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J. Biol. Chem., Vol. 280, Issue 8, 6261-6264, February 25, 2005

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The Elasticity of Individual Titin PEVK Exons Measured by Single Molecule Atomic Force Microscopy^*

Atom Sarkar¶||, Sofia Caamano||, and Julio M. Fernandez**

From the Department of Biological Sciences, Columbia University, New York, New York 10027 and the Department of Neurological Surgery, Mayo Clinic College of Medicine, Rochester, Minnesota 55905

Received for publication, December 13, 2004 , and in revised form, January 3, 2005.

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
The I-band region of the giant muscle protein titin contains a large domain enriched for the amino acids proline, glutamate, valine, and lysine and is denoted the PEVK domain. The PEVK domain of titin encodes a random coil shown to be an important factor in the passive elasticity of titin. Muscle-specific splicing of 116 PEVK exons encodes this domain. It has been proposed that proline contents determine the elasticity of the PEVK polypeptide, where the individual exons code for "flexibility cassettes." To test this hypothesis, we have measured the elasticity of three distinct polypeptides encoded by individual PEVK exons (161, 120 and 184) that varied greatly in their proline contents (7, 14, and 37% respectively) and total PEVK contents (55, 70, and 87%). We used single molecule atomic force microscopy techniques to measure the persistence length, p, of the engineered PEVK proteins. Surprisingly, all three exons 161, 120, and 184 coded for proteins with similar values of persistence length, p = 0.92 ± 0.38, 0.89 ± 0.42, and 0.98 ± 0.4 nm, respectively. We conclude that the PEVK exons encode polypeptides of similar elastic properties, unrelated to their total PEVK contents. Hence, alternative splicing solely adjusts the length of the PEVK domain of titin.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
The giant muscle protein titin is crucial to the structural organization in striated muscle sarcomeres (1–3). In addition to the vital role of titin in myofibril architecture by organizing the half-sarcomere, titin is also responsible for the elasticity of myofibrils (4, 5). The elastic region of skeletal muscle titin, corresponding ultrastructurally to the I-band of the sarcomere, is composed of two distinct elastic motifs, tandem repeats of immunoglobulin-like modules (Ig), and random-coiled domains (6–12). While 363 exons encode the entire titin gene, 116 exons encode PEVK¹ domains (2, 13). The expression of PEVK alternative splicing variants has been shown to be a function of factors ranging from tissue specificity, developmental, physiologic, or pathologic cues and leads to myofibrils with distinct passive elasticity (14–17). Prior AFM and electron microscopy single molecule studies showed that a cardiac PEVK isoform behaved as a random coil with structural variations that resulted in persistence length values (p) ranging widely between 0.2 and 2.5 nm (8, 9). Given that the persistence length of a polypeptide chain determines its elasticity, it was surprising that the values of p varied so much between molecules. In this earlier work, it was proposed that proline content, resulting into individualized mixtures of cis and trans conformations, might account for the broad range of persistence lengths observed.

Here we present a study designed to gain a better understanding for the role various exons play in the passive elastic properties of PEVK and whether this is influenced by either proline content alone or rather the overall proline, glutamate, valine, and lysine amino acid content of the PEVK domain. We have used molecular biology techniques to generate three distinct polyprotein chimeras containing PEVK domains encoded by a single exon, fused together with the titin I27 domain. We examined these proteins with single molecule atomic force spectroscopy. The PEVK polyprotein chimera design was essential to unambiguously identify single molecules, a crucial step in correctly measuring the persistence length of the PEVK domains (8, 9, 18). Application of the worm-like chain (WLC) fit to our AFM force-extension curves describes the restoring force as a result of stretching the polymer and is given by,

(Eq. 1)

where F is the force, x is the extension, p is the persistence length, k is the Boltzmann constant, T is the temperature in degrees Kelvin, and L_c is the contour length of the polymer. The parameters of p and L_c are measured by fits to the measured force-extension curves (Fig. 1, A–C, and Fig. 2D, thin lines). In the region where the I27 fingerprint unfolds, consecutive fits measure the increase in contour length associated with each unfolding event (L_c 28 nm), which together with the peak unfolding forces, positively identify a single PEVK containing polyprotein.

