Abstract:It is demonstrated by theoretical computations that no favorable energy profile for cation transfer can be obtained in a model of the AChR channel constructed with the sole five MI1 helices of the inner wall. A favorable profile is obtained upon including the effect of the remaining helices of the five subunits. The decisive role, for the exit of the ion, of the charged residues situated at the N-terminal of the MI1 segments, established before, is underlined further. The role of the other elements of the chan… Show more
“…We use Madison's coordinates without further optimization for the presence of water or ions in the channel interior, except that we optimize the orientation of the -OH side chain of the five SER 8 residues in two extreme configurations by allowing the H to rotate maximally toward (for anions) or away (for cations) from the channel axis. The present findings supplement those of an earlier modelling of the AChR channel by Furois-Corbin and Pullman [37][38][39] who considered a number of alternative structures.…”
Section: Acetylcholine Receptor Channelsupporting
confidence: 90%
“…Also notice that the energy level in the channel is elevated over that in solution by only about 13 kcal/ M, much less than would occur on taking a Cs + ion out of water into a low dielectric medium. This supports the conclusion of Furois-Corbin and Pullman [36][37][38] that bundles of apolar alpha helices can provide a permeation pathway for ions (also see [56]). It is, however, apparent that the nonspecific interactions with the polyglycine backbone are insufficient to make this structure almost as favorable for cation permeation as it is when lined with polar residues (compare this with the profile for the wildtype channel).…”
Section: Wildsupporting
confidence: 82%
“…Though the helix dipole effect may be less severe in the native channel, where opposing dipoles from other antiparallel alpha helixes are present [38,43], the dipole effects are not likely to be completely neutralized in the channel if M2 lies closest to the channel axis, as is believed [36,37,43]. It should therefore be of considerable interest that differential ionization of the rings of carboxyl and amino residues known to be present at the ends of the channel can produce an almost perfect compensation of such a dipole barrier, as will now be demonstrated.…”
Section: Ionization Of Side Chains Can Compensate the Helix Dipolementioning
“…We use Madison's coordinates without further optimization for the presence of water or ions in the channel interior, except that we optimize the orientation of the -OH side chain of the five SER 8 residues in two extreme configurations by allowing the H to rotate maximally toward (for anions) or away (for cations) from the channel axis. The present findings supplement those of an earlier modelling of the AChR channel by Furois-Corbin and Pullman [37][38][39] who considered a number of alternative structures.…”
Section: Acetylcholine Receptor Channelsupporting
confidence: 90%
“…Also notice that the energy level in the channel is elevated over that in solution by only about 13 kcal/ M, much less than would occur on taking a Cs + ion out of water into a low dielectric medium. This supports the conclusion of Furois-Corbin and Pullman [36][37][38] that bundles of apolar alpha helices can provide a permeation pathway for ions (also see [56]). It is, however, apparent that the nonspecific interactions with the polyglycine backbone are insufficient to make this structure almost as favorable for cation permeation as it is when lined with polar residues (compare this with the profile for the wildtype channel).…”
Section: Wildsupporting
confidence: 82%
“…Though the helix dipole effect may be less severe in the native channel, where opposing dipoles from other antiparallel alpha helixes are present [38,43], the dipole effects are not likely to be completely neutralized in the channel if M2 lies closest to the channel axis, as is believed [36,37,43]. It should therefore be of considerable interest that differential ionization of the rings of carboxyl and amino residues known to be present at the ends of the channel can produce an almost perfect compensation of such a dipole barrier, as will now be demonstrated.…”
Section: Ionization Of Side Chains Can Compensate the Helix Dipolementioning
“…The binding energy of a single ion in the model described in this article is found to be in the order of 50 kcal tool-1 (Figure 7). Similar binding energies are found in other modeling studies [44,45,[69][70][71]. It is known from electrolyte theory that, at equilibrium, charges tend to become neutralized within a Debye length [72].…”
Section: T H E N U M B E R Of Ions In T H E C H a N N E Lsupporting
In this model-building study a model for the pore of the acetylcholine receptor channel is proposed. The pore is formed by five α-helices of the M2 segment where three rings of hydrophilic side chains point into the channel lumen. This model is in agreement with most experimental data like photolabeling, drug affinity studies, single channel conductivity measurements and cryo electron microscopy known about this channel. This study predicts a strong coupling of the motion of the ions in the channel to that of the charged and highly hydrophilic amino acid side chains at the channel wall. Due to the negative net-charge in the pore more than a single cation may occupy the pore region. The resulting strong local electric fields make the commonly used constant field approximation obsolete for this type of ion channel
“…Earlier hypotheses (48,59) fe atured the charged amphipathic MA regions, now thought to be intracellular. (e) Some structural models have also served as the basis for simulations of free energy experienced by probe ions as they move through the channel (44,52,53).…”
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