Tracking intracellular uptake and localisation of alkyne tagged fatty acids using Raman spectroscopy

被引:28
|
作者
Jamieson, Lauren E. [1 ]
Greaves, Jennifer [2 ]
McLellan, Jayde A. [3 ]
Munro, Kevin R. [3 ]
Tomkinson, Nicholas C. O. [3 ]
Chamberlain, Luke H. [2 ]
Faulds, Karen [1 ]
Graham, Duncan [1 ]
机构
[1] Univ Strathclyde, Ctr Mol Nanometrol, Dept Pure & Appl Chem, WestCHEM,Technol & Innovat Ctr, 99 George St, Glasgow G1 1RD, Lanark, Scotland
[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, 161 Cathedral St, Glasgow G4 0RE, Lanark, Scotland
[3] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, 295 Cathedral St, Glasgow G1 1XL, Lanark, Scotland
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Spectroscopy; Raman; Lipids; Fatty acids; Alkyne tag; Intracellular imaging; LIVE CELLS; MICROSCOPY; MACROPHAGES; SCATTERING; LIPIDS; VISUALIZATION; BIOMOLECULES; METABOLISM; PROTEINS; TISSUES;
D O I
10.1016/j.saa.2018.01.064
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Intracellular uptake, distribution and metabolism of lipids are tightly regulated characteristics in healthy cells. An analytical technique capable of understanding these characteristics with a high level of species specificity in a minimally invasive manner is highly desirable in order to understand better how these become disrupted during disease. In this study, the uptake and distribution of three different alkyne tagged fatty acids in single cells were monitored and compared, highlighting the ability of Raman spectroscopy combined with alkyne tags for better understanding of the fine details with regard to uptake, distribution and metabolism of very chemically specific lipid species. This indicates the promise of using Raman spectroscopy directly with alkyne tagged lipids for cellular studies as opposed to subsequently clicking of a fluorophore onto the alkyne for fluorescence imaging. (C) 2018 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license.
引用
收藏
页码:30 / 36
页数:7
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