated localize...

10.1126/science.aax2656 article EN Science 2021-01-28

10.1038/s43018-020-0026-6 article EN Nature Cancer 2020-02-17
Emma Laks Andrew McPherson Hans Zahn Daniel Lai Adi Steif and 95 more Jazmine Brimhall Justina Biele Beixi Wang Tehmina Masud Jerome Ting Diljot Grewal Cydney Nielsen Samantha Leung Viktoria Bojilova Maia A. Smith Oleg Golovko Steven S.S. Poon Peter Eirew Farhia Kabeer Teresa Ruiz de Algara So Ra Lee M. Jafar Taghiyar Curtis Huebner Jessica Ngo Tim Hon Man Chan Spencer Vatrt-Watts Pascale Walters Nafis Abrar Sophia Chan Matt Wiens Lauren Martin R. Wilder Scott T. Michael Underhill Elizabeth A. Chavez Christian Steidl Daniel Da Costa Yussanne Ma Robin Coope Richard Corbett Stephen Pleasance Richard A. Moore Andrew J. Mungall Colin Mar Fergus Cafferty Karen A. Gelmon Stephen Chia Marco A. Marra Carl L. Hansen Sohrab P. Shah Samuel Aparício Gregory J. Hannon Giorgia Battistoni Dario Bressan Ian G. Cannell Hannah Casbolt Cristina Jauset Tatjana Kovačević Claire M. Mulvey Fiona Nugent Marta Ribes Isabella Pearsall Fatime Qosaj Kirsty Sawicka Sophia A. Wild Elena Williams Samuel Aparício Emma Laks Yangguang Li Ciara H. O’Flanagan Austin Smith Teresa Ruíz Shankar Balasubramanian Maximillian Lee Bernd Bodenmiller Marcel Burger Laura Kuett Sandra Tietscher Jonas Windager Edward S. Boyden Shahar Alon Yi Cui Amauche Emenari Dan Goodwin Emmanouil D. Karagiannis Anubhav Sinha Asmamaw T. Wassie Carlos Caldas Alejandra Bruna Maurizio Callari Wendy Greenwood Giulia Lerda Yaniv Lubling Alastair Marti Oscar M. Rueda Abigail Shea Owen Harris Robby Becker Flaminia Grimaldi Suvi Harris Sara Lisa Vogl

Accurate measurement of clonal genotypes, mutational processes, and replication states from individual tumor-cell genomes will facilitate improved understanding tumor evolution. We have developed DLP+, a scalable single-cell whole-genome sequencing platform implemented using commodity instruments, image-based object recognition, open source computational methods. Using we generated resource 51,926 matched cell images diverse types including lines, xenografts, diagnostic samples with limited...

10.1016/j.cell.2019.10.026 article EN cc-by-nc-nd Cell 2019-11-01

Abstract A holistic understanding of tissue and organ structure function requires the detection molecular constituents in their original three-dimensional (3D) context. Imaging mass cytometry (IMC) enables simultaneous up to 40 antigens transcripts using metal-tagged antibodies but has so far been restricted two-dimensional imaging. Here we report development 3D IMC for multiplexed analysis at single-cell resolution demonstrate utility technology by human breast cancer samples. The resulting...

10.1038/s43018-021-00301-w article EN cc-by Nature Cancer 2021-12-24
Sohrab Salehi Farhia Kabeer Nicholas Ceglia Mirela Andronescu Marc Williams and 95 more Kieran R. Campbell Tehmina Masud Beixi Wang Justina Biele Jazmine Brimhall David Gee Hakwoo Lee Jerome Ting Allen W. Zhang Hoa Tran Ciara H. O’Flanagan Fatemeh Dorri Nicole Rusk Teresa Ruiz de Algara So Ra Lee Brian Yu Chieh Cheng Peter Eirew Takako Kono Jenifer Pham Diljot Grewal Daniel Lai Richard A. Moore Andrew J. Mungall Marco A. Marra Gregory J. Hannon Giorgia Battistoni Dario Bressan Ian G. Cannell Hannah Casbolt Atefeh Fatemi Cristina Jauset Tatjana Kovačević Claire M. Mulvey Fiona Nugent Marta Ribes Isabella Pearsall Fatime Qosaj Kirsty Sawicka Sophia A. Wild Elena Williams Emma Laks Yangguang Li Ciara H. O’Flanagan Austin Smith Teresa Ruíz Daniel Lai Andrew Roth Shankar Balasubramanian Maximillian Lee Bernd Bodenmiller Marcel Burger Laura Kuett Sandra Tietscher Jonas Windhager Edward S. Boyden Shahar Alon Yi Cui Amauche Emenari Dan Goodwin Emmanouil D. Karagiannis Anubhav Sinha Asmamaw T. Wassie Carlos Caldas Alejandra Bruna Maurizio Callari Wendy Greenwood Giulia Lerda Yaniv Eyal-Lubling Oscar M. Rueda Abigail Shea Owen Harris Robby Becker Flaminia Grimaldi Suvi Harris Sara Lisa Vogl Joanna Weselak Johanna A. Joyce Spencer S. Watson Ignacio Vázquez-Garćıa Simon Tavaré Khanh N. Dinh Eyal Fisher Russell Kunes N. A. Walton Mohammad Al Sa’d Nick Chornay A. Dariush E. A. González-Solares Carlos González‐Fernández A. Yoldaş Neil S. Millar Tristan Whitmarsh Xiaowei Zhuang Jean Fan Hsuan Lee

