α-Cyano-4-hydroxycinnamic Acid and Tri-Potassium Citrate Salt Pre-Coated Silicon Nanopost Array Provides Enhanced Lipid Detection for High Spatial Resolution MALDI Imaging Mass Spectrometry.


Journal

Analytical chemistry
ISSN: 1520-6882
Titre abrégé: Anal Chem
Pays: United States
ID NLM: 0370536

Informations de publication

Date de publication:
14 09 2021
Historique:
pubmed: 28 8 2021
medline: 18 9 2021
entrez: 27 8 2021
Statut: ppublish

Résumé

We have developed a pre-coated substrate for matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) that enables high spatial resolution mapping of both phospholipids and neutral lipid classes in positive ion mode as metal cation adducts. The MALDI substrates are constructed by depositing a layer of α-cyano-4-hydroxycinnamic acid (CHCA) and potassium salts onto silicon nanopost arrays (NAPA) prior to tissue mounting. The matrix/salt pre-coated NAPA substrate significantly enhances all detected lipid signals allowing lipids to be detected at lower laser energies than bare NAPA. The improved sensitivity at lower laser energy enabled ion images to be generated at 10 μm spatial resolution from rat retinal tissue. Optimization of matrix pre-coated NAPA consisted of testing lithium, sodium, and potassium salts along with various matrices to investigate the increased sensitivity toward lipids for MALDI IMS experiments. It was determined that pre-coating NAPA with CHCA and potassium salts before thaw-mounting of tissue resulted in a signal intensity increase of at least 5.8 ± 0.1-fold for phospholipids and 2.0 ± 0.1-fold for neutral lipids compared to bare NAPA. Pre-coating NAPA with matrix and salt also reduced the necessary laser power to achieve desorption/ionization by ∼35%. This reduced the effective diameter of the ablation area from 13 ± 2 μm down to 8 ± 1 μm, enabling high spatial resolution MALDI IMS. Using pre-coated NAPA with CHCA and potassium salts offers a MALDI IMS substrate with broad molecular coverage of lipids in a single polarity that eliminates the need for extensive sample preparation after sectioning.

Identifiants

pubmed: 34449196
doi: 10.1021/acs.analchem.1c01560
doi:

Substances chimiques

Coumaric Acids 0
Phospholipids 0
alpha-cyano-4-hydroxycinnamate 28166-41-8
Citric Acid 2968PHW8QP
Potassium Citrate EE90ONI6FF
Potassium RWP5GA015D
Silicon Z4152N8IUI

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

12243-12249

Subventions

Organisme : NIGMS NIH HHS
ID : P41 GM103391
Pays : United States
Organisme : NEI NIH HHS
ID : U54 EY032442
Pays : United States

Auteurs

Martin Dufresne (M)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.

Jarod A Fincher (JA)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.

Nathan Heath Patterson (NH)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.

Kevin L Schey (KL)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States.

Jeremy L Norris (JL)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States.

Richard M Caprioli (RM)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232, United States.

Jeffrey M Spraggins (JM)

Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37205, United States.
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Cell & Developmental Biology, Vanderbilt University, Nashville, Tennessee 37232, United States.

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Classifications MeSH