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1.
Proc Natl Acad Sci U S A ; 111(7): 2425-30, 2014 Feb 18.
Artículo en Inglés | MEDLINE | ID: mdl-24469792

RESUMEN

Membrane proteins are generally divided into two classes. Integral proteins span the lipid bilayer, and peripheral proteins are located at the membrane surface. Here, we provide evidence for membrane proteins of a third class that stabilize lipid pores, most probably as toroidal structures. We examined mutants of the staphylococcal α-hemolysin pore so severely truncated that the protein cannot span a bilayer. Nonetheless, the doughnut-like structures elicited well-defined transmembrane ionic currents by inducing pore formation in the underlying lipids. The formation of lipid pores, produced here by a structurally defined protein, is supported by the lipid and voltage dependences of pore formation, and by molecular dynamics simulations. We discuss the role of stabilized lipid pores in amyloid disease, the action of antimicrobial peptides, and the assembly of the membrane-attack complexes of the immune system.


Asunto(s)
Permeabilidad de la Membrana Celular/fisiología , Membrana Dobles de Lípidos/química , Proteínas de la Membrana/química , Modelos Moleculares , Conformación Proteica , Toxinas Bacterianas/química , Toxinas Bacterianas/metabolismo , Proteínas Hemolisinas/química , Proteínas Hemolisinas/metabolismo , Membrana Dobles de Lípidos/metabolismo , Proteínas de la Membrana/clasificación , Proteínas de la Membrana/metabolismo , Simulación de Dinámica Molecular , Mutagénesis , Reacción en Cadena de la Polimerasa
2.
Nanotechnology ; 26(8): 084002, 2015 Feb 27.
Artículo en Inglés | MEDLINE | ID: mdl-25648138

RESUMEN

In nanopore sequencing, where single DNA strands are electrophoretically translocated through a nanopore and the resulting ionic signal is used to identify the four DNA bases, an enzyme has been used to ratchet the nucleic acid stepwise through the pore at a controlled speed. In this work, we investigated the ability of alpha-hemolysin nanopores to distinguish the four DNA bases under conditions that are compatible with the activity of DNA-handling enzymes. Our findings suggest that in immobilized strands, the applied potential exerts a force on DNA (∼10 pN at +160 mV) that increases the distance between nucleobases by about 2.2 ŠV(-1). The four nucleobases can be resolved over wide ranges of applied potentials (from +60 to +220 mV in 1 m KCl) and ionic strengths (from 200 mM KCl to 1 M KCl at +160 mV) and nucleobase recognition can be improved when the ionic strength on the side of the DNA-handling enzyme is low, while the ionic strength on the opposite side is high.


Asunto(s)
ADN/química , Análisis de Secuencia de ADN/métodos , Electricidad , Concentración de Iones de Hidrógeno , Iones , Nanoporos , Estrés Mecánico
3.
Proc Natl Acad Sci U S A ; 106(19): 7702-7, 2009 May 12.
Artículo en Inglés | MEDLINE | ID: mdl-19380741

RESUMEN

The sequencing of individual DNA strands with nanopores is under investigation as a rapid, low-cost platform in which bases are identified in order as the DNA strand is transported through a pore under an electrical potential. Although the preparation of solid-state nanopores is improving, biological nanopores, such as alpha-hemolysin (alphaHL), are advantageous because they can be precisely manipulated by genetic modification. Here, we show that the transmembrane beta-barrel of an engineered alphaHL pore contains 3 recognition sites that can be used to identify all 4 DNA bases in an immobilized single-stranded DNA molecule, whether they are located in an otherwise homopolymeric DNA strand or in a heteropolymeric strand. The additional steps required to enable nanopore DNA sequencing are outlined.


Asunto(s)
ADN/genética , Nanotecnología/métodos , Oligonucleótidos/genética , Análisis de Secuencia de ADN/métodos , Animales , Secuencia de Bases , ADN de Cadena Simple/genética , Genómica , Proteínas Hemolisinas/genética , Datos de Secuencia Molecular , Nanopartículas/química , Nanoestructuras , Ingeniería de Proteínas/métodos , Conejos , Análisis de Secuencia de ADN/instrumentación , Homología de Secuencia de Ácido Nucleico
4.
Nat Biotechnol ; 40(10): 1488-1499, 2022 10.
Artículo en Inglés | MEDLINE | ID: mdl-35637420

