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1.
Nat Chem Biol ; 17(6): 724-731, 2021 06.
Artigo em Inglês | MEDLINE | ID: mdl-33820990

RESUMO

Genetically modified microorganisms (GMMs) can enable a wide range of important applications including environmental sensing and responsive engineered living materials. However, containment of GMMs to prevent environmental escape and satisfy regulatory requirements is a bottleneck for real-world use. While current biochemical strategies restrict unwanted growth of GMMs in the environment, there is a need for deployable physical containment technologies to achieve redundant, multi-layered and robust containment. We developed a hydrogel-based encapsulation system that incorporates a biocompatible multilayer tough shell and an alginate-based core. This deployable physical containment strategy (DEPCOS) allows no detectable GMM escape, bacteria to be protected against environmental insults including antibiotics and low pH, controllable lifespan and easy retrieval of genomically recoded bacteria. To highlight the versatility of DEPCOS, we demonstrated that robustly encapsulated cells can execute useful functions, including performing cell-cell communication with other encapsulated bacteria and sensing heavy metals in water samples from the Charles River.


Assuntos
Bactérias/efeitos dos fármacos , Hidrogéis/farmacologia , Alginatos/química , Antibacterianos/farmacologia , Bactérias/genética , Materiais Biocompatíveis , Bioengenharia , DNA Bacteriano/química , DNA Bacteriano/genética , Monitoramento Ambiental , Escherichia coli/efeitos dos fármacos , Escherichia coli/genética , Heme/química , Metais Pesados/química , Organismos Geneticamente Modificados , Percepção de Quorum , Rios , Poluentes da Água/química
2.
J Am Chem Soc ; 136(5): 1992-9, 2014 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-24417287

RESUMO

Lipid vesicle encapsulation is an efficient approach to transfer quantum dots (QDs) into aqueous solutions, which is important for renewable energy applications and biological imaging. However, little is known about the molecular organization at the interface between a QD and lipid membrane. To address this issue, we investigated the properties of 3.0 nm CdSe QDs encapsulated within phospholipid membranes displaying a range of phase transition temperatures (Tm). Theoretical and experimental results indicate that the QD locally alters membrane structure, and in turn, the physical state (phase) of the membrane controls the optical and chemical properties of the QDs. Using photoluminescence, ICP-MS, optical microscopy, and ligand exchange studies, we found that the Tm of the membrane controls optical and chemical properties of lipid vesicle-embedded QDs. Importantly, QDs encapsulated within gel-phase membranes were ultrastable, providing the most photostable non-core/shell QDs in aqueous solution reported to date. Atomistic molecular dynamics simulations support these observations and indicate that membranes are locally disordered displaying greater disordered organization near the particle-solution interface. Using this asymmetry in membrane organization near the particle, we identify a new approach for site-selective modification of QDs by specifically functionalizing the QD surface facing the outer lipid leaflet to generate gold nanoparticle-QD assemblies programmed by Watson-Crick base-pairing.


Assuntos
Compostos de Cádmio/química , Membranas Artificiais , Fosfolipídeos/química , Pontos Quânticos , Compostos de Selênio/química , DNA de Cadeia Simples/química , Ouro/química , Ligantes , Luminescência , Microscopia Eletrônica de Transmissão , Simulação de Dinâmica Molecular , Oxirredução , Transição de Fase , Processos Fotoquímicos , Propriedades de Superfície
3.
ACS Macro Lett ; 11(9): 1156-1161, 2022 Sep 20.
Artigo em Inglês | MEDLINE | ID: mdl-36069541

RESUMO

Photoinduced electron/energy transfer (PET)-reversible addition-fragmentation chain transfer polymerization (RAFT) and conventional photoinitiated RAFT were used to synthesize polymer networks. In this study, two different metal catalysts, namely, tris[2-phenylpyridinato-C2,N]iridium(III) (Ir(ppy)3) and zinc tetraphenylporphyrin (ZnTPP), were selected to generate two different catalytic pathways, one with Ir(ppy)3 proceeding through an energy-transfer pathway and one with ZnTPP proceeding through an electron-transfer pathway. These PET-RAFT systems were contrasted against a conventional photoinitated RAFT process. Mechanically robust materials were generated. Using bulk swelling ratios and degradable cross-linkers, the homogeneity of the networks was evaluated. Especially at high primary chain length and cross-link density, the PET-RAFT systems generated more uniform networks than those made by conventional RAFT, with the electron transfer-based ZnTPP giving superior results to those of Ir(ppy)3. The ability to deactivate radicals either by RAFT exchange or reversible coupling in PET RAFT was proposed as the mechanism that gave better control in PET-RAFT systems.


Assuntos
Irídio , Polímeros , Transferência de Energia , Metaloporfirinas
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