Quantifying small numbers of antibodies with a 'near-universal' protein-DNA chimera.

Abstract:

:We present general means to greatly increase the sensitivity of antibody-based assays. Augmentation relies on a 'tadpole' protein-DNA chimera whose protein moiety binds most classes of mammalian antibodies but not avian immunoglobulin Y (IgY). We used this tadpole in affinity capture assays followed by real-time PCR to quantify numerous molecules, including prostate-specific antigen (PSA) in human serum, with great sensitivity and accuracy.

journal_name

Nat Methods

journal_title

Nature methods

authors

Burbulis I,Yamaguchi K,Yu R,Resnekov O,Brent R

doi

10.1038/nmeth1127

subject

Has Abstract

pub_date

2007-12-01 00:00:00

pages

1011-3

issue

12

eissn

1548-7091

issn

1548-7105

pii

nmeth1127

journal_volume

4

pub_type

杂志文章
  • Terminal exon characterization with TECtool reveals an abundance of cell-specific isoforms.

    abstract::Sequencing of RNA 3' ends has uncovered numerous sites that do not correspond to the termination sites of known transcripts. Through their 3' untranslated regions, protein-coding RNAs interact with RNA-binding proteins and microRNAs, which regulate many properties, including RNA stability and subcellular localization....

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0114-z

    authors: Gruber AJ,Gypas F,Riba A,Schmidt R,Zavolan M

    更新日期:2018-10-01 00:00:00

  • Single-cell genomics.

    abstract::Methods for genomic analysis at single-cell resolution enable new understanding of complex biological phenomena. Single-cell techniques, ranging from flow cytometry and microfluidics to PCR and sequencing, are used to understand the cellular composition of complex tissues, find new microbial species and perform genome...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth0411-311

    authors: Kalisky T,Quake SR

    更新日期:2011-04-01 00:00:00

  • Imaging cellular network dynamics in three dimensions using fast 3D laser scanning.

    abstract::Spatiotemporal activity patterns in three-dimensionally organized cellular networks are fundamental to the function of the nervous system. Despite advances in functional imaging of cell populations, a method to resolve local network activity in three dimensions has been lacking. Here we introduce a three-dimensional (...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth989

    authors: Göbel W,Kampa BM,Helmchen F

    更新日期:2007-01-01 00:00:00

  • Structural modeling of protein-RNA complexes using crosslinking of segmentally isotope-labeled RNA and MS/MS.

    abstract::Ribonucleoproteins (RNPs) are key regulators of cellular function. We established an efficient approach, crosslinking of segmentally isotope-labeled RNA and tandem mass spectrometry (CLIR-MS/MS), to localize protein-RNA interactions simultaneously at amino acid and nucleotide resolution. The approach was tested on pol...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4235

    authors: Dorn G,Leitner A,Boudet J,Campagne S,von Schroetter C,Moursy A,Aebersold R,Allain FH

    更新日期:2017-05-01 00:00:00

  • Marker-independent identification of glioma-initiating cells.

    abstract::Tumor-initiating cells with stem cell properties are believed to sustain the growth of gliomas, but proposed markers such as CD133 cannot be used to identify these cells with sufficient specificity. We report an alternative isolation method purely based on phenotypic qualities of glioma-initiating cells (GICs), avoidi...

    journal_title:Nature methods

    pub_type: 杂志文章,收录出版

    doi:10.1038/nmeth.1430

    authors: Clément V,Marino D,Cudalbu C,Hamou MF,Mlynarik V,de Tribolet N,Dietrich PY,Gruetter R,Hegi ME,Radovanovic I

    更新日期:2010-03-01 00:00:00

  • Mass spectrometry-based functional proteomics: from molecular machines to protein networks.

    abstract::The study of protein-protein interactions by mass spectrometry is an increasingly important part of post-genomics strategies to understand protein function. A variety of mass spectrometry-based approaches allow characterization of cellular protein assemblies under near-physiological conditions and subsequent assignmen...

