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This invention relates to a process for producing a semiconductor film, and, more particularly, to a process for producing a semiconductor film used for a semiconductor device such as a thin film transistor.
2. Description of the Related Art
Processes for the production of a semiconductor are generally classified into two systems: (1) a vapor-phase growth process of crystallizing or growing a semiconductor film directly on a substrate using a heat reaction or a catalytic reaction and (2) a vapor-phase growth process of forming a semiconductor film on a substrate with a catalytic reaction by decomposing a raw gas in an atmosphere of a heated catalytic gas.
In the former process, the substrate is directly subjected to the heat reaction or the catalytic reaction. Thus, a semiconductor film formed on a substrate is usually inferior in crystallinity, and a reaction is needed to enhance the crystallinity. Further, when an amorphous silicon semiconductor film is subjected to heat treatment at 400-600.degree. C. to be crystallized, it is known that a crystalline silicon (polycrystalline silicon) film is formed.
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The seventh season of MTV’s scripted series “Jersey Shore”, is now available on Hulu for new subscribers, and for Hulu Plus subscribers. and the nuclear import of protein through the transportin2 system.** The transportin2 complex binds to the signal sequence of the amino-acids cotransported with the preproteins through their nuclear localization sequences (Kaneko, [@B26]).
*Premature termination of proteasome-mediated degradation. Proteasomes bind to the signal sequence of the preproteins and destroy them, and to ensure their destruction, the signals need to be removed. Proteasome-mediated degradation is completed when signal peptide in the preprotein is released to the inner surface of the membrane. The preproteins are also likely translocated through the 5-nm channels formed by the oligomeric rings of the proteasome caps in yeast* (Tanaka et al., [@B56]; Figure [4](#F4){ref-type=”fig”}) *and in human cells* (Uemura et al., [@B57]).
Concluding remarks
==================
Protein targeting is a crucial process in living cells. Although a number of targeting factors have been identified, including proteinaceous motor driven systems and diffusion-driven systems (see the review by Minta and Warren, [@B43] for details), targeting of preproteins is still a rather unexplored area. Our newly designed, fundamentally new approach allows the detailed investigation of the question of how the preproteins are targeted (see Figure [4](#F4){ref-type=”fig”}) in living cells.
![**Schematic illustration of the targeting mechanism of preproteins in living cells.** The preproteins are efficiently transported through the nuclear envelope. The preproteins are targeted to the ER membrane and are efficiently transported through the nuclear pores. Moreover, the preproteins are also targeted to the plasma membrane, the mitochondria, and the nucleus.](fphys-03-00137-g004){#F4}
1. How are preproteins targeted to
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