RESUMEN

High-order three-dimensional (3D) interactions between more than two genomic loci are common in human chromatin, but their role in gene regulation is unclear. Previous high-order 3D chromatin assays either measure distant interactions across the genome or proximal interactions at selected targets. To address this gap, we developed Pore-C, which combines chromatin conformation capture with nanopore sequencing of concatemers to profile proximal high-order chromatin contacts at the genome scale. We also developed the statistical method Chromunity to identify sets of genomic loci with frequencies of high-order contacts significantly higher than background ('synergies'). Applying these methods to human cell lines, we found that synergies were enriched in enhancers and promoters in active chromatin and in highly transcribed and lineage-defining genes. In prostate cancer cells, these included binding sites of androgen-driven transcription factors and the promoters of androgen-regulated genes. Concatemers of high-order contacts in highly expressed genes were demethylated relative to pairwise contacts at the same loci. Synergies in breast cancer cells were associated with tyfonas, a class of complex DNA amplicons. These results rigorously link genome-wide high-order 3D interactions to lineage-defining transcriptional programs and establish Pore-C and Chromunity as scalable approaches to assess high-order genome structure.


Asunto(s)
Secuenciación de Nanoporos , Nanoporos , Andrógenos , Cromatina/genética , Humanos , Factores de Transcripción/genética
5.
Nano Lett ; 10(9): 3633-7, 2010 Sep 08.
Artículo en Inglés | MEDLINE | ID: mdl-20704324

RESUMEN

Nanopores are under investigation for single-molecule DNA sequencing. The alpha-hemolysin (alphaHL) protein nanopore contains three recognition points capable of nucleobase discrimination in individual immobilized ssDNA molecules. We have modified the recognition point R(1) by extensive mutagenesis of residue 113. Amino acids that provide an energy barrier to ion flow (e.g., bulky or hydrophobic residues) strengthen base identification, while amino acids that lower the barrier weaken it. Amino acids with related side chains produce similar patterns of nucleobase recognition providing a rationale for the redesign of recognition points.


Asunto(s)
ADN de Cadena Simple/química , Proteínas Hemolisinas/química , Sustitución de Aminoácidos , Secuencia de Bases , Modelos Moleculares , Mutagénesis
6.
Genes (Basel) ; 12(1)2021 01 16.
Artículo en Inglés | MEDLINE | ID: mdl-33467183

RESUMEN

For the past two decades, microbial monitoring of the International Space Station (ISS) has relied on culture-dependent methods that require return to Earth for analysis. This has a number of limitations, with the most significant being bias towards the detection of culturable organisms and the inherent delay between sample collection and ground-based analysis. In recent years, portable and easy-to-use molecular-based tools, such as Oxford Nanopore Technologies' MinION™ sequencer and miniPCR bio's miniPCR™ thermal cycler, have been validated onboard the ISS. Here, we report on the development, validation, and implementation of a swab-to-sequencer method that provides a culture-independent solution to real-time microbial profiling onboard the ISS. Method development focused on analysis of swabs collected in a low-biomass environment with limited facility resources and stringent controls on allowed processes and reagents. ISS-optimized procedures included enzymatic DNA extraction from a swab tip, bead-based purifications, altered buffers, and the use of miniPCR and the MinION. Validation was conducted through extensive ground-based assessments comparing current standard culture-dependent and newly developed culture-independent methods. Similar microbial distributions were observed between the two methods; however, as expected, the culture-independent data revealed microbial profiles with greater diversity. Protocol optimization and verification was established during NASA Extreme Environment Mission Operations (NEEMO) analog missions 21 and 22, respectively. Unique microbial profiles obtained from analog testing validated the swab-to-sequencer method in an extreme environment. Finally, four independent swab-to-sequencer experiments were conducted onboard the ISS by two crewmembers. Microorganisms identified from ISS swabs were consistent with historical culture-based data, and primarily consisted of commonly observed human-associated microbes. This simplified method has been streamlined for high ease-of-use for a non-trained crew to complete in an extreme environment, thereby enabling environmental and human health diagnostics in real-time as future missions take us beyond low-Earth orbit.


