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A Holtzer

Publications and source records attributed to A Holtzer.

52 records · Page 3Linked to original sources

Alpha-helix-to-random-coil transitions of two-chain, coiled coils: a theoretical model for the "pretransition" in cysteine-190-cross-linked tropomyosin.

The thermal unfolding curve for alpha alpha tropomyosin in which the two chains are cross-linked at cysteine-190 shows two striking features that distinguish it from that of its counterpart for non-cross-linked molecules: a "pretransition" at 25-50 degrees C and a shift in the principal transition to higher temperature, but with the same steepness. Previously, the pretransition was explained by postulating that the cross-link produces local strains, yielding a pinched "bubble" of chain-separated random coil about C-190, whereas the rest of the coiled coil remains intact. Results from both enzymatic digestion kinetics and equilibrium calorimetric studies have been interpreted as consistent with the existence of such a bubble. To test this idea further, a theoretical model is devised whereby various physical features can be imposed and the resulting helix content and other properties calculated from the statistical mechanical theory of the helix-coil transition. Short-range interactions employed are the geometric mean values of those in alpha-tropomyosin. The helix-helix interaction free energy is also like that in alpha-tropomyosin, including its nonuniformity; i.e., it is made larger in the amino half of the molecule. Local strain is introduced by setting the helix-helix interaction to zero in a region about the cross-link. The results show that, alone, neither local strain nor nonuniformity serves to mimic the experiments. In concert, however, they reproduce all the main experimental features, if the strain is extensive (approximately 29 residues) and somewhat dissymmetric. Theoretical helix probability profiles, however, show that no bubble of unfolded chains forms about the cross-link. Instead, in the pretransition, residues unfold from the weakly interacting end (residue 284) in to, but not through, the cross-link at C-190. The theory also indicates that the augmented stability for the principal transition occurs largely as a result of loop entropy. The same strain and nonuniformity are then employed to explore the effects of other possible cross-link positions. The thermal curves are shown to depend markedly on cross-link location. The curves are discussed in terms of loop entropy, which has drastic, long-range effects. Under appropriate circumstances it can produce, in the coiled-coil model, a thermal transition that is essentially all or none.

Cysteine↗

Phenomenological analysis of the kinetics of the production of interchain disulfide cross-links in two-chain, coiled-coil proteins by reaction with 5,5'-dithiobis(2-nitrobenzoate).

In parallel, registered, two-chain coiled-coil proteins such as tropomyosin, paramyosin, or myosin rods, a cysteine may appear at the same level on each chain. These may be cross-linked by reaction with 5,5'-dithiobis(2-nitrobenzoate) (NbS2). This technique is useful in several types of studies of such proteins. It is generally accepted that the NbS2, ordinarily at high molar concentration relative to protein, first reacts in a pseudo-first-order process with one cysteine, blocking it by formation of a mixed disulfide (NbS-S-protein); then, the second cysteine either reacts similarly, producing a doubly blocked site, or attacks the mixed disulfide in a sulfhydryl-disulfide interchange to produce an interchain cross-link. Here, the coupled differential equations for such a system are first set up and solved for a molecule with one such cross-linkable site on the assumption that the condition of one sulfhydryl (blocked or unblocked) does not alter the kinetics of its neighbor. Solutions are presented, giving the concentrations of all species as a function of time and of the rate constants for blocking and for cross-linking. It is also shown how nonreducing sodium dodecyl sulfate/polyacrylamide gel electrophoresis experiments on the products allow a determination of the ratio of the two rate constants. The theory is applied to illustrative data on tropomyosin and shown to fit well. Values of both rate constants emerge. A similar analysis is made for the case where two independent cross-linkable sites exist per molecule. The equations are applied to extent data on short subunit 2 of myosin rod.(ABSTRACT TRUNCATED AT 250 WORDS)

Disulfides↗

Alpha-helix to random-coil transition of two-chain, coiled coils: experiments on the thermal denaturation of doubly cross-linked beta beta tropomyosin.

Equilibrium thermal denaturation curves (by circular dichroism) are reported for doubly cross-linked beta beta tropomyosin two-chain coiled coils. Cross-linking was performed by reaction of sulfhydryls with either ferricyanide or 5,5'-dithiobis(2-nitrobenzoate) (NbS2). The extent of reaction was determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and either by titration of residual sulfhydryls with NbS2 (ferricyanide cross-linking) or by determination of mixed disulfide (protein-S-SbN) through reaction with dithiothreitol (NbS2 cross-linking). The results indicate approximately 90% conversion to molecules with interchain cross-links at both C-36 and C-190. Thermal unfolding curves are compared with those obtained previously for non-cross-linked species. The curves are indistinguishable up to approximately 40 degrees C. Above approximately 40 degrees C, the doubly cross-linked species is more stable, but the transition is less steep. This relationship is also compared with that found between alpha alpha tropomyosin (a similar coiled coil made of a genetic variant chain having a sulfhydryl only at C-190) and its singly cross-linked derivative. Thermal curves for alpha alpha and beta beta non-cross-linked species are very similar, alpha alpha being somewhat more stable. For cross-linked alpha alpha, however, the curve sags at temperatures somewhat below the region of principal cooperative loss of helix, the latter occurring at higher temperature but with the same steepness as in the non-cross-linked case. The sag has been ascribed to a "pretransition" in the region of C-190. Thus, doubly and singly cross-linked species differ in that the former show no pretransition and decreased steepness in the principal transition.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Spin-label studies of tropomyosin.

