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Pasadena, CA, United States

The California Institute of Technology is a private research university located in Pasadena, California, United States. Caltech has six academic divisions with strong emphasis on science and engineering. Its 124-acre primary campus is located approximately 11 mi northeast of downtown Los Angeles.Although founded as a preparatory and vocational school by Amos G. Throop in 1891, the college attracted influential scientists such as George Ellery Hale, Arthur Amos Noyes, and Robert Andrews Millikan in the early 20th century. The vocational and preparatory schools were disbanded and spun off in 1910, and the college assumed its present name in 1921. In 1934, Caltech was elected to the Association of American Universities, and the antecedents of NASA's Jet Propulsion Laboratory, which Caltech continues to manage and operate, were established between 1936 and 1943 under Theodore von Kármán. The university is one among a small group of Institutes of Technology in the United States which tends to be primarily devoted to the instruction of technical arts and applied science.Despite its small size, 33 Caltech alumni and faculty have won a total of 34 Nobel Prizes and 71 have won the United States National Medal of Science or Technology. There are 112 faculty members who have been elected to the National Academies. In addition, numerous faculty members are associated with the Howard Hughes Medical Institute as well as NASA. Caltech managed $332 million in 2011 in sponsored research and $1.85 billion for its endowment in 2013. It also has a long standing rivalry with the Massachusetts Institute of Technology .First year students are required to live on campus, and 95% of undergraduates remain in the on-campus house system. Although Caltech has a strong tradition of practical jokes and pranks, student life is governed by an honor code which allows faculty to assign take-home examinations. The Caltech Beavers compete in 13 intercollegiate sports in the NCAA Division III's Southern California Intercollegiate Athletic Conference. Wikipedia.


Davis M.E.,California Institute of Technology
Chemistry of Materials | Year: 2014

Zeolites and zeolite-like materials are continually finding new applications. Because of the uniformity of these solids, the expression of macroscale materials properties that are controlled by the materials chemistry at the atomic/molecular scale are achievable. In this Perspective, I discuss the following areas of current interest in zeolites and zeolite-like materials that rely on manipulation of the materials chemistry for their preparation and provide new opportunities for application: (i) exploitation of organic structure-directing agents (SDAs) for new materials, (ii) the synthesis of zeolites without SDAs, (iii) the synthesis of very hydrophobic materials, (iv) conversions of two-dimensional (2D) to 3D materials and vice versa, (v) hierarchically organized materials, (vi) chiral materials, and (vii) direction of tetrahedral atoms to specific framework positions. © 2013 American Chemical Society. Source


Rothenberg E.V.,California Institute of Technology
Annual Review of Immunology | Year: 2014

T and B cells share a common somatic gene rearrangement mechanism for assembling the genes that code for their antigen receptors; they also have developmental pathways with many parallels. Shared usage of basic helix-loop-helix E proteins as transcriptional drivers underlies these common features. However, the transcription factor networks in which these E proteins are embedded are different both in membership and in architecture for T and B cell gene regulatory programs. These differences permit lineage commitment decisions to be made in different hierarchical orders. Furthermore, in contrast to B cell gene networks, the T cell gene network architecture for effector differentiation is sufficiently modular so that E protein inputs can be removed. Complete T cell-like effector differentiation can proceed without T cell receptor rearrangement or selection when E proteins are neutralized, yielding natural killer and other innate lymphoid cells. © 2014 by Annual Reviews. All rights reserved. Source


Benson A.J.,California Institute of Technology
Physics Reports | Year: 2010

We review the current theory of how galaxies form within the cosmological framework provided by the cold dark matter paradigm for structure formation. Beginning with the pre-galactic evolution of baryonic material we describe the analytical and numerical understanding of how baryons condense into galaxies, what determines the structure of those galaxies and how internal and external processes (including star formation, merging, active galactic nuclei, etc.) determine their gross properties and evolution. Throughout, we highlight successes and failures of current galaxy formation theory. We include a review of computational implementations of galaxy formation theory and assess their ability to provide reliable modeling of this complex phenomenon. We finish with a discussion of several "hot topics" in contemporary galaxy formation theory and assess future directions for this field. © 2010 Elsevier B.V. Source


Dougherty D.A.,California Institute of Technology
Accounts of Chemical Research | Year: 2013

The chemistry community now recognizes the cation-π interaction as a major force for molecular recognition, joining the hydrophobic effect, the hydrogen bond, and the ion pair in determining macromolecular structure and drug-receptor interactions. This Account provides the author's perspective on the intellectual origins and fundamental nature of the cation-π interaction.Early studies on cyclophanes established that water-soluble, cationic molecules would forego aqueous solvation to enter a hydrophobic cavity if that cavity was lined with π systems. Important gas phase studies established the fundamental nature of the cation-π interaction. The strength of the cation-π interaction (Li+ binds to benzene with 38 kcal/mol of binding energy; NH4 + with 19 kcal/mol) distinguishes it from the weaker polar-π interactions observed in the benzene dimer or water-benzene complexes. In addition to the substantial intrinsic strength of the cation-π interaction in gas phase studies, the cation-π interaction remains energetically significant in aqueous media and under biological conditions. Many studies have shown that cation-π interactions can enhance binding energies by 2-5 kcal/mol, making them competitive with hydrogen bonds and ion pairs in drug-receptor and protein-protein interactions.As with other noncovalent interactions involving aromatic systems, the cation-π interaction includes a substantial electrostatic component. The six (four) C δ--Hδ+ bond dipoles of a molecule like benzene (ethylene) combine to produce a region of negative electrostatic potential on the face of the π system. Simple electrostatics facilitate a natural attraction of cations to the surface. The trend for (gas phase) binding energies is Li+ > Na+ > K+ > Rb+: as the ion gets larger the charge is dispersed over a larger sphere and binding interactions weaken, a classical electrostatic effect. On other hand, polarizability does not define these interactions. Cyclohexane is more polarizable than benzene but a decidedly poorer cation binder.Many studies have documented cation-π interactions in protein structures, where lysine or arginine side chains interact with phenylalanine, tyrosine, or tryptophan. In addition, countless studies have established the importance of the cation-π interaction in a range of biological processes. Our work has focused on molecular neurobiology, and we have shown that neurotransmitters generally use a cation-π interaction to bind to their receptors. We have also shown that many drug-receptor interactions involve cation-π interactions. A cation-π interaction plays a critical role in the binding of nicotine to ACh receptors in the brain, an especially significant case. Other researchers have established important cation-π interactions in the recognition of the "histone code," in terpene biosynthesis, in chemical catalysis, and in many other systems. © 2012 American Chemical Society. Source


Rothenberg E.V.,California Institute of Technology
Trends in Immunology | Year: 2014

T cell development from multipotent progenitors to specialized effector subsets of mature T cells is guided by the iterative action of transcription factors. At each stage, transcription factors interact not only with an existing landscape of histone modifications and nucleosome packing, but also with other bound factors, while they modify the landscape for later-arriving factors in ways that fundamentally affect the control of gene expression. This review covers insights from genome-wide analyses of transcription factor binding and resulting chromatin conformation changes that reveal roles of cytokine signaling in effector T cell programming, the ways in which one factor can completely transform the impacts of previously bound factors, and the ways in which the baseline chromatin landscape is established during early T cell lineage commitment. © 2014 Elsevier Ltd. Source

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