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Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell

Cellular processes occur through the orchestration of multi-step molecular reactions. Reaction progress kinetic analysis (RPKA) can provide the mechanistic details to elucidate the multi-step molecular reactions. However, current tools have limited ability to simultaneously monitor dynamic variation...

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Autores principales: Kim, Do-Hyeon, Kim, Dong-Kyun, Zhou, Kai, Park, Soyeon, Kwon, Yonghoon, Jeong, Min Gyu, Lee, Nam Ki, Ryu, Sung Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602156/
https://www.ncbi.nlm.nih.gov/pubmed/28959404
http://dx.doi.org/10.1039/c7sc01159h
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author Kim, Do-Hyeon
Kim, Dong-Kyun
Zhou, Kai
Park, Soyeon
Kwon, Yonghoon
Jeong, Min Gyu
Lee, Nam Ki
Ryu, Sung Ho
author_facet Kim, Do-Hyeon
Kim, Dong-Kyun
Zhou, Kai
Park, Soyeon
Kwon, Yonghoon
Jeong, Min Gyu
Lee, Nam Ki
Ryu, Sung Ho
author_sort Kim, Do-Hyeon
collection PubMed
description Cellular processes occur through the orchestration of multi-step molecular reactions. Reaction progress kinetic analysis (RPKA) can provide the mechanistic details to elucidate the multi-step molecular reactions. However, current tools have limited ability to simultaneously monitor dynamic variations in multiple complex states at the single molecule level to apply RPKA in living cells. In this research, a single particle tracking-based reaction progress kinetic analysis (sptRPKA) was developed to simultaneously determine the kinetics of multiple states of protein complexes in the membrane of a single living cell. The subpopulation ratios of different states were quantitatively (and statistically) reliably extracted from the diffusion coefficient distribution rapidly acquired by single particle tracking at constant and high density over a long period of time using super-resolution microscopy. Using sptRPKA, a series of molecular mechanisms of epidermal growth factor receptor (EGFR) cellular processing induced by cetuximab were investigated. By comprehensively measuring the rate constants and cooperativity of the molecular reactions involving four EGFR complex states, a previously unknown intermediate state was identified that represents the rate limiting step responsible for the selectivity of cetuximab-induced EGFR endocytosis to cancer cells.
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spelling pubmed-56021562017-09-28 Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell Kim, Do-Hyeon Kim, Dong-Kyun Zhou, Kai Park, Soyeon Kwon, Yonghoon Jeong, Min Gyu Lee, Nam Ki Ryu, Sung Ho Chem Sci Chemistry Cellular processes occur through the orchestration of multi-step molecular reactions. Reaction progress kinetic analysis (RPKA) can provide the mechanistic details to elucidate the multi-step molecular reactions. However, current tools have limited ability to simultaneously monitor dynamic variations in multiple complex states at the single molecule level to apply RPKA in living cells. In this research, a single particle tracking-based reaction progress kinetic analysis (sptRPKA) was developed to simultaneously determine the kinetics of multiple states of protein complexes in the membrane of a single living cell. The subpopulation ratios of different states were quantitatively (and statistically) reliably extracted from the diffusion coefficient distribution rapidly acquired by single particle tracking at constant and high density over a long period of time using super-resolution microscopy. Using sptRPKA, a series of molecular mechanisms of epidermal growth factor receptor (EGFR) cellular processing induced by cetuximab were investigated. By comprehensively measuring the rate constants and cooperativity of the molecular reactions involving four EGFR complex states, a previously unknown intermediate state was identified that represents the rate limiting step responsible for the selectivity of cetuximab-induced EGFR endocytosis to cancer cells. Royal Society of Chemistry 2017-07-01 2017-04-24 /pmc/articles/PMC5602156/ /pubmed/28959404 http://dx.doi.org/10.1039/c7sc01159h Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Kim, Do-Hyeon
Kim, Dong-Kyun
Zhou, Kai
Park, Soyeon
Kwon, Yonghoon
Jeong, Min Gyu
Lee, Nam Ki
Ryu, Sung Ho
Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title_full Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title_fullStr Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title_full_unstemmed Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title_short Single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced EGFR processes in a single living cell
title_sort single particle tracking-based reaction progress kinetic analysis reveals a series of molecular mechanisms of cetuximab-induced egfr processes in a single living cell
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602156/
https://www.ncbi.nlm.nih.gov/pubmed/28959404
http://dx.doi.org/10.1039/c7sc01159h
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