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Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers

[Image: see text] We use a double nanohole optical tweezer to analyze the protein composition of egg white through analysis of many individual protein trapping events. The proteins are grouped by mass based on two metrics: standard deviation of the trapping laser intensity fluctuations from the prot...

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Autores principales: Hacohen, Noa, Ip, Candice J. X., Gordon, Reuven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641915/
https://www.ncbi.nlm.nih.gov/pubmed/31458737
http://dx.doi.org/10.1021/acsomega.8b00651
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author Hacohen, Noa
Ip, Candice J. X.
Gordon, Reuven
author_facet Hacohen, Noa
Ip, Candice J. X.
Gordon, Reuven
author_sort Hacohen, Noa
collection PubMed
description [Image: see text] We use a double nanohole optical tweezer to analyze the protein composition of egg white through analysis of many individual protein trapping events. The proteins are grouped by mass based on two metrics: standard deviation of the trapping laser intensity fluctuations from the protein diffusion and the time constant of these fluctuations coming from the autocorrelation. Quantitative analysis is demonstrated for artificial samples, and then, the approach is applied to real egg white. The composition found from real egg white corresponds well to past reports using gel electrophoresis. This approach differs from past works by allowing for individual protein analysis in heterogeneous solutions without the need for denaturing, labeling, or tethering.
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spelling pubmed-66419152019-08-27 Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers Hacohen, Noa Ip, Candice J. X. Gordon, Reuven ACS Omega [Image: see text] We use a double nanohole optical tweezer to analyze the protein composition of egg white through analysis of many individual protein trapping events. The proteins are grouped by mass based on two metrics: standard deviation of the trapping laser intensity fluctuations from the protein diffusion and the time constant of these fluctuations coming from the autocorrelation. Quantitative analysis is demonstrated for artificial samples, and then, the approach is applied to real egg white. The composition found from real egg white corresponds well to past reports using gel electrophoresis. This approach differs from past works by allowing for individual protein analysis in heterogeneous solutions without the need for denaturing, labeling, or tethering. American Chemical Society 2018-05-16 /pmc/articles/PMC6641915/ /pubmed/31458737 http://dx.doi.org/10.1021/acsomega.8b00651 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Hacohen, Noa
Ip, Candice J. X.
Gordon, Reuven
Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title_full Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title_fullStr Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title_full_unstemmed Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title_short Analysis of Egg White Protein Composition with Double Nanohole Optical Tweezers
title_sort analysis of egg white protein composition with double nanohole optical tweezers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641915/
https://www.ncbi.nlm.nih.gov/pubmed/31458737
http://dx.doi.org/10.1021/acsomega.8b00651
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