10.1038/s41586-021-03648-3 article EN Nature 2021-06-23
Tyler Funnell Ciara H. O’Flanagan Marc Williams Andrew McPherson Steven McKinney and 95 more Farhia Kabeer Hakwoo Lee Sohrab Salehi Ignacio Vázquez-Garćıa Hongyu Shi Emily L Leventhal Tehmina Masud Peter Eirew Damian Yap Allen W. Zhang Jamie Lim Beixi Wang Jazmine Brimhall Justina Biele Jerome Ting Vinci Au Michael Van Vliet Yifei Liu Sean Beatty Daniel Lai Jenifer Pham Diljot Grewal Douglas N. Abrams Eliyahu Havasov Samantha Leung Viktoria Bojilova Richard A. Moore Nicole Rusk Florian Uhlitz Nicholas Ceglia Adam C. Weiner Elena Zaikova J. Maxwell Douglas Dmitriy Zamarin Britta Weigelt Sarah H. Kim Arnaud Da Cruz Paula Jorge S. Reis‐Filho Spencer D. Martin Yangguang Li Hongxia Xu Teresa Ruiz de Algara So Ra Lee Viviana Cerda Llanos David G. Huntsman Jessica N. McAlpine Gregory J. Hannon Georgia Battistoni Dario Bressan Ian G. Cannell Hannah Casbolt Cristina Jauset Tatjana Kovačević Claire M. Mulvey Fiona Nugent Marta Ribes Isabella Pearson Fatime Qosaj Kirsty Sawicka Sophia A. Wild Elena Williams Emma Laks Austin Smith Daniel Lai Andrew Roth Shankar Balasubramanian Maximilian Lee Bernd Bodenmiller Marcel Burger Laura Kuett Sandra Tietscher Jonas Windhager Edward S. Boyden Shahar Alon Yi Cui Amauche Emenari Daniel Goodwin Emmanouil D. Karagiannis Anubhav Sinha Asmamaw T. Wassie Carlos Caldas Alejandra Bruna Maurizio Callari Wendy Greenwood Giulia Lerda Yaniv Eyal-Lubling Oscar M. Rueda Abigail Shea Owen Harris Robby Becker Flaminia Grimaldo Suvi Harris Sara Lisa Vogl Johanna A. Joyce Spencer S. Watson

How cell-to-cell copy number alterations that underpin genomic instability

10.1038/s41586-022-05249-0 article EN cc-by Nature 2022-10-26

Abstract Lipid membranes are key to the nanoscale compartmentalization of biological systems, but fluorescent visualization them in intact tissues, with precision, is challenging do high labeling density. Here, we report ultrastructural membrane expansion microscopy (umExM), which combines an innovative label and optimized protocol, support dense tissues for visualization. We validate signal-to-background ratio, uniformity continuity, umExM brain slices, supports imaging proteins at a...

10.1038/s41467-025-56641-z article EN cc-by Nature Communications 2025-02-12

Abstract Lipids are fundamental building blocks of cells and their organelles, yet nanoscale resolution imaging lipids has been largely limited to electron microscopy techniques. We introduce validate a chemical tag that enables lipid membranes be imaged optically at via lipid-optimized form expansion microscopy, which we call membrane (mExM). mExM, novel post-expansion antibody labeling protocol, protein-lipid relationships in organelles such as mitochondria, the endoplasmic reticulum,...

10.1101/829903 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-11-04
Dimitra Georgopoulou Maurizio Callari Oscar M. Rueda Abigail Shea Alistair Martin and 95 more Agnese Giovannetti Fatime Qosaj A. Dariush Suet‐Feung Chin Larissa S. Carnevalli Elena Provenzano Wendy Greenwood Giulia Lerda Elham Esmaeilishirazifard Martin O’Reilly Violeta Serra Dario Bressan H. Raza Ali M. Al Sa’d Shahar Alon Samuel Aparício Giorgia Battistoni Shankar Balasubramanian Robert O. Becker Bernd Bodenmiller E. S. Boyden Dario Bressan Alejandra Bruna Marcel Burger Carlos Caldas Maurizio Callari Ian G. Cannell Helen Casbolt N. Chornay Yi Cui A. Dariush K. Dinh A. Emenari Y. Eyal-Lubling Jean Fan Ali Fatemi Edward A. Fisher E. A. González-Solares C. Gónzalez-Fernández Douglas C. Goodwin Wendy Greenwood Francesco Grimaldi Gregory J. Hannon Owen Harris Shelley Harris Cristina Jauset Johanna A. Joyce Emmanouil D. Karagiannis Tatjana Kovačević Laura Kuett Russell Kunes Yoldaş A. Küpcü Daniel Lai Emma Laks Hsuan Lee M. Lee Giulia Lerda Y. Li Andrew McPherson Neal L. Millar Claire M. Mulvey Fiona Nugent Ciara H. O’Flanagan Marta Pàez‐Ribes I. Pearsall Fatime Qosaj Andrew Roth Oscar M. Rueda Tamara Ruiz Kirsty Sawicka Leonardo A. Sepúlveda Sohrab P. Shah Abigail Shea Anubhav Sinha Adrian L. Smith S. Tavaré Sandra Tietscher Ignacio Vázquez-Garćıa Siegfried Vogl N. A. Walton Asmamaw T. Wassie Spencer S. Watson Joanna Weselak Sonja Wild Elena Williams Jonas Windhager Tristan Whitmarsh C. Xia Ping Zheng Xiaowei Zhuang Gordon B. Mills H. Raza Ali Sabina S. Cosulich Gregory J. Hannon Alejandra Bruna