View larger version (26K): [in this window] [in a new window]   FIG. 1. Single molecule force spectroscopy identifies and measures the flexibility of the polypeptide encoded by a single PEVK domain. A–C show force-extension traces obtained from single polyproteins engineered to contain repeats of the PEVK polypeptide encoded by exon 120 of the human titin gene; [(exon120PEVK3)I27]4. Below each trace is a schematic representation of the polyprotein. The random coil PEVK domains are shown as green, lavender, or dark blue highlighted curvilinear traces, while I27 is the gold -stranded structure. Those regions not contributing to the force-extension trace are opacified. The force peaks observed in the force-extension traces correspond to I27 domain unfolding, except for the last peak, which corresponds to the detachment of the molecule from the cantilever or the substrate. A WLC fit to the last peak (gold trace) measures the contour length increment after unfolding and extending all its modules. A WLC fit up to 90 pN of the first unfolding peak (lavender trace) measures the contour length and persistence length of the PEVK modules, before any I27 unfolding occurs. A, the trace shows an initial extension to a contour length of Lc = 72.5 nm followed by the unfolding of three I27 modules. In the initial extension, the three folded I27 modules contribute to the initial contour length by 4.5 nm/folded I27 domain. Subtracting this contribution we calculate a PEVK contour length of 59 nm (see text). This extension is consistent with the elongation of two PEVK domains. B, the trace shows an initial extension corresponding to three PEVK domains (93 nm), followed by the unfolding of four I27 domains. C, while only three I27s unfold in this trace (similar to A), the initial extension corresponds to four PEVK domains (119 nm). D, histogram of I27 peak unfolding forces from all polyprotein recordings used in this study. The mean I27 unfolding force was 196 ± 30 pN, bin width = 10 pN, n = 823, collected from 239 force-extension traces.

View larger version (27K): [in this window] [in a new window]   FIG. 2. Similar persistence length values found in polypeptides from different PEVK exons. A–C, histograms of the persistence length values, p, measured from polyproteins engineered with PEVK modules from different exons. Fits of the WLC model of polymer elasticity to the PEVK domain force-extension relationships, measured the persistence length, p (see text and Fig. 1). A, histogram of persistence length values (average p = 0.89 nm, range = 0.35–2 nm), from 60 recordings from polyproteins containing PEVK exon 120, [(exon120PEVK)3I27]4. B, histogram of ninety-four persistence length values (average p = 0.92 nm, range = 0.29–1.87 nm) from polyprotein recordings containing PEVK exon 161, [(exon161PEVK)3 I27]4. C, histogram of persistence length values (average p = 0.98 nm, range = 0.26–2 nm), from 85 recordings of polyproteins containing PEVK exon 184, [(exon184PEVK)3I27]4. D, two representative force versus extension traces obtained from the [(exon120PEVK)3 I27]4 polyprotein are shown in black and green. Both curves show the initial extension of four PEVK domains (120 nm) followed by four I27 unfolding events. Although the two molecules are of similar total contour length, the PEVK extension shows very different persistence lengths (0.38 nm versus 1.93 nm). The boxed gray region is shown in greater detail at the top of the panel. The superposition of the two force-extension curves shows graphically the large variations in flexibility of molecules originating from the same PEVK exon.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Construction of the [(PEVK)₃I27]₄ Polyproteins—The method for protein engineering, utilizing successive cycles of BamHI/BglII sticky end ligations, has been described previously (20, 21). Polyprotein constructs used in this study were based on the human titin I27 and PEVK sequence (4, 14). While the human titin gene contains 116 exons coding for PEVK sequences, we have confined our investigation to exons 120, 161, and 184. All three exons are approximately equal in size (encoding 27, 28, or 30 amino acids, respectively) but contrast in proline as well as overall PEVK content. Specifically exon 120 contains 4 prolines with an overall PEVK content equal to 70%, exon 161 has 2 prolines with an overall PEVK of 55%, and exon 184 has 11 prolines with 87% of its content made up by PEVK amino acids. Thus these three selected exons provide a range of proline and PEVK composition, features that make them ideal to use in an examination of the exon-specific contribution to PEVK flexibility. The core sequence for our polyprotein chimeras was always three identical tandem repeats of a PEVK exon (which we refer to as a single PEVK domain), followed by an I27 module, with the core sequence repeated four times. The finished constructs had the following structure: [(^exon120PEVK)₃I27]₄, [(^exon161PEVK)₃I27]_4, or [(^exon184PEVK)₃I27]₄. Additionally all constructs contained two terminal cysteine-cysteine residues to orient a covalent protein attachment to the gold substrate during AFM experiments (20). Polyprotein expression in bacteria, as well as protein purification by Ni²⁺ chelation and size exclusion chromatography, have also been described previously (20).

