Monica Olvera de la Cruz | |
---|---|
Born | |
Education | UNAM Trinity College, Cambridge |
Known for | soft matter physics electrolytes |
Awards | Presidential Young Investigator Award (1990) National Academy of Sciences Cozzarelli Prize (2007) American Physical Society Polymer Physics Prize (2017) |
Scientific career | |
Fields | Physics, Materials Science and Engineering, Chemistry |
Institutions | Northwestern University |
Doctoral advisor | Sir Sam Edwards |
Doctoral students | Anne M. Mayes |
Website | http://aztec.tech.northwestern.edu |
Monica Olvera de la Cruz is a Mexican born, American and French soft-matter theorist who is the Lawyer Taylor Professor of Materials Science and Engineering and Professor of Chemistry, and by courtesy Professor of Physics and Astronomy and of Chemical and Biological Engineering, at Northwestern University.
Olvera de la Cruz obtained her B.A. in Physics from the UNAM, Mexico, in 1981, and her Ph.D. in Physics from Cambridge University, UK, in 1985. She has been a faculty member at Northwestern University since 1986. From 1995–97, she worked as a Senior Staff Scientist at the Commissariat a l’Energie Atomique, Centre de’Etude, Saclay, France. Olvera de la Cruz is a member of the U.S. National Academy of Sciences [1] as well as the American Philosophical Society [2] and a fellow of the American Academy of Arts and Sciences and the American Physical Society.
She directed the Northwestern Materials Research Center [3] from 2006–2013. She is currently the Director of the Center for Computation and Theory of Soft Materials (CCTSM) at Northwestern University. [4]
Olvera de la Cruz has developed novel methods to analyze complex systems, and in particular molecular electrolytes. She explained the limitations associated with separating long DNA chains via gel electrophoresis dynamics, [5] [6] which was of great importance to the Human Genome Project.
Olvera de la Cruz discovered that counterions induce the precipitation of strongly charged polyelectrolytes by including electrostatic correlations in the analysis. [7] [8] [9] [10] Her work provided a completely revised model of electrostatic effects in complex electrolytes [11] and in dielectrically heterogeneous media. [12] [13]
She has described the emergence of shape and patterns in membranes and in multicomponent complex mixtures. She and her students and postdocs discovered that electrostatics leads to spontaneous symmetry breaking in ionic membranes such as viral capsids [14] (for which they were awarded the 2007 Cozzarelli Prize [15] ) and in fibers. [16] [17]
They also demonstrated the spontaneous emergence of various regular and irregular polyhedral geometries in closed membranes with non-homogeneous elastic properties such as bacterial microcompartments, including carboxysomes, [18] via a mechanism that explains observed shapes in crystalline shells formed by more than one component such as archaea and organelle wall envelopes as well as in ionic vesicles. [19]
By simulating crystals of DNA functionalized nanoparticles with complementary linkers containing both small and large nanoparticles, the Olvera de la Cruz group discovered colloidal crystal “metallicity", [20] [21] whereby small colloids become delocalized within a larger crystal structure. They noted that the transition from the localized to delocalized state is analogous to an insulator-metal transition. Recently, she and her students showed that the localization-delocalization transition is phonon-driven. [22] Additionally, when a localization-delocalization transition is accompanied with a crystal phase transition, it strongly resembles a Peierls transition. [23] This transition is also found in oppositely charged colloidal crystals, [24] resembling sublattice melting in atomic superionics.
Olvera de la Cruz and Qiao found that the binding of the SARS-CoV-2 spike protein receptor-binding domain (RBD) to the human cell receptor hACE2 can be strongly decreased by mutating or blocking the polybasic cleavage site (known as the furin cleavage site), [25] providing a mechanism to decrease COVID 19 infection, as subsequently demonstrated experimentally. [26] [27]
Olvera de la Cruz was on the US Department of Energy's Basic Energy Sciences Advisory Committee from 2012–2022, [40] and has been on the United States National Research Council since 2005. [41] From 2005 to 2008, she was on the Mathematical and Physical Sciences Directorate Advisory Committee of the National Science Foundation. [42] She is on the advisory boards of the Max Planck Institute for Polymer Research in Mainz [43] and the Ecole Supérieure de Physique et Chimie Industrielle de la ville de Paris (ESPCI Paris). [44] She is currently on the editorial board for the Proceedings of the National Academy of Sciences of the United States of America, [45] and is a member of the Gordon Research Conferences' Board of Trustees. [46] She has been a Senior Editor for the journal ACS Central Science (2015–2022). [47]
A colloid is a mixture in which one substance consisting of microscopically dispersed insoluble particles is suspended throughout another substance. Some definitions specify that the particles must be dispersed in a liquid, while others extend the definition to include substances like aerosols and gels. The term colloidal suspension refers unambiguously to the overall mixture. A colloid has a dispersed phase and a continuous phase. The dispersed phase particles have a diameter of approximately 1 nanometre to 1 micrometre.
