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A Protocol for the Acquisition of Comprehensive Proteomics Data from Single Cases Using Formalin-Fixed Paraffin Embedded Sections.
Acland, Mitchell; Mittal, Parul; Arentz, Georgia; Whitehead, Fergus; Hoffmann, Peter; Klingler-Hoffmann, Manuela; Oehler, Martin K.
Afiliação
  • Acland M; Adelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, Australia.
  • Mittal P; Clinical & Health Science, Mawson Lakes Campus, University of South Australia, Adelaide, SA 5095, Australia.
  • Arentz G; Adelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, Australia.
  • Whitehead F; Clinpath Pathology, 21 James Congdon Drive, Mile End, Adelaide, SA 5031, Australia.
  • Hoffmann P; Clinical & Health Science, Mawson Lakes Campus, University of South Australia, Adelaide, SA 5095, Australia.
  • Klingler-Hoffmann M; Clinical & Health Science, Mawson Lakes Campus, University of South Australia, Adelaide, SA 5095, Australia.
  • Oehler MK; Department of Gynaecological Oncology, Royal Adelaide Hospital, North Terrace, Adelaide, SA 5000, Australia.
Methods Protoc ; 5(4)2022 Jul 10.
Article em En | MEDLINE | ID: mdl-35893583
The molecular analysis of small or rare patient tissue samples is challenging and often limited by available technologies and resources, such as reliable antibodies against a protein of interest. Although targeted approaches provide some insight, here, we describe the workflow of two complementary mass spectrometry approaches, which provide a more comprehensive and non-biased analysis of the molecular features of the tissue of interest. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) generates spatial intensity maps of molecular features, which can be easily correlated with histology. Additionally, liquid chromatography tandem mass spectrometry (LC-MS/MS) can identify and quantify proteins of interest from a consecutive section of the same tissue. Here, we present data from concurrent precancerous lesions from the endometrium and fallopian tube of a single patient. Using this complementary approach, we monitored the abundance of hundreds of proteins within the precancerous and neighboring healthy regions. The method described here represents a useful tool to maximize the number of molecular data acquired from small sample sizes or even from a single case. Our initial data are indicative of a migratory phenotype in these lesions and warrant further research into their malignant capabilities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article