137 research outputs found
Blogging in the physics classroom: A research-based approach to shaping students' attitudes towards physics
Even though there has been a tremendous amount of research done in how to
help students learn physics, students are still coming away missing a crucial
piece of the puzzle: why bother with physics? Students learn fundamental laws
and how to calculate, but come out of a general physics course without a deep
understanding of how physics has transformed the world around them. In other
words, they get the "how" but not the "why". Studies have shown that students
leave introductory physics courses almost universally with decreased
expectations and with a more negative attitude. This paper will detail an
experiment to address this problem: a course weblog or "blog" which discusses
real-world applications of physics and engages students in discussion and
thinking outside of class. Specifically, students' attitudes towards the value
of physics and its applicability to the real-world were probed using a
26-question Likert scale survey over the course of four semesters in an
introductory physics course at a comprehensive Jesuit university. We found that
students who did not participate in the blog study generally exhibited a
deterioration in attitude towards physics as seen previously. However, students
who read, commented, and were involved with the blog maintained their initially
positive attitudes towards physics. Student response to the blog was
overwhelmingly positive, with students claiming that the blog made the things
we studied in the classroom come alive for them and seem much more relevant.Comment: 20 pages, 6 figure
Small molecule binding sites on the Ras:SOS complex can be exploited for inhibition of Ras activation.
Constitutively active mutant KRas displays a reduced rate of GTP hydrolysis via both intrinsic and GTPase-activating protein-catalyzed mechanisms, resulting in the perpetual activation of Ras pathways. We describe a fragment screening campaign using X-ray crystallography that led to the discovery of three fragment binding sites on the Ras:SOS complex. The identification of tool compounds binding at each of these sites allowed exploration of two new approaches to Ras pathway inhibition by stabilizing or covalently modifying the Ras:SOS complex to prevent the reloading of Ras with GTP. Initially, we identified ligands that bound reversibly to the Ras:SOS complex in two distinct sites, but these compounds were not sufficiently potent inhibitors to validate our stabilization hypothesis. We conclude by demonstrating that covalent modification of Cys118 on Ras leads to a novel mechanism of inhibition of the SOS-mediated interaction between Ras and Raf and is effective at inhibiting the exchange of labeled GDP in both mutant (G12C and G12V) and wild type Ras
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