Evidence map›Paper›PMID 28959404›Full record

ArticleChemical science2017

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

Do-Hyeon Kim, Dong-Kyun Kim, Kai Zhou, Soyeon Park, Yonghoon Kwon, Min Gyu Jeong, Nam Ki Lee, Sung Ho Ryu

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 2 countries.

Do-Hyeon KimDepartment of Life Sciences , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea . Email: sungho@postech.ac.kr.ORCID 0000-0002-0116-7756
Dong-Kyun KimSchool of Interdisciplinary Bioscience and Bioengineering , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea.ORCID 0000-0002-2971-3501
Kai ZhouDepartment of Life Sciences , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea . Email: sungho@postech.ac.kr.ORCID 0000-0003-0685-3533
Soyeon ParkDepartment of Life Sciences , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea . Email: sungho@postech.ac.kr.ORCID 0000-0003-2769-333X
Yonghoon KwonDepartment of Life Sciences , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea . Email: sungho@postech.ac.kr.ORCID 0000-0002-6232-4305
Min Gyu JeongIntegrative Biosciences and Biotechnology , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea.ORCID 0000-0002-2227-6791
Nam Ki LeeSchool of Interdisciplinary Bioscience and Bioengineering , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea.ORCID 0000-0002-6597-555X
Sung Ho RyuDepartment of Life Sciences , Pohang University of Science and Technology , Pohang , 790-784 , Republic of Korea . Email: sungho@postech.ac.kr.ORCID 0000-0003-0913-3048
Pohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Identifiers

PMID28959404
PMCPMC5602156
OpenAlexW2608786543

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.