A capsid is the protein shell of a virus, enclosing its genetic material. It consists of several oligomeric (repeating) structural subunits made of protein called protomers. The observable 3-dimensional morphological subunits, which may or may not correspond to individual proteins, are called capsomeres. The proteins making up the capsid are called capsid proteins or viral coat proteins (VCP). The capsid and inner genome is called the nucleocapsid.
A gel is a semi-solid that can have properties ranging from soft and weak to hard and tough. Gels are defined as a substantially dilute cross-linked system, which exhibits no flow when in the steady state, although the liquid phase may still diffuse through this system.
Polyelectrolytes are polymers whose repeating units bear an electrolyte group. Polycations and polyanions are polyelectrolytes. These groups dissociate in aqueous solutions (water), making the polymers charged. Polyelectrolyte properties are thus similar to both electrolytes (salts) and polymers and are sometimes called polysalts. Like salts, their solutions are electrically conductive. Like polymers, their solutions are often viscous. Charged molecular chains, commonly present in soft matter systems, play a fundamental role in determining structure, stability and the interactions of various molecular assemblies. Theoretical approaches to describe their statistical properties differ profoundly from those of their electrically neutral counterparts, while technological and industrial fields exploit their unique properties. Many biological molecules are polyelectrolytes. For instance, polypeptides, glycosaminoglycans, and DNA are polyelectrolytes. Both natural and synthetic polyelectrolytes are used in a variety of industries.
In physics, a "coffee ring" is a pattern left by a puddle of particle-laden liquid after it evaporates. The phenomenon is named for the characteristic ring-like deposit along the perimeter of a spill of coffee. It is also commonly seen after spilling red wine. The mechanism behind the formation of these and similar rings is known as the coffee ring effect or in some instances, the coffee stain effect, or simply ring stain.
Layer-by-layer (LbL) deposition is a thin film fabrication technique. The films are formed by depositing alternating layers of oppositely charged materials with wash steps in between. This can be accomplished by using various techniques such as immersion, spin, spray, electromagnetism, or fluidics.
A colloidal crystal is an ordered array of colloidal particles and fine grained materials analogous to a standard crystal whose repeating subunits are atoms or molecules. A natural example of this phenomenon can be found in the gem opal, where spheres of silica assume a close-packed locally periodic structure under moderate compression. Bulk properties of a colloidal crystal depend on composition, particle size, packing arrangement, and degree of regularity. Applications include photonics, materials processing, and the study of self-assembly and phase transitions.
Adsorption of polyelectrolytes on solid substrates is a surface phenomenon where long-chained polymer molecules with charged groups bind to a surface that is charged in the opposite polarity. On the molecular level, the polymers do not actually bond to the surface, but tend to "stick" to the surface via intermolecular forces and the charges created by the dissociation of various side groups of the polymer. Because the polymer molecules are so long, they have a large amount of surface area with which to contact the surface and thus do not desorb as small molecules are likely to do. This means that adsorbed layers of polyelectrolytes form a very durable coating. Due to this important characteristic of polyelectrolyte layers they are used extensively in industry as flocculants, for solubilization, as supersorbers, antistatic agents, as oil recovery aids, as gelling aids in nutrition, additives in concrete, or for blood compatibility enhancement to name a few.
Samuel I. Stupp, is a Board of Trustees Professor of Materials Science, Chemistry, and Medicine at Northwestern University in Chicago, IL. He is best known for his work on self-assembling materials and supramolecular chemistry. One of his most notable discoveries is a broad class of peptide amphiphiles that self-assemble into high aspect ratio nanofibers with extensive applications in regenerative medicine. He has also made significant contributions to the fields of supramolecular chemistry, nanotechnology, and organic electronic materials. He has over 500 peer-reviewed publications and was one of the 100 most cited chemists in the 2000–2010 decade.