    journal_title:Nature methods

    pub_type: 杂志文章,评审

    doi:10.1038/nmeth1093

    authors: Köcher T,Superti-Furga G

    更新日期:2007-10-01 00:00:00

  • Broad specificity profiling of TALENs results in engineered nucleases with improved DNA-cleavage specificity.

    abstract::Although transcription activator-like effector nucleases (TALENs) can be designed to cleave chosen DNA sequences, TALENs have activity against related off-target sequences. To better understand TALEN specificity, we profiled 30 unique TALENs with different target sites, array length and domain sequences for their abil...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2845

    authors: Guilinger JP,Pattanayak V,Reyon D,Tsai SQ,Sander JD,Joung JK,Liu DR

    更新日期:2014-04-01 00:00:00

  • Onco-proteogenomics: cancer proteomics joins forces with genomics.

    abstract::The complexities of tumor genomes are rapidly being uncovered, but how they are regulated into functional proteomes remains poorly understood. Standard proteomics workflows use databases of known proteins, but these databases do not capture the uniqueness of the cancer transcriptome, with its point mutations, unusual ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3138

    authors: Alfaro JA,Sinha A,Kislinger T,Boutros PC

    更新日期:2014-11-01 00:00:00

  • The GEM mapper: fast, accurate and versatile alignment by filtration.

    abstract::Because of ever-increasing throughput requirements of sequencing data, most existing short-read aligners have been designed to focus on speed at the expense of accuracy. The Genome Multitool (GEM) mapper can leverage string matching by filtration to search the alignment space more efficiently, simultaneously deliverin...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2221

    authors: Marco-Sola S,Sammeth M,Guigó R,Ribeca P

    更新日期:2012-12-01 00:00:00

  • Large-scale database searching using tandem mass spectra: looking up the answer in the back of the book.

    abstract::Database searching is an essential element of large-scale proteomics. Because these methods are widely used, it is important to understand the rationale of the algorithms. Most algorithms are based on concepts first developed in SEQUEST and PeptideSearch. Four basic approaches are used to determine a match between a s...

    journal_title:Nature methods

    pub_type: 杂志文章,评审

    doi:10.1038/nmeth725

    authors: Sadygov RG,Cociorva D,Yates JR 3rd

    更新日期:2004-12-01 00:00:00

  • FRETting for a more detailed interactome.

    abstract::A quantitative high-throughput FRET-based method of screening fluorescent protein fusion libraries brings the promise of more detailed interactome maps. ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth0207-112b

    authors: Kaganman I

    更新日期:2007-02-01 00:00:00

  • Localization-based super-resolution imaging meets high-content screening.

    abstract::Single-molecule localization microscopy techniques have proven to be essential tools for quantitatively monitoring biological processes at unprecedented spatial resolution. However, these techniques are very low throughput and are not yet compatible with fully automated, multiparametric cellular assays. This shortcomi...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4486

    authors: Beghin A,Kechkar A,Butler C,Levet F,Cabillic M,Rossier O,Giannone G,Galland R,Choquet D,Sibarita JB

    更新日期:2017-12-01 00:00:00

  • Atmospheric pressure MALDI mass spectrometry imaging of tissues and cells at 1.4-μm lateral resolution.

    abstract::We report an atmospheric pressure (AP) matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) setup with a lateral resolution of 1.4 μm, a mass resolution greater than 100,000, and accuracy below ±2 p.p.m. We achieved this by coupling a focusing objective with a numerical aperture (NA) of ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4071

    authors: Kompauer M,Heiles S,Spengler B

    更新日期:2017-01-01 00:00:00

  • An FDR metric for top-down proteomics.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 评论,杂志文章

    doi:10.1038/s41592-019-0343-9

    authors: Doerr A

    更新日期:2019-03-01 00:00:00

  • Efficient incorporation of unnatural amino acids into proteins in Escherichia coli.

    abstract::We have developed a single-plasmid system for the efficient bacterial expression of mutant proteins containing unnatural amino acids at specific sites designated by amber nonsense codons. In this system, multiple copies of a gene encoding an amber suppressor tRNA derived from a Methanocaldococcus jannaschii tyrosyl-tR...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth864

    authors: Ryu Y,Schultz PG

    更新日期:2006-04-01 00:00:00

  • Induction of linear tracks of DNA double-strand breaks by alpha-particle irradiation of cells.