Asunto(s)
Bacterias/genética , ADN Bacteriano/genética , Secuenciación de Nanoporos , Análisis de Secuencia de ADN , Nave Espacial , Manejo de Especímenes , Humanos
7.
Genes (Basel) ; 11(1)2020 01 09.
Artículo en Inglés | MEDLINE | ID: mdl-31936690

RESUMEN

The MinION sequencer has made in situ sequencing feasible in remote locations. Following our initial demonstration of its high performance off planet with Earth-prepared samples, we developed and tested an end-to-end, sample-to-sequencer process that could be conducted entirely aboard the International Space Station (ISS). Initial experiments demonstrated the process with a microbial mock community standard. The DNA was successfully amplified, primers were degraded, and libraries prepared and sequenced. The median percent identities for both datasets were 84%, as assessed from alignment of the mock community. The ability to correctly identify the organisms in the mock community standard was comparable for the sequencing data obtained in flight and on the ground. To validate the process on microbes collected from and cultured aboard the ISS, bacterial cells were selected from a NASA Environmental Health Systems Surface Sample Kit contact slide. The locations of bacterial colonies chosen for identification were labeled, and a small number of cells were directly added as input into the sequencing workflow. Prepared DNA was sequenced, and the data were downlinked to Earth. Return of the contact slide to the ground allowed for standard laboratory processing for bacterial identification. The identifications obtained aboard the ISS, Staphylococcus hominis and Staphylococcus capitis, matched those determined on the ground down to the species level. This marks the first ever identification of microbes entirely off Earth, and this validated process could be used for in-flight microbial identification, diagnosis of infectious disease in a crewmember, and as a research platform for investigators around the world.


Asunto(s)
Secuenciación de Nanoporos/métodos , ARN Ribosómico 16S/genética , Manejo de Especímenes/métodos , Bacterias/genética , ADN Bacteriano/genética , ADN Ribosómico/genética , Exobiología/métodos , Medio Ambiente Extraterrestre , Genoma Bacteriano/genética , Microbiota/genética , Nanoporos , Análisis de Secuencia de ADN/métodos , Nave Espacial/instrumentación
8.
bioRxiv ; 2020 Sep 04.
Artículo en Inglés | MEDLINE | ID: mdl-32908977

RESUMEN

Genome sequencing has been widely deployed to study the evolution of SARS-CoV-2 with more than 90,000 genome sequences uploaded to the GISAID database. We published a method for SARS-CoV-2 genome sequencing (https://www.protocols.io/view/ncov-2019-sequencing-protocol-bbmuik6w) online on January 22, 2020. This approach has rapidly become the most popular method for sequencing SARS-CoV-2 due to its simplicity and cost-effectiveness. Here we present improvements to the original protocol: i) an updated primer scheme with 22 additional primers to improve genome coverage, ii) a streamlined library preparation workflow which improves demultiplexing rate for up to 96 samples and reduces hands-on time by several hours and iii) cost savings which bring the reagent cost down to £10 per sample making it practical for individual labs to sequence thousands of SARS-CoV-2 genomes to support national and international genomic epidemiology efforts.

9.
Nat Biotechnol ; 36(4): 321-323, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29553574

RESUMEN

The human genome reference sequence remains incomplete owing to the challenge of assembling long tracts of near-identical tandem repeats in centromeres. We implemented a nanopore sequencing strategy to generate high-quality reads that span hundreds of kilobases of highly repetitive DNA in a human Y chromosome centromere. Combining these data with short-read variant validation, we assembled and characterized the centromeric region of a human Y chromosome.


Asunto(s)
Centrómero/genética , Cromosomas Humanos Y/genética , Secuenciación de Nucleótidos de Alto Rendimiento , Secuencias Repetidas en Tándem/genética , Genoma Humano/genética , Humanos , Nanoporos , Secuencias Repetitivas de Ácidos Nucleicos/genética
10.
N Biotechnol ; 33(3): 311-30, 2016 May 25.
Artículo en Inglés | MEDLINE | ID: mdl-26514324

RESUMEN

The REvolutionary Approaches and Devices for Nucleic Acid analysis (READNA) project received funding from the European Commission for 41/2 years. The objectives of the project revolved around technological developments in nucleic acid analysis. The project partners have discovered, created and developed a huge body of insights into nucleic acid analysis, ranging from improvements and implementation of current technologies to the most promising sequencing technologies that constitute a 3(rd) and 4(th) generation of sequencing methods with nanopores and in situ sequencing, respectively.


