Colicin Ia, a 626-residue bactericidal protein, consists of three domains, with the carboxy-terminal domain (C domain) responsible for channel formation. Whole colicin Ia or C domain added to a planar lipid bilayer membrane forms voltage-gated channels. We have shown previously that the channel formed by whole colicin Ia has four membrane-spanning segments and an ∼68-residue segment translocated across the membrane. Various experimental interventions could cause a longer or shorter segment within the C domain to be translocated, making us wonder why translocation normally stops where it does, near the amino-terminal end of the C domain (approximately residue 450). We hypothesized that regions upstream from the C domain prevent its amino-terminal end from moving into and across the membrane. To test this idea, we prepared C domain with a ligand attached near its amino terminus, added it to one side of a planar bilayer to form channels, and then probed from the opposite side with a water-soluble protein that can specifically bind the ligand. The binding of the probe had a dramatic effect on channel gating, demonstrating that the ligand (and hence the amino-terminal end of the C domain) had moved across the membrane. Experiments with larger colicin Ia fragments showed that a region of more than 165 residues, upstream from the C domain, can also move across the membrane. All of the colicin Ia carboxy-terminal fragments that we examined form channels that pass from a state of relatively normal conductance to a low-conductance state; we interpret this passage as a transition from a channel with four membrane-spanning segments to one with only three.
Protein Translocation across Planar Bilayers by the Colicin Ia Channel-Forming Domain: Where Will It End?
Portions of this work were previously published in abstract form (Kienker, P., S. Slatin, K. Jakes, and A. Finkelstein. 1999. Biophys. J. 76:A120).
Abbreviations used in this paper: CT-L, colicin Ia carboxy-terminal fragment 327–626; CT-M, CT fragment 438–626; CT-S, CT fragment 453–626; CT-XL, CT fragment 282–626; DTT, dithiothreitol.
The nature of the reverse-gating channel is of interest in its own right, but it is not essential to the present study; we plan to examine this topic in greater detail in a subsequent communication.
This “normal” channel behavior was observed for streptavidin-preincubated C domain from which the amino-terminal His-tag had been removed. If the His-tag was left on, the channels flickered to a nonconducting “blocked” state in a voltage-dependent manner. This interesting phenomenon will be considered in a subsequent paper.
How much of the long helix 1 “belongs” to the C domain is somewhat arbitrary. Trypsin digestion of colicin Ia results in a channel-forming carboxy-terminal fragment that begins at residue 451 (Ghosh et al. 1993), which is conventionally taken as the amino terminus of the C domain.
Paul K. Kienker, Karen S. Jakes, Alan Finkelstein; Protein Translocation across Planar Bilayers by the Colicin Ia Channel-Forming Domain: Where Will It End?. J Gen Physiol 1 October 2000; 116 (4): 587–598. doi: https://doi.org/10.1085/jgp.116.4.587
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