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Real-time trafficking and assembly of ribosomal subunits

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Title: Real-time trafficking and assembly of ribosomal subunits
Author: Wang, Jason
Abstract: Nuclear pore complexes (NPCs) facilitate the bidirectional transport of a myriad of molecules, ranging in size from an ion to assembled ribosomal subunits, across the two lipid bilayers that constitute the nuclear envelope (NE). Research over the past decade has imparted much insight into how NPCs control the selective passage of large macromolecules while maintaining their compartmentalization properties. Schemes for soluble cofactor-mediated active transport have been developed through phenotypic mutational analyses and in vitro experiments. Continuing the effort for a more comprehensive characterization of NPC function, we have developed a method for the in vivo analysis of nucleocytoplasmic transport utilizing fluorescently labeled, recombinant human ribosomal protein L23a (rpL23a-His). Cytoplasmic microinjections into live HeLa cells indicated rapid nuclear import and subsequent export of rpL23a-His. These results are expected to lead to real-time in vivo single-molecule observation of ribosomal subunit trafficking and assembly.
Description: Due to the character of the original source materials and the nature of batch digitization, quality control issues may be present in this document. Please report any quality issues you encounter to digital@library.tamu.edu, referencing the URI of the item.
Includes bibliographical references (leaves 26-27).
Publisher: Texas A&M University
Majors genetics and biochemistry.
URI: http://hdl.handle.net/1969.1/ETD-TAMU-2004-Fellows-Thesis-W26
Date: 2004


Wang, Jason (2004). Real-time trafficking and assembly of ribosomal subunits. Texas A&M University. Available electronically from http : / /hdl .handle .net /1969 .1 /ETD -TAMU -2004 -Fellows -Thesis -W26.

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