Literature DB >> 19723816

Using affinity chromatography to investigate novel protein-protein interactions in an undergraduate cell and molecular biology lab course.

Kenneth D Belanger1.   

Abstract

Inquiry-driven lab exercises require students to think carefully about a question, carry out an investigation of that question, and critically analyze the results of their investigation. Here, we describe the implementation and assessment of an inquiry-based laboratory exercise in which students obtain and analyze novel data that contribute to our understanding of macromolecular trafficking between the nucleus and cytoplasm in eukaryotic cells. Although many of the proteins involved in nucleocytoplasmic transport are known, the physical interactions between some of these polypeptides remain uncharacterized. In this cell and molecular biology lab exercise, students investigate novel protein-protein interactions between factors involved in nuclear RNA export. Using recombinant protein expression, protein extraction, affinity chromatography, SDS-polyacrylamide gel electrophoresis, and Western blotting, undergraduates in a sophomore-level lab course identified a previously unreported association between the soluble mRNA transport factor Mex67 and the C-terminal region of the yeast nuclear pore complex protein Nup1. This exercise immersed students in the process of investigative science, from proposing and performing experiments through analyzing data and reporting outcomes. On completion of this investigative lab sequence, students reported enhanced understanding of the scientific process, increased proficiency with cellular and molecular methods and content, greater understanding of data analysis and the importance of appropriate controls, an enhanced ability to communicate science effectively, and an increased enthusiasm for scientific research and for the lab component of the course. The modular nature of this exercise and its focus on asking novel questions about protein-protein interactions make it easily transferable to undergraduate lab courses performed in a wide variety of contexts.

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Year:  2009        PMID: 19723816      PMCID: PMC2736025          DOI: 10.1187/cbe.09-03-0019

Source DB:  PubMed          Journal:  CBE Life Sci Educ        ISSN: 1931-7913            Impact factor:   3.325


  22 in total

1.  Using the two-hybrid screen in the classroom laboratory.

Authors:  Daniel P Odom; Martha J Grossel
Journal:  Cell Biol Educ       Date:  2002

2.  The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores.

Authors:  Tamás Fischer; Katja Strässer; Attila Rácz; Susana Rodriguez-Navarro; Marisa Oppizzi; Petra Ihrig; Johannes Lechner; Ed Hurt
Journal:  EMBO J       Date:  2002-11-01       Impact factor: 11.598

3.  The NUP1 gene encodes an essential component of the yeast nuclear pore complex.

Authors:  L I Davis; G R Fink
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

4.  The GLFG regions of Nup116p and Nup100p serve as binding sites for both Kap95p and Mex67p at the nuclear pore complex.

Authors:  L A Strawn; T Shen; S R Wente
Journal:  J Biol Chem       Date:  2000-12-04       Impact factor: 5.157

5.  The yeast nucleoporin Nup2p is involved in nuclear export of importin alpha/Srp1p.

Authors:  J W Booth; K D Belanger; M I Sannella; L I Davis
Journal:  J Biol Chem       Date:  1999-11-05       Impact factor: 5.157

6.  Characterization of pathogenic human MSH2 missense mutations using yeast as a model system: a laboratory course in molecular biology.

Authors:  Alison E Gammie; Naz Erdeniz
Journal:  Cell Biol Educ       Date:  2004

7.  Analysis of protein localization and secretory pathway function using the yeast Saccharomyces cerevisiae.

Authors:  Elizabeth Vallen
Journal:  Cell Biol Educ       Date:  2002

8.  Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method.

Authors:  R Daniel Gietz; Robin A Woods
Journal:  Methods Enzymol       Date:  2002       Impact factor: 1.600

9.  Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export.

Authors:  K Strässer; J Bassler; E Hurt
Journal:  J Cell Biol       Date:  2000-08-21       Impact factor: 10.539

10.  Proteomic analysis of the mammalian nuclear pore complex.

Authors:  Janet M Cronshaw; Andrew N Krutchinsky; Wenzhu Zhang; Brian T Chait; Michael J Matunis
Journal:  J Cell Biol       Date:  2002-08-26       Impact factor: 10.539

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  2 in total

Review 1.  The development and characterization of protein-based stationary phases for studying drug-protein and protein-protein interactions.

Authors:  Mitesh Sanghvi; Ruin Moaddel; Irving W Wainer
Journal:  J Chromatogr A       Date:  2011-05-27       Impact factor: 4.759

2.  Promoting inquiry-based teaching in laboratory courses: are we meeting the grade?

Authors:  Christopher Beck; Amy Butler; Karen Burke da Silva
Journal:  CBE Life Sci Educ       Date:  2014       Impact factor: 3.325

  2 in total

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