Literature DB >> 34059826

A pairwise distance distribution correction (DDC) algorithm to eliminate blinking-caused artifacts in SMLM.

Christopher H Bohrer1,2, Xinxing Yang1, Shreyasi Thakur3, Xiaoli Weng1, Brian Tenner4, Ryan McQuillen1, Brian Ross4, Matthew Wooten5, Xin Chen5, Jin Zhang4, Elijah Roberts2, Melike Lakadamyali3, Jie Xiao6.   

Abstract

Single-molecule localization microscopy (SMLM) relies on the blinking behavior of a fluorophore, which is the stochastic switching between fluorescent and dark states. Blinking creates multiple localizations belonging to the same fluorophore, confounding quantitative analyses and interpretations. Here we present a method, termed distance distribution correction (DDC), to eliminate blinking-caused repeat localizations without any additional calibrations. The approach relies on obtaining the true pairwise distance distribution of different fluorophores naturally from the imaging sequence by using distances between localizations separated by a time much longer than the average fluorescence survival time. We show that, using the true pairwise distribution, we can define and maximize the likelihood, obtaining a set of localizations void of blinking artifacts. DDC results in drastic improvements in obtaining the closest estimate of the true spatial organization and number of fluorescent emitters in a wide range of applications, enabling accurate reconstruction and quantification of SMLM images.

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Year:  2021        PMID: 34059826      PMCID: PMC9040192          DOI: 10.1038/s41592-021-01154-y

Source DB:  PubMed          Journal:  Nat Methods        ISSN: 1548-7091            Impact factor:   47.990


  71 in total

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4.  NIH Image to ImageJ: 25 years of image analysis.

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5.  Chromosome organization by a nucleoid-associated protein in live bacteria.

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6.  Influence of FtsZ GTPase activity and concentration on nanoscale Z-ring structure in vivo revealed by three-dimensional Superresolution imaging.

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7.  Transcription-factor-mediated DNA looping probed by high-resolution, single-molecule imaging in live E. coli cells.

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9.  Optimizing Imaging Conditions for Demanding Multi-Color Super Resolution Localization Microscopy.

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Journal:  Nat Methods       Date:  2019-09-27       Impact factor: 28.547

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  8 in total

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7.  A density-based enrichment measure for assessing colocalization in single-molecule localization microscopy data.

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  8 in total

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