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
The polyproteins used in this study were constructed from single PEVK exons and an I27 domain. Because the number of amino acids in the selected PEVK exons is approximately one-third the number of amino acids in the I27 domain (27–30 versus 89 amino acids, respectively), all the chimeric polyproteins were designed to include three repeats of a single PEVK exon linked to I27 as the core sequence, which was repeated 4-fold such that any of our recombinant constructs always contained 12 identical copies of a PEVK exon and four I27 domains. This can be appreciated in the cartoons of Fig. 1, A–C, where three identical PEVK exons are placed in tandem and represented by the green, lavender, and dark blue coiled structures, followed by the -stranded I27 domain shown in gold, and repeated four times. By engineering such a polyprotein, we were able to confine our analysis to only those AFM force-extension traces in which the well described signature of I27 unfolding was present, namely a contour length increase of 28 nm, as well as a peak unfolding force of 200 pN (21, 22). Our method of analysis is highlighted in Fig. 1. Panel A in Fig. 1 illustrates a typical force-extension sawtooth pattern trace. In this experiment three I27 unfolding peaks are present, while the last peak represents the detachment of the protein from either the cantilever or the surface. The initial featureless region of the force-extension curve corresponds to the extension of the PEVK domain. We fit this region with the WLC model up to 90 pN, just before the first unfolding peak of the I27 fingerprint (Equation 1; Fig. 1, A–C, thin lavender trace). Following the extension of the PEVK domain, we fit the WLC to the unfolding peaks to identify the I27 fingerprint. We explicitly measure L_c per I27 unfolding event by measuring the difference in the contour length between the first and the last unfolding peaks and dividing by the total number of events (20). In Fig. 1A we measured L_c = 86.4 nm, which divided by three events, gives L_c = 28.2 nm per unfolding. This value together with unfolding forces of 200 pN defines the mechanical unfolding of three I27 modules (8, 9, 20, 21). Given that we pick up molecules from random locations, the number of I27 peaks that we observe varies from molecule to molecule. In this study, we have only included recordings showing at least two I27 unfolding events. The three I27 unfolding peaks shown in Fig. 1A indicate that there must be at least two and at most four PEVK domains being stretched in the initial force-extension trace for this molecule (8, 21).

