Evidence map›Paper›PMID 37745461›Full record

ArticlebioRxiv : the preprint server for biology2023

Robust and scalable single-molecule protein sequencing with fluorosequencing.

James H Mapes, Julia Stover, Heather D Stout, Tucker M Folsom, Emily Babcock, Sandra Loudwig, Christopher Martin, Mariah J Austin, Fan Tu, Casey J Howdieshell and 12 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

22 authors.

James H MapesErisyon, Inc. Austin, TX, 78752.
Julia StoverErisyon, Inc. Austin, TX, 78752.
Heather D StoutErisyon, Inc. Austin, TX, 78752.ORCID 0000-0001-8541-5587
Tucker M FolsomErisyon, Inc. Austin, TX, 78752.ORCID 0000-0002-9693-6393
Emily BabcockErisyon, Inc. Austin, TX, 78752.
Sandra LoudwigErisyon, Inc. Austin, TX, 78752.
Christopher MartinErisyon, Inc. Austin, TX, 78752.
Mariah J AustinErisyon, Inc. Austin, TX, 78752.
Fan TuDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712.ORCID 0000-0002-5673-5300
Casey J HowdieshellErisyon, Inc. Austin, TX, 78752.
Zachary B SimpsonErisyon, Inc. Austin, TX, 78752.
Thomas BlomErisyon, Inc. Austin, TX, 78752.
Daniel WeaverErisyon, Inc. Austin, TX, 78752.
Daniel WinklerErisyon, Inc. Austin, TX, 78752.
Kent Vander VeldenErisyon, Inc. Austin, TX, 78752.
Parham M OssarehErisyon, Inc. Austin, TX, 78752.
John M BeierleButterfly Biotech Consulting, Carlsbad, CA.
Talli SomekhErisyon, Inc. Austin, TX, 78752.
Angela M BardoErisyon, Inc. Austin, TX, 78752.ORCID 0000-0002-6637-4748
Eric V AnslynDepartment of Chemistry, The University of Texas at Austin, Austin, TX 78712.ORCID 0000-0002-5137-8797
Edward M MarcotteDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712.ORCID 0000-0001-8808-180X
Jagannath SwaminathanErisyon, Inc. Austin, TX, 78752.ORCID 0000-0002-5005-7182

Funding

Proteomics and model organism humanization to decode human geneticsR35GM122480 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI EDWARD M MARCOTTE · 2017 to 2026
$5.4M
NIGMS NIH HHS R35 GM122480
6 · The paper itself

Abstract

The need to accurately survey proteins and their modifications with ever higher sensitivities, particularly in clinical settings with limited samples, is spurring development of new single molecule proteomics technologies. Fluorosequencing is one such highly parallelized single molecule peptide sequencing platform, based on determining the sequence positions of select amino acid types within peptides to enable their identification and quantification from a reference database. Here, we describe substantial improvements to fluorosequencing, including identifying fluorophores compatible with the sequencing chemistry, mitigating dye-dye interactions through the use of extended polyproline linkers, and developing an end-to-end workflow for sample preparation and sequencing. We demonstrate by fluorosequencing peptides in mixtures and identifying a target neoantigen from a database of decoy MHC peptides, highlighting the potential of the technology for high sensitivity clinical applications.

Indexed as

amino acid sequencesfluorosequencingpeptide labelingproteomicssingle-molecule protein sequencingtotal internal reflectance fluorescence microscopy

Identifiers

PMID37745461
PMCPMC10516020

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.