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Multielectrode Spectroscopy Enables Rapid and Sensitive Molecular Profiling of Extracellular Vesicles.
Kilic, Tugba; Cho, Young Kwan; Jeong, Naebong; Shin, Ik-Soo; Carter, Bob S; Balaj, Leonora; Weissleder, Ralph; Lee, Hakho.
Afiliação
  • Kilic T; Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, United States.
  • Cho YK; Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Jeong N; Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, United States.
  • Shin IS; Department of Chemistry, Kennedy College of Sciences, University of Massachusetts Lowell, Lowell, Massachusetts 01854, United States.
  • Carter BS; Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, United States.
  • Balaj L; Department of Chemistry, Soongsil University, Seoul 06978, South Korea.
  • Weissleder R; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Lee H; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
ACS Cent Sci ; 8(1): 110-117, 2022 Jan 26.
Article em En | MEDLINE | ID: mdl-35111901
ABSTRACT
Detecting protein markers in extracellular vesicles (EVs) is becoming a useful tool for basic research and clinical diagnoses. Most EV protein assays, however, require lengthy processes-conjugating affinity ligands onto sensing substrates and affixing EVs with additional labels to maximize signal generation. Here, we present an iPEX (impedance profiling of extracellular vesicles) system, an all-electrical strategy toward fast, multiplexed EV profiling. iPEX adopts one-step electropolymerization to rapidly functionalize sensor electrodes with antibodies; it then detects EV proteins in a label-free manner through impedance spectroscopy. The approach streamlines the entire EV assay, from sensor preparation to signal measurements. We achieved (i) fast immobilization of antibodies (<3 min) per electrode; (ii) high sensitivity (500 EVs/mL) without secondary labeling; and (iii) parallel detection (quadruple) in a single chip. A potential clinical utility was demonstrated by directly analyzing plasma samples from glioblastoma multiforme patients.

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

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