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MIBI-TOF: A multiplexed imaging platform relates cellular phenotypes and tissue structure.
Keren, Leeat; Bosse, Marc; Thompson, Steve; Risom, Tyler; Vijayaragavan, Kausalia; McCaffrey, Erin; Marquez, Diana; Angoshtari, Roshan; Greenwald, Noah F; Fienberg, Harris; Wang, Jennifer; Kambham, Neeraja; Kirkwood, David; Nolan, Garry; Montine, Thomas J; Galli, Stephen J; West, Robert; Bendall, Sean C; Angelo, Michael.
Afiliação
  • Keren L; Department of Pathology, Stanford University, Stanford, CA.
  • Bosse M; Department of Pathology, Stanford University, Stanford, CA.
  • Thompson S; Department of Pathology, Stanford University, Stanford, CA.
  • Risom T; Department of Pathology, Stanford University, Stanford, CA.
  • Vijayaragavan K; Department of Pathology, Stanford University, Stanford, CA.
  • McCaffrey E; Department of Pathology, Stanford University, Stanford, CA.
  • Marquez D; Immunology Program, Stanford University School of Medicine, Stanford, CA.
  • Angoshtari R; Department of Pathology, Stanford University, Stanford, CA.
  • Greenwald NF; Department of Pathology, Stanford University, Stanford, CA.
  • Fienberg H; Department of Pathology, Stanford University, Stanford, CA.
  • Wang J; Cancer Biology Program, Stanford University School of Medicine, Stanford, CA.
  • Kambham N; Department of Pathology, Stanford University, Stanford, CA.
  • Kirkwood D; Department of Pathology, Stanford University, Stanford, CA.
  • Nolan G; Department of Pathology, Stanford University, Stanford, CA.
  • Montine TJ; Department of Pathology, Stanford University, Stanford, CA.
  • Galli SJ; Department of Microbiology and Immunology, Stanford University, Stanford, CA.
  • West R; Department of Pathology, Stanford University, Stanford, CA.
  • Bendall SC; Department of Pathology, Stanford University, Stanford, CA.
  • Angelo M; Department of Pathology, Stanford University, Stanford, CA.
Sci Adv ; 5(10): eaax5851, 2019 10.
Article em En | MEDLINE | ID: mdl-31633026
ABSTRACT
Understanding tissue structure and function requires tools that quantify the expression of multiple proteins while preserving spatial information. Here, we describe MIBI-TOF (multiplexed ion beam imaging by time of flight), an instrument that uses bright ion sources and orthogonal time-of-flight mass spectrometry to image metal-tagged antibodies at subcellular resolution in clinical tissue sections. We demonstrate quantitative, full periodic table coverage across a five-log dynamic range, imaging 36 labeled antibodies simultaneously with histochemical stains and endogenous elements. We image fields of view up to 800 µm × 800 µm at resolutions down to 260 nm with sensitivities approaching single-molecule detection. We leverage these properties to interrogate intrapatient heterogeneity in tumor organization in triple-negative breast cancer, revealing regional variability in tumor cell phenotypes in contrast to a structured immune response. Given its versatility and sample back-compatibility, MIBI-TOF is positioned to leverage existing annotated, archival tissue cohorts to explore emerging questions in cancer, immunology, and neurobiology.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espectrometria de Massa de Íon Secundário Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espectrometria de Massa de Íon Secundário Idioma: En Ano de publicação: 2019 Tipo de documento: Article