A single PEVK exon, repeated three times, represents a PEVK domain within our polyprotein of either 81 (exon 120), 84 (exon 161), or 90 (exon 184) amino acids. Since each amino acid contributes 0.38 nm/residue (23), this will result in the extension of each PEVK domain to a contour length of L_c = 30.8, 31.9, or 34.2 nm for exons 120, 161, or 184, respectively. Due to the characteristic lack of mechanical resistance of a random coil, the extension of a PEVK domain will always occur before any I27 unfolding event. A WLC fit to the initial extension observed in the AFM recording from a [(^exon120PEVK)₃I27]₄ polyprotein shown in Fig. 1A measures L_c = 72.5 nm. While the extension of this region is predominantly from the PEVK domain, part of this extension represents a contribution from the three folded I27 modules, 4.5 nm/folded I27 domain (22, 24), and has to be subtracted from the measured L_c. A corrected L_c value of 59 nm is consistent with the extension of two PEVK domains (two exon 120 domains, see above; L_c = 61.6 nm). Hence, in the schematic below the trace in Fig. 1A, the first two PEVK domains, as well as the first I27 domain are opacified given that they do not contribute to the force extension curve. Fig. 1B illustrates four I27 unfolding events preceded by an initial PEVK extension of 93 nm, corresponding to three PEVK domains, while the three I27 unfoldings of Fig. 1C are preceded by an initial PEVK extension of 119 nm corresponding to the extension of all four PEVK domains. Fig. 1D shows a histogram of the peak unfolding force for the I27 fingerprint from all 239 recordings used in our study The mean value of the unfolding force was 196 ± 30 pN (n = 823), which was similar to our prior results (20, 21).

All single molecule traces used in our analysis had to meet the strict criteria outlined above, namely that a regular saw-tooth pattern of I27 unfolding events had to be preceded by a PEVK extension corresponding to integer multiples of a PEVK domain. WLC fits to the PEVK domain (thin lavender lines in Fig. 1, A–C) are done before any I27 module unfolds. The persistence length of a folded I27 polyprotein is large and was measured to be p = 9.8 nm (see supplementary information in Ref. 9), marking a rigid protein. Furthermore, an individual I27 module is likely to be much stiffer than the I27 polyprotein. Hence, it is reasonable to assume that in the case of the PEVK-I27 polyproteins studied here, I27 modules, prior to their unfolding, do not contribute to the flexibility of the PEVK domains being measured.

We were able to collect 60, 94, and 85 single molecule recordings for the PEVK exons 120, 161, and 184, respectively. WLC fits to the initial extension of the [(^exon120PEVK)₃I27]₄ polyprotein (sixty recordings) measured the persistence length shown in the histogram of Fig. 2A. The bin widths are set to 0.15 nm (8), and the mean value of the measured persistence length for this exon is p = 0.89 ± 0.42 nm. The same wide distribution of persistence length values was observed for the other two PEVK exons. WLC fits to the initial extension of the [(^exon161PEVK)₃I27]₄ polyprotein (94 recordings) gave an average persistence length of p = 0.92 ± 0.38 nm (Fig. 2B), whereas the fits to the [(^exon184PEVK)₃I27]₄ polyprotein (85 recordings) gave an average persistence length of p = 0.98 ± 0.4 nm (Fig. 2C). Fig. 2D shows two recordings obtained from [(^exon120PEVK)₃I27]₄ polyproteins, which are similar in length and have the same number of I27 unfolding events (four), yet their PEVK domains show very different values of persistence length (p = 0.38 nm versus p = 1.93 nm). These recordings highlight the variations in the persistence length of the PEVK domains.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Of the 363 exons encoding titin, the elastic I-band region is encoded by a total of 251 exons, highlighting the importance of alternative splicing in controlling titin elasticity (2). The I-band comprises of 135 exons coding for immunoglobulin domains and unique sequences and there are 116 exons coding for PEVK sequences (2). It is believed that each of the approximately 600 striated muscles of the human body will have a unique alternatively spliced form of titin (4). For example, cardiac titin possesses two extensible regions of unknown structure, the N2B unique region and the PEVK region. The unique cardiac-specific N2B and PEVK regions are 572 and 186 amino acids long, respectively. The mechanical properties of these regions were recently examined by single molecule AFM techniques and were found to behave like extensible random coils (7–9). In contrast to mechanically stable folded proteins like the immunoglobulin domains of titin (20), an unstructured protein domain generates a recoiling force that changes monotonically with its length (8). This recoiling force is well described by simple models of polymer elasticity, where the flexibility of the chain is defined by the persistence length, p. For unstructured proteins of equal length a higher value of p predicts a lower force at any given extension. Hence we were surprised to find that the persistence length of the cardiac specific PEVK varied widely from molecule to molecule between values of p = 0.3–2.3 nm (8), in sharp contrast with the persistence length of the N2B unique region, which was narrowly distributed around a mean value of p = 0.66 nm (8, 9). The wide variations in the persistence length of the cardiac PEVK were attributed to result from the different conformations of its proline residues. Such conformations were thought to be the result of polyproline type I (cis) and type II (trans) helical structures (8), and the two allowed conformations of the trans prolyl residues (25). Extrapolating from these results, we proposed that the proline content encoded into each of the 116 PEVK exons would result into modular flexibility cassettes that through alternative splicing, tune the elasticity of a given myofibril.