Polyelectrolytes are charged polymers capable of stabilizing colloidal emulsions through electrostatic interactions. Their effectiveness can be dependent on molecular weight, pH, solvent polarity, ionic strength, and the hydrophilic-lipophilic balance (HLB). Stabilized emulsions are useful in many industrial processes, including deflocculation, drug delivery, petroleum waste treatment, and food technology.
Spherical nucleic acids (SNAs) are nanostructures that consist of a densely packed, highly oriented arrangement of linear nucleic acids in a three-dimensional, spherical geometry. This novel three-dimensional architecture is responsible for many of the SNA's novel chemical, biological, and physical properties that make it useful in biomedicine and materials synthesis. SNAs were first introduced in 1996 by Chad Mirkin’s group at Northwestern University.
Sharon C. Glotzer is an American scientist and "digital alchemist", the Anthony C. Lembke Department Chair of Chemical Engineering, the John Werner Cahn Distinguished University Professor of Engineering and the Stuart W. Churchill Collegiate Professor of Chemical Engineering at the University of Michigan, where she is also professor of materials science and engineering, professor of physics, professor of macromolecular science and engineering, and professor of applied physics. She is recognized for her contributions to the fields of soft matter and computational science, most notably on problems in assembly science and engineering, nanoscience, and the glass transition, for which the elucidation of the nature of dynamical heterogeneity in glassy liquids is of particular significance. She is a member of the National Academy of Sciences, the National Academy of Engineering, and the American Academy of Arts and Sciences.
Double layer forces occur between charged objects across liquids, typically water. This force acts over distances that are comparable to the Debye length, which is on the order of one to a few tenths of nanometers. The strength of these forces increases with the magnitude of the surface charge density. For two similarly charged objects, this force is repulsive and decays exponentially at larger distances, see figure. For unequally charged objects and eventually at shorted distances, these forces may also be attractive. The theory due to Derjaguin, Landau, Verwey, and Overbeek (DLVO) combines such double layer forces together with Van der Waals forces in order to estimate the actual interaction potential between colloidal particles.
Collective motion is defined as the spontaneous emergence of ordered movement in a system consisting of many self-propelled agents. It can be observed in everyday life, for example in flocks of birds, schools of fish, herds of animals and also in crowds and car traffic. It also appears at the microscopic level: in colonies of bacteria, motility assays and artificial self-propelled particles. The scientific community is trying to understand the universality of this phenomenon. In particular it is intensively investigated in statistical physics and in the field of active matter. Experiments on animals, biological and synthesized self-propelled particles, simulations and theories are conducted in parallel to study these phenomena. One of the most famous models that describes such behavior is the Vicsek model introduced by Tamás Vicsek et al. in 1995.
William Michael Gelbart is Distinguished Professor of Chemistry and Biochemistry at the University of California, Los Angeles, and a member of the California NanoSystems Institute and the UCLA Molecular Biology Institute. He obtained his Bachelor of Science degree from Harvard University in 1967, his Master's (1968) and PhD (1970) degrees from the University of Chicago, and did postdoctoral work at the University of Paris (1971) and the University of California, Berkeley (1972). After 30 years of research in theoretical physical chemistry, contributing notably to the fields of gas-phase photophysics, optical properties of simple liquids, and the statistical physics of complex fluids, he started a biophysics laboratory with Charles Knobler in 2002 to investigate the physical aspects of viral infectivity.
Alessio Zaccone is an Italian physicist.
Anne Marie Mayes was an American material science and engineer and a Toyota professor at Massachusetts Institute of Technology (MIT), and MacVicar faculty fellow until 2006. She was the first woman to be promoted from assistant professor to tenured professor in the Department of Materials Science and Engineering at MIT. Mayes focused her research on lithium polymer batteries and the role of polymers in environmental issues. The Anne M. Mayes '86 Fellowship for graduate students at MIT is named in her honor.
Sylvie Roke is a Dutch chemist and physicist specialized in photonics and aqueous systems. As a full professor she holds Julia Jacobi Chair of Photomedicine at EPFL and is the director of the Laboratory for fundamental BioPhotonics.
Hartmut Löwen is a German physicist working in the field of statistical mechanics and soft matter physics.
Barbara Frisken a Canadian physicist who is a professor at the Simon Fraser University. Her research considers soft matter and the realisation of Polymer Electrolyte Membrane Fuel Cells. She was President of the Canadian Association of Physicists.