Cyclic Immunofluorescence (CycIF), A Highly Multiplexed Method for Single‐cell Imaging. Issue 4 (7th December 2016)

• Record Type: Journal Article
• Authors: Lin, Jia‐Ren; Fallahi‐Sichani, Mohammad; Chen, Jia‐Yun; Sorger, Peter K.
• Editors: Mahal, Lara; Romesberg, Floyd; Shah, Kavita; Shamu, Caroline; Strano, Michael S.; Thomas, Craig
• Is Part Of: Current protocols in chemical biology. Volume 8:Issue 4(2016)
• Page Start: 251
• Page End: 264
• Publication Date: 2016-12-07
• Subjects: CycIF -- immunofluorescence -- high‐content imaging -- multiplexing -- systems biology; Biochemistry -- Laboratory manuals; Chemical Phenomena; Biochemistry; Periodicals; Laboratory manuals; 572.078
• DOI: 10.1002/cpch.14
• Languages: English
• ISSNs: 2160-4762

Abstract

Abstract: Cyc lic I mmunof luorescence (CycIF) is a public‐domain method for performing highly multiplexed immunofluorescence imaging using a conventional epifluorescence microscope. It uses simple reagents and existing antibodies to construct images with up to 30 channels by sequential 4‐ to 6‐channel imaging followed by fluorophore inactivation. Three variant methods are described, the most generally useful of which involves staining fixed cells with antibodies directly conjugated to Alexa Fluor dyes and imaging in four colors, inactivating fluorophores using a mild base in the presence of hydrogen peroxide and light, and then performing another round of staining and imaging. Cell morphology is preserved through multiple rounds of CycIF, and signal‐to‐noise ratios appear to increase. Unlike antibody‐stripping methods, CycIF is gentle and optimized for monolayers of cultured cells. A second protocol involves indirect immunofluorescence and a third enables chemical inactivation of genetically encoded fluorescent proteins, allowing multiplex immunofluorescence to be combined with live‐cell analysis of cells expressing fluorescent reporter proteins. © 2016 by John Wiley & Sons, Inc.