Asunto(s)
Biotecnología/métodos , ADN/análisis , ADN/genética , Animales , Química Clic , Exoma/genética , Humanos , Espectrometría de Masas , Análisis de Secuencia de ADN
12.
ACS Nano ; 9(8): 7895-903, 2015 Aug 25.
Artículo en Inglés | MEDLINE | ID: mdl-26114210

RESUMEN

The α-hemolysin (αHL) protein nanopore has been investigated previously as a base detector for the strand sequencing of DNA and RNA. Recent findings have suggested that shorter pores might provide improved base discrimination. New work has also shown that truncated-barrel mutants (TBM) of αHL form functional pores in lipid bilayers. Therefore, we tested TBM pores for the ability to recognize bases in DNA strands immobilized within them. In the case of TBMΔ6, in which the barrel is shortened by ∼16 Å, one of the three recognition sites found in the wild-type pore, R1, was almost eliminated. With further mutagenesis (Met113 → Gly), R1 was completely removed, demonstrating that TBM pores can mediate sharpened recognition. Remarkably, a second mutant of TBMΔ6 (Met113 → Phe) was able to bind the positively charged ß-cyclodextrin, am7ßCD, unusually tightly, permitting the continuous recognition of individual nucleoside monophosphates, which would be required for exonuclease sequencing mediated by nanopore base identification.


Asunto(s)
Adenina/análisis , Técnicas Biosensibles , Proteínas Hemolisinas/química , Poli C/análisis , Porinas/química , Adenina/química , Sustitución de Aminoácidos , Secuencia de Bases , Proteínas Hemolisinas/genética , Membrana Dobles de Lípidos/química , Modelos Moleculares , Datos de Secuencia Molecular , Mycobacterium smegmatis/química , Nanoporos/ultraestructura , Mutación Puntual , Poli C/química , Porinas/genética , Estructura Secundaria de Proteína , Estructura Terciaria de Proteína , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Electricidad Estática , beta-Ciclodextrinas/química
13.
Structure ; 21(10): 1743-56, 2013 Oct 08.
Artículo en Inglés | MEDLINE | ID: mdl-24035709

RESUMEN

The human extracellular matrix glycoprotein fibrillin-1 is the primary component of the 10- to 12-nm-diameter microfibrils, which perform key structural and regulatory roles in connective tissues. Relatively little is known about the molecular mechanisms of fibrillin assembly into microfibrils. Studies using recombinant fibrillin fragments indicate that an interaction between the N- and C-terminal regions drives head-to-tail assembly. Here, we present the structure of a fibrillin N-terminal fragment comprising the fibrillin unique N-terminal (FUN) and the first three epidermal growth factor (EGF)-like domains (FUN-EGF3). Two rod-like domain pairs are separated by a short, flexible linker between the EGF1 and EGF2 domains. We also show that the binding site for the C-terminal region spans multiple domains and overlaps with a heparin interaction site. These data suggest that heparan sulfate may sequester fibrillin at the cell surface via FUN-EGF3 prior to aggregation of the C terminus, thereby regulating microfibril assembly.


Asunto(s)
Heparitina Sulfato/química , Microfibrillas/química , Proteínas de Microfilamentos/química , Secuencia de Aminoácidos , Secuencia Conservada , Fibrilina-1 , Fibrilinas , Humanos , Enlace de Hidrógeno , Modelos Moleculares , Datos de Secuencia Molecular , Resonancia Magnética Nuclear Biomolecular , Unión Proteica , Dominios y Motivos de Interacción de Proteínas , Multimerización de Proteína , Estructura Secundaria de Proteína
14.
Methods Enzymol ; 475: 591-623, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20627172

RESUMEN

We describe the methods used in our laboratory for the analysis of single nucleic acid molecules with protein nanopores. The technical section is preceded by a review of the variety of experiments that can be done with protein nanopores. The end goal of much of this work is single-molecule DNA sequencing, although sequencing is not discussed explicitly here. The technical section covers the equipment required for nucleic acid analysis, the preparation and storage of the necessary materials, and aspects of signal processing and data analysis.


Asunto(s)
Nanotecnología , Ácidos Nucleicos/química , Proteínas/química , Porosidad
15.
Chem Commun (Camb) ; 46(43): 8195-7, 2010 Nov 21.
Artículo en Inglés | MEDLINE | ID: mdl-20927439

RESUMEN

Two DNA bases, 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (hmC), marks of epigenetic modification, are recognized in immobilized DNA strands and distinguished from G, A, T and C by nanopore current recording. Therefore, if further aspects of nanopore sequencing can be addressed, the approach will provide a means to locate epigenetic modifications in unamplified genomic DNA.


Asunto(s)
5-Metilcitosina/química , Citosina/análogos & derivados , ADN/química , Proteínas Hemolisinas/química , Nanoporos , Ciclodextrinas/química , Citosina/química , Epigénesis Genética
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