    abstract::Understanding how cells maintain genome integrity when challenged with DNA double-strand breaks (DSBs) is of major importance, particularly since the discovery of multiple links of DSBs with genome instability and cancer-predisposition disorders. Ionizing radiation is the agent of choice to produce DSBs in cells; howe...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.f.206

    authors: Stap J,Krawczyk PM,Van Oven CH,Barendsen GW,Essers J,Kanaar R,Aten JA

    更新日期:2008-03-01 00:00:00

  • Fast, high-contrast imaging of animal development with scanned light sheet-based structured-illumination microscopy.

    abstract::Recording light-microscopy images of large, nontransparent specimens, such as developing multicellular organisms, is complicated by decreased contrast resulting from light scattering. Early zebrafish development can be captured by standard light-sheet microscopy, but new imaging strategies are required to obtain high-...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1476

    authors: Keller PJ,Schmidt AD,Santella A,Khairy K,Bao Z,Wittbrodt J,Stelzer EH

    更新日期:2010-08-01 00:00:00

  • Rapid selection of transgenic C. elegans using antibiotic resistance.

    abstract::Caenorhabditis elegans is an important model organism in biology, but until now no antibiotic selection markers have been successfully demonstrated for this species. We have developed a selection system using puromycin that allows the rapid and easy isolation of large populations of transgenic worms. This approach is ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1495

    authors: Semple JI,Garcia-Verdugo R,Lehner B

    更新日期:2010-09-01 00:00:00

  • Imaging without lenses: achievements and remaining challenges of wide-field on-chip microscopy.

    abstract::We discuss unique features of lens-free computational imaging tools and report some of their emerging results for wide-field on-chip microscopy, such as the achievement of a numerical aperture (NA) of ∼0.8-0.9 across a field of view (FOV) of more than 20 mm(2) or an NA of ∼0.1 across a FOV of ∼18 cm(2), which correspo...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2114

    authors: Greenbaum A,Luo W,Su TW,Göröcs Z,Xue L,Isikman SO,Coskun AF,Mudanyali O,Ozcan A

    更新日期:2012-09-01 00:00:00

  • Correlated light and electron microscopic imaging of multiple endogenous proteins using Quantum dots.

    abstract::The importance of locating proteins in their context within cells has been heightened recently by the accomplishments in molecular structure and systems biology. Although light microscopy (LM) has been extensively used for mapping protein localization, many studies require the additional resolution of the electron mic...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth791

    authors: Giepmans BN,Deerinck TJ,Smarr BL,Jones YZ,Ellisman MH

    更新日期:2005-10-01 00:00:00

  • The mammalian-membrane two-hybrid assay (MaMTH) for probing membrane-protein interactions in human cells.

    abstract::Cell signaling, one of key processes in both normal cellular function and disease, is coordinated by numerous interactions between membrane proteins that change in response to stimuli. We present a split ubiquitin-based method for detection of integral membrane protein-protein interactions (PPIs) in human cells, terme...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2895

    authors: Petschnigg J,Groisman B,Kotlyar M,Taipale M,Zheng Y,Kurat CF,Sayad A,Sierra JR,Mattiazzi Usaj M,Snider J,Nachman A,Krykbaeva I,Tsao MS,Moffat J,Pawson T,Lindquist S,Jurisica I,Stagljar I

    更新日期:2014-05-01 00:00:00

  • Site-specific recombination in human embryonic stem cells induced by cell-permeant Cre recombinase.

    abstract::The biomedical application of human embryonic stem (hES) cells will increasingly depend on the availability of technologies for highly controlled genetic modification. In mouse genetics, conditional mutagenesis using site-specific recombinases has become an invaluable tool for gain- and loss-of-function studies. Here ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth884

    authors: Nolden L,Edenhofer F,Haupt S,Koch P,Wunderlich FT,Siemen H,Brüstle O

    更新日期:2006-06-01 00:00:00

  • An in vivo multiplexed small-molecule screening platform.

