Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.

Structured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice,...

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Main Authors: Xing Zhou, Ming Lei, Dan Dan, Baoli Yao, Jia Qian, Shaohui Yan, Yanlong Yang, Junwei Min, Tong Peng, Tong Ye, Guangde Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4370656?pdf=render
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spelling doaj-9901ab8f8d4545a9a395e2dc569a199b2020-11-25T02:45:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012089210.1371/journal.pone.0120892Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.Xing ZhouMing LeiDan DanBaoli YaoJia QianShaohui YanYanlong YangJunwei MinTong PengTong YeGuangde ChenStructured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice, three raw images with a fixed phase-shift, normally 2π/3, are generally required. In this paper, we report a data processing algorithm based on the one-dimensional Hilbert transform, which needs only two raw images with arbitrary phase-shift for each single slice. The proposed algorithm is different from the previous two-dimensional Hilbert spiral transform algorithm in theory. The presented algorithm has the advantages of simpler data processing procedure, faster computation speed and better reconstructed image quality. The validity of the scheme is verified by imaging biological samples in our developed DMD-based LED-illumination SIM system.http://europepmc.org/articles/PMC4370656?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xing Zhou
Ming Lei
Dan Dan
Baoli Yao
Jia Qian
Shaohui Yan
Yanlong Yang
Junwei Min
Tong Peng
Tong Ye
Guangde Chen
spellingShingle Xing Zhou
Ming Lei
Dan Dan
Baoli Yao
Jia Qian
Shaohui Yan
Yanlong Yang
Junwei Min
Tong Peng
Tong Ye
Guangde Chen
Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
PLoS ONE
author_facet Xing Zhou
Ming Lei
Dan Dan
Baoli Yao
Jia Qian
Shaohui Yan
Yanlong Yang
Junwei Min
Tong Peng
Tong Ye
Guangde Chen
author_sort Xing Zhou
title Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
title_short Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
title_full Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
title_fullStr Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
title_full_unstemmed Double-exposure optical sectioning structured illumination microscopy based on Hilbert transform reconstruction.
title_sort double-exposure optical sectioning structured illumination microscopy based on hilbert transform reconstruction.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Structured illumination microscopy (SIM) with axially optical sectioning capability has found widespread applications in three-dimensional live cell imaging in recent years, since it combines high sensitivity, short image acquisition time, and high spatial resolution. To obtain one sectioned slice, three raw images with a fixed phase-shift, normally 2π/3, are generally required. In this paper, we report a data processing algorithm based on the one-dimensional Hilbert transform, which needs only two raw images with arbitrary phase-shift for each single slice. The proposed algorithm is different from the previous two-dimensional Hilbert spiral transform algorithm in theory. The presented algorithm has the advantages of simpler data processing procedure, faster computation speed and better reconstructed image quality. The validity of the scheme is verified by imaging biological samples in our developed DMD-based LED-illumination SIM system.
url http://europepmc.org/articles/PMC4370656?pdf=render
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AT junweimin doubleexposureopticalsectioningstructuredilluminationmicroscopybasedonhilberttransformreconstruction
AT tongpeng doubleexposureopticalsectioningstructuredilluminationmicroscopybasedonhilberttransformreconstruction
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AT guangdechen doubleexposureopticalsectioningstructuredilluminationmicroscopybasedonhilberttransformreconstruction
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