The heterogeneity of breast cancer plays a major role in drug response and resistance has been extensively characterized at the genomic level. Here, single-cell mass cytometry (BCMC) panel is optimized to identify cell phenotypes their oncogenic signalling states biobank patient-derived tumour xenograft (PDTX) models representing diversity human cancer. BCMC identifies 13 cellular (11 2 murine), associated with both subtypes specific features. Pre-treatment phenotypic composition determinant...

10.1038/s41467-021-22303-z article EN cc-by Nature Communications 2021-03-31

Matrix metalloproteinases (MMPs) are a class of extracellular and membrane-bound proteases involved in an array physiological processes, including angiogenesis. We present detailed computational model MMP9 activation inhibition. Our is validated to existing biochemical experimental data. determine kinetic rate constants for the processes by MMP3, MMP10, MMP13, trypsin; inhibition tissue inhibitors (TIMPs) 1 2; deactivation. This approach allows us investigate discrepancies our understanding...

10.1074/jbc.m611500200 article EN cc-by Journal of Biological Chemistry 2007-09-12

Abstract Lipid membranes are key to the nanoscale compartmentalization of biological systems, but fluorescent visualization them in intact tissues, with precision, is challenging do high labeling density. Here, we report ultrastructural membrane expansion microscopy (umExM), which combines a novel label and optimized protocol, support dense tissues for visualization. We validated signal-to-background ratio, uniformity continuity, umExM brain slices, supported imaging proteins at resolution...

10.1101/2024.03.07.583776 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-03-08

One well documented family of enzymes responsible for the proteolytic processes that occur in extracellular matrix is soluble and membrane-associated metalloproteinases. Here we present first theoretical model biochemical network describing proteolysis collagen I by metalloproteinases 2 (MMP2) membrane type 1 (MT1-MMP) presence tissue inhibitor (TIMP2) a bulk, cell-free, stirred environment. The can serve as tool quantitatively activation MMP2 proenzyme (pro-MMP2), ectodomain shedding...

10.1074/jbc.m403627200 article EN cc-by Journal of Biological Chemistry 2004-07-13

We introduce a systematic computational methodology based on bioinformatics that has enabled us to identify and classify >120 endogenous peptide inhibitors of endothelial cell proliferation migration. These peptides are derived from members the type IV collagen, thrombospondin, CXC chemokine protein families, as well somatotropin hormones, serpins, various kringle-containing proteins. Their activity in suppressing migration cells vitro provides proof principle for validity this method....

10.1073/pnas.0803241105 article EN Proceedings of the National Academy of Sciences 2008-09-10

Angiogenesis or neovascularization, the process of new blood vessel formation from preexisting microvasculature, involves interactions among several cell types including parenchymal, endothelial cells, and immune cells. The vessels is tightly regulated by a balance between endogenous proangiogenic antiangiogenic factors to maintain homeostasis in tissue; tumor progression metastasis breast cancer have been shown be angiogenesis-dependent. We previously introduced systematic methodology...

10.1593/neo.09620 article EN cc-by-nc-nd Neoplasia 2009-12-01

Cell penetrating peptides have demonstrated potential to facilitate the cellular delivery of therapeutic molecules. Here we develop a set 50 cell peptide based formulations with deliver small interfering RNAs intercellularly. The transfection efficacy siRNA containing lipid-like nanoparticles decorated different was evaluated both in vitro and vivo correlated physical chemical properties. In vitro, these particles were internalized primarily through macropinocytosis. When presented bone...

10.1021/nn4027382 article EN ACS Nano 2013-09-18

Angiogenesis is the formation of neovasculature from a pre-existing vascular network. Progression solid tumors including lung cancer angiogenesis-dependent. We previously introduced bioinformatics-based methodology to identify endogenous anti-angiogenic peptide sequences, and validated these predictions in vitro human umbilical vein endothelial cell (HUVEC) proliferation migration assays.One family peptides with high activity derived alpha-fibrils type IV collagen. Based on results...

10.1186/1471-2407-10-29 article EN cc-by BMC Cancer 2010-02-01
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