    abstract::Phenotype-based small-molecule screening is a powerful method to identify molecules that regulate cellular functions. However, such screens are generally performed in vitro under conditions that do not necessarily model complex physiological conditions or disease states. Here, we use molecular cell barcoding to enable...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3992

    authors: Grüner BM,Schulze CJ,Yang D,Ogasawara D,Dix MM,Rogers ZN,Chuang CH,McFarland CD,Chiou SH,Brown JM,Cravatt BF,Bogyo M,Winslow MM

    更新日期:2016-10-01 00:00:00

  • Cell surface thermal proteome profiling tracks perturbations and drug targets on the plasma membrane.

    abstract::Numerous drugs and endogenous ligands bind to cell surface receptors leading to modulation of downstream signaling cascades and frequently to adaptation of the plasma membrane proteome. In-depth analysis of dynamic processes at the cell surface is challenging due to biochemical properties and low abundances of plasma ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-020-01022-1

    authors: Kalxdorf M,Günthner I,Becher I,Kurzawa N,Knecht S,Savitski MM,Eberl HC,Bantscheff M

    更新日期:2021-01-01 00:00:00

  • CRISPR off-target analysis in genetically engineered rats and mice.

    abstract::Despite widespread use of CRISPR, comprehensive data on the frequency and impact of Cas9-mediated off-targets in modified rodents are limited. Here we present deep-sequencing data from 81 genome-editing projects on mouse and rat genomes at 1,423 predicted off-target sites, 32 of which were confirmed, and show that hig...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0011-5

    authors: Anderson KR,Haeussler M,Watanabe C,Janakiraman V,Lund J,Modrusan Z,Stinson J,Bei Q,Buechler A,Yu C,Thamminana SR,Tam L,Sowick MA,Alcantar T,O'Neil N,Li J,Ta L,Lima L,Roose-Girma M,Rairdan X,Durinck S,Warming S

    更新日期:2018-07-01 00:00:00

  • Super-resolution imaging in live Caulobacter crescentus cells using photoswitchable EYFP.

    abstract::The commonly used, monomeric EYFP enabled imaging of intracellular protein structures beyond the optical resolution limit ('super-resolution' imaging) in living cells. By combining photoinduced activation of single EYFP fusions and time-lapse imaging, we obtained sub-40 nm resolution images of the filamentous superstr...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1258

    authors: Biteen JS,Thompson MA,Tselentis NK,Bowman GR,Shapiro L,Moerner WE

    更新日期:2008-11-01 00:00:00

  • Highly multiplexed simultaneous detection of RNAs and proteins in single cells.

    abstract::To enable the detection of expression signatures specific to individual cells, we developed PLAYR (proximity ligation assay for RNA), a method for highly multiplexed transcript quantification by flow and mass cytometry that is compatible with standard antibody staining. When used with mass cytometry, PLAYR allowed for...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3742

    authors: Frei AP,Bava FA,Zunder ER,Hsieh EW,Chen SY,Nolan GP,Gherardini PF

    更新日期:2016-03-01 00:00:00

  • The inside tag.

    abstract::An uncharged CoA precursor that can enter the cell is used for covalent, site-specific labeling of proteins inside living cells. ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth1106-872b

    authors: Kaganman I

    更新日期:2006-11-01 00:00:00

  • Automated identification of functional dynamic contact networks from X-ray crystallography.

    abstract::Protein function often depends on the exchange between conformational substates. Allosteric ligand binding or distal mutations can stabilize specific active-site conformations and consequently alter protein function. Observing alternative conformations at low levels of electron density, in addition to comparison of in...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2592

    authors: van den Bedem H,Bhabha G,Yang K,Wright PE,Fraser JS

    更新日期:2013-09-01 00:00:00

  • Large-scale electrophysiology with polymer-based electrodes.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 评论,杂志文章

    doi:10.1038/s41592-019-0315-0

    authors: Vogt N

    更新日期:2019-02-01 00:00:00