| Literature DB >> 23938572 |
Meredith H Brenner1, Dawen Cai, Joel A Swanson, Jennifer P Ogilvie.
Abstract
Imaging multiple fluorescent proteins (FPs) by two-photon microscopy has numerous applications for studying biological processes in thick and live samples. Here we demonstrate a setup utilizing a single broadband laser and a phase-only pulse-shaper to achieve imaging of three FPs (mAmetrine, TagRFPt, and mKate2) in live mammalian cells. Phase-shaping to achieve selective excitation of the FPs in combination with post-imaging linear unmixing enables clean separation of the fluorescence signal of each FP. This setup also benefits from low overall cost and simple optical alignment, enabling easy adaptation in a regular biomedical research laboratory.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23938572 PMCID: PMC3724397 DOI: 10.1364/OE.21.017256
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894