Studies are reported on nitroxide spin-labeled tropomyosin. The labels attach to sulfhydryl groups and to amino groups. The amino spins are highly mobile, the sulfhydryl much less so. Spin count studies show an average of approximately 0.5 labeled sulfhydryl/tropomyosin molecule and only approximately 0.15 labeled amino group/molecule. The spectra are used tostudy the denaturation of tropomyosin by guanidine hydrochloride. The information obtained reveals the course of denaturation at sites near the sulfhydryl group. It is found that these sites are more susceptible to guanidine than the bulk of the molecule; denaturation at the sulfhydryl sites is complete by 1.5 M guanidine, whereas optical studies indicate the molecule as a whole is not completely denatured until the concentration reaches 3.5 M. Spectra are also shown of tropomyosin fibers oriented variously with respect to the applied magnetic field. Strong orientation effects are seen and these indicate that the sulfhydryl-attached spins (but not the amino-attached spins) have a definite orientation in the fiber. Interpretation of the spectra reveals that the normal to the nitroxide plane is inclined to the fiber axis at an angle of 50 degrees. Circular dichroism studies in the tyrosine region also reveal drastic changes with guanidine denaturation, confirming the idea that denaturation produces pronounced increase in mobility at the beta carbon (as in the sulfhydryl casey). A strong negative band existing only in helical tropomyosin at pH's where the tyrosines are uncharged appears to be due to interaction of tyrosines with the helical backbone, whereas the appearance of a strong positive CD band at 250 nm at high pH (approximately11) seems to be ascribable to interaction between the charged phenolic groups and the dissymmetric backbone alpha-carbon atom.

Animals↗

Alpha-helix to random coil transitions of two-chain coiled coils: experiments on the thermal denaturation of beta beta tropomyosin cross-linked selectively at C36.

Current ideas on unfolding equilibria in two-chain, coiled-coil proteins are examined by studies of a species of beta beta tropomyosin that is sulfhydryl blocked at C190 and disulfide cross-linked at C36 (.beta-beta.). The desired species is produced by a seven-step process: (1) Rabbit skeletal muscle, comprising predominantly alpha alpha and alpha beta species, is oxidized with ferricyanide, cross-linking both species at C190. (2) The product is carbamylated at C36 of beta chains, using cyanate in denaturing medium at pH 6. (3) All C190 cross-links are reduced with dithiothreitol (DTT). (4) All C190 sulfhydryls are permanently blocked by carboxyamidomethylation. (5) Chromatography on carboxymethylcellulose in denaturing medium is used to separate C190-blocked alpha chains from C190-blocked, C36-carbamylated beta chains. (6) The latter are decarbamylated in denaturing medium by raising the pH to 8.0. (7) The C190-blocked beta chains are renatured and cross-linked at C36 by ferricyanide. The procedure and the quality of the final product are judged by NaDodSO4/polyacrylamide gel electrophoresis, titration of free sulfhydryls, and electrophoretic analysis of trypsin digestion products. Thermal unfolding curves are reported for the resulting pure .beta-beta. species and for its DTT-reduction product. The latter (.beta beta.) show equilibrium thermal unfolding curves that are very similar to those of the parent beta beta noncross-linked species. The .beta-beta. cross-linked species unfolds in a single-phase, cooperative transition with a melting temperature intermediate between the pretransition and posttransition shown by its cross-linked counterpart, the C190 cross-linked, C36-blocked species (.beta-beta.), which was studied earlier. These transitions are compared with one another and with that of the doubly cross-linked species, beta-(-)beta, in the light of two extant physical models for such transitions. The all-or-none segments model successfully rationalizes the data qualitatively for the .beta-beta. and .beta-beta. species if the usual postulates of greater inherent stability of the amino vs the carboxyl end of the molecule and of strain at each cross-link are accepted. However, the same model then requires that the beta-(-)beta species be the least stable of the three, whereas experiment shows the opposite, thus falsifying the all-or-none segments model. The continuum-of-states model is also qualitatively in accord with data on the .beta-beta. and .beta-beta. species.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