In a more recent study, Granzier and colleagues used protein engineering and single molecule AFM techniques to measure the persistence length of multi-exon PEVK constructs (18). They showed a histogram of the measured persistence length for a PEVK protein encompassing exons 119 to 136. These combined PEVK exons showed a wide persistence length distribution, p = 0.3–2.7 nm, which was very similar to the cardiac specific PEVK. Hence, these experiments did not resolve the question of whether individual exons code for protein sequences with well defined and narrowly distributed persistence length values.

The experiments that we report here were designed to test the "flexibility cassette" hypothesis. We engineered polyproteins that contained multiple repeats of a single PEVK exon, combined with an unfolding fingerprint used to identify single molecules (8, 9, 18). For our study, we chose the PEVK exons 161, 120, and 184, which contained 7, 14, and 37% proline, respectively. This range covered the proline content found in the cardiac titin N2B unique (7%) and cardiac PEVK (23%) sequences. In contrast to our expectations, we found that in all three cases the persistence length values were distributed broadly, p = 0.26–2 nm, similar to all prior multi-exon single molecule measurements of PEVK protein flexibility (8, 9, 18). Given that there are still 113 exons to be examined at the single exon level with single molecule techniques, we cannot rule out the existence of persistence length distributions that are exon-specific. However, our current data does not support the flexibility cassette hypothesis for PEVK exons. Alternatively, the diversity of PEVK exons may simply represent a strategy for the fine length adjustment of a random coil-like protein, without ever repeating the same sequence. In this scenario, all PEVK proteins would show the same range of persistence length values, in agreement with the current literature and our latest observations (Fig. 3).

View larger version (20K): [in this window] [in a new window]   FIG. 3. A composite picture of PEVK persistence length variation. The measured persistence length values from all three [(PEVK)3I27]4 constructs were pooled and shown in gray (average p = 0.93 nm, range = 0.26–2 nm, n = 239). For comparison, our earlier work investigating the persistence length of the cardiac specific, multi-exon PEVK isoform (8) (n = 118, range = 0.3–2.5 nm) is overlaid (magenta trace) onto our current data. As shown, all PEVK constructs show similar values of persistence length.

	FOOTNOTES

 
^* This work was supported in part by funding from the National Institutes of Health (to J. M. F.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

^¶ Supported in part by a fellowship from the Neurosurgery Research and Education Foundation.

^|| These two authors contributed equally to this work.

^** To whom correspondences should be addressed: Dept. of Biological Sciences, Columbia University, 1011A Fairchild Center, 1212 Amsterdam Ave., MC 2449, New York, NY 10027. Tel.: 212-854-2090; Fax: 212-854-4619; E-mail: jfernandez{at}columbia.edu.

¹ The abbreviations used are: PEVK, proline, glutamate, valine, and lysine; AFM, atomic force microscope; I27, 27th immunoglobulin module from human titin; WLC, worm-like chain.

	ACKNOWLEDGMENTS

 
We thank Drs. H. Li and A. S. R. Koti and R. B. Robertson for their help.

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TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 

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