Advanced Science · 2023 · 10 citations · 26 references
Life SciencesBiochemistryBiophysicsMembrane BiochemistryMembrane BiophysicsProtein EngineeringBiological MembranesMacromolecular AssemblyMembrane Phase BehaviorMembrane ProteinsMembrane Self-assemblyVesicle FormationCoacervate FormationDisordered Membrane PhasesLiquid - Liquid Phase SeparationLiquid-liquid Phase SeparationMembrane Phase SeparationPhase Separation Of Intrinsically Disordered ProteinsPhase Transition DynamicsPhase Transitions In Biomembranes
Numerous biological systems contain vesicle-like biomolecular compartments without membranes, which contribute to diverse functions including gene regulation, stress response, signaling, and skin barrier formation. Coacervation, as a form of liquid-liquid phase separation (LLPS), is recognized as a representative precursor to the formation and assembly of membrane-less vesicle-like structures, although their formation mechanism remains unclear. In this study, a coacervation-driven membrane-less vesicle-like structure is constructed using two proteins, GG1234 (an anionic intrinsically disordered protein) and bhBMP-2 (a bioengineered human bone morphogenetic protein 2). GG1234 formed both simple coacervates by itself and complex coacervates with the relatively cationic bhBMP-2 under acidic conditions. Upon addition of dissolved bhBMP-2 to the simple coacervates of GG1234, a phase transition from spherical simple coacervates to vesicular condensates occurred via the interactions between GG1234 and bhBMP-2 on the surface of the highly viscoelastic GG1234 simple coacervates. Furthermore, the shell structure in the outer region of the GG1234/bhBMP-2 vesicular condensates exhibited gel-like properties, leading to the formation of multiphasic vesicle-like compartments. A potential mechanism is proposed for the formation of the membrane-less GG1234/bhBMP-2 vesicle-like compartments. This study provides a dynamic process underlying the formation of biomolecular multiphasic condensates, thereby enhancing the understanding of these biomolecular structures.
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Highly accurate protein structure prediction with AlphaFold
John Jumper, Alexander Pritzel, Tim Green et al. · Nature · 2021 · 45.2K citations · Full text
The Amino Acid Sequence of Egg White Lysozyme
Robert E. Canfield · Journal of Biological Chemistry · 1963 · 737 citations · Full text
Life Sciences, Biochemistry, Biology +11