Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Cells ; 9(6)2020 06 09.
Article in English | MEDLINE | ID: mdl-32527013

ABSTRACT

Cortical actomyosin flows, among other mechanisms, scale up spontaneous symmetry breaking and thus play pivotal roles in cell differentiation, division, and motility. According to many model systems, myosin motor-induced local contractions of initially isotropic actomyosin cortices are nucleation points for generating cortical flows. However, the positive feedback mechanisms by which spontaneous contractions can be amplified towards large-scale directed flows remain mostly speculative. To investigate such a process on spherical surfaces, we reconstituted and confined initially isotropic minimal actomyosin cortices to the interfaces of emulsion droplets. The presence of ATP leads to myosin-induced local contractions that self-organize and amplify into directed large-scale actomyosin flows. By combining our experiments with theory, we found that the feedback mechanism leading to a coordinated directional motion of actomyosin clusters can be described as asymmetric cluster vibrations, caused by intrinsic non-isotropic ATP consumption with spatial confinement. We identified fingerprints of vibrational states as the basis of directed motions by tracking individual actomyosin clusters. These vibrations may represent a generic key driver of directed actomyosin flows under spatial confinement in vitro and in living systems.


Subject(s)
Actomyosin/metabolism , Cell Movement , Humans
2.
Chembiochem ; 21(15): 2149-2160, 2020 08 03.
Article in English | MEDLINE | ID: mdl-32187828

ABSTRACT

Light-driven ATP regeneration systems combining ATP synthase and bacteriorhodopsin have been proposed as an energy supply in the field of synthetic biology. Energy is required to power biochemical reactions within artificially created reaction compartments like protocells, which are typically based on either lipid or polymer membranes. The insertion of membrane proteins into different hybrid membranes is delicate, and studies comparing these systems with liposomes are needed. Here we present a detailed study of membrane protein functionality in different hybrid compartments made of graft polymer PDMS-g-PEO and diblock copolymer PBd-PEO. Activity of more than 90 % in lipid/polymer-based hybrid vesicles could prove an excellent biocompatibility. A significant enhancement of long-term stability (80 % remaining activity after 42 days) could be demonstrated in polymer/polymer-based hybrids.


Subject(s)
Adenosine Triphosphate/biosynthesis , Light , Adenosine Triphosphate/metabolism , Bacillus/cytology , Bacillus/metabolism , Bacillus/radiation effects , Cell Membrane/metabolism , Cell Membrane/radiation effects , Dimethylpolysiloxanes/chemistry , Nylons/chemistry , Permeability/radiation effects , Polyethylene Glycols/chemistry
3.
Adv Biosyst ; 3(6): e1800320, 2019 06.
Article in English | MEDLINE | ID: mdl-32648706

ABSTRACT

The ability of designing biosynthetic systems with well-defined functional biomodules from scratch is an ambitious and revolutionary goal to deliver innovative, engineered solutions to future challenges in biotechnology and process systems engineering. In this work, several key challenges including modularization, functional biomodule identification, and assembly are discussed. In addition, an in silico protocell modeling approach is presented as a foundation for a computational model-based toolkit for rational analysis and modular design of biomimetic systems.


Subject(s)
Artificial Cells/chemistry , Biomimetic Materials/chemistry , Synthetic Biology
4.
Langmuir ; 34(19): 5435-5443, 2018 05 15.
Article in English | MEDLINE | ID: mdl-29718667

ABSTRACT

The design of efficient schemes for nicotinamide adenine dinucleotide (NAD) regeneration is essential for the development of enzymatic biotechnological processes in order to sustain continuous production. In line with our motivation for the encapsulation of redox cascades in liposomes to serve as microbioreactors, we developed a straightforward strategy for the interfacial oxidation of entrapped NADH by ferricyanide as an external electron acceptor. Instead of the commonly applied enzymatic regeneration methods, we employed a hydrophobic redox shuttle embedded in the liposome bilayer. Tetracyanoquinodimethane (TCNQ) mediated electron transfer across the membrane and thus allowed us to shortcut and emulate part of the electron transfer chain functionality without the involvement of membrane proteins. To describe the experimental system, we developed a mathematical model which allowed for the determination of rate constants and exhibited handy predictive utility.


Subject(s)
Biotechnology/methods , Liposomes/chemistry , NAD/metabolism , Nitriles/chemistry , Electron Transport , Models, Theoretical , NAD/chemistry , Oxidation-Reduction
SELECTION OF CITATIONS
SEARCH DETAIL
...