Titin

Titin[5] /ˈtaɪtɪn/ (contraction for Titan protein) (also called connectin) is a protein that in humans is encoded by the TTN gene.[6][7] Titin is a giant protein, greater than 1 µm in length,[8] that functions as a molecular spring that is responsible for the passive elasticity of muscle. It comprises 244 individually folded protein domains connected by unstructured peptide sequences.[9] These domains unfold when the protein is stretched and refold when the tension is removed.[10]

Not to be confused with Titan, Tintin, or Titian.
TTN
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTTN, CMD1G, CMH9, CMPD4, EOMFC, HMERF, LGMD2J, MYLK5, TMD, titin, SALMY, LGMDR10
External IDsOMIM: 188840 MGI: 98864 HomoloGene: 130650 GeneCards: TTN
EC number2.7.11.1
Orthologs
SpeciesHumanMouse
Entrez

7273

22138

Ensembl

ENSG00000155657

ENSMUSG00000051747

UniProt

Q8WZ42

A2ASS6

RefSeq (mRNA)

NM_011652
NM_028004

RefSeq (protein)

NP_035782
NP_082280
NP_001372637

Location (UCSC)Chr 2: 178.53 – 178.83 MbChr 2: 76.7 – 76.98 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Cardiac sarcomere structure, featuring titin

Titin is important in the contraction of striated muscle tissues. It connects the Z disc to the M line in the sarcomere. The protein contributes to force transmission at the Z disc and resting tension in the I band region.[11] It limits the range of motion of the sarcomere in tension, thus contributing to the passive stiffness of muscle. Variations in the sequence of titin between different types of striated muscle (cardiac or skeletal) have been correlated with differences in the mechanical properties of these muscles.[6][12]

Titin is the third most abundant protein in muscle (after myosin and actin), and an adult human contains approximately 0.5 kg of titin.[13] With its length of ~27,000 to ~35,000 amino acids (depending on the splice isoform), titin is the largest known protein.[14] Furthermore, the gene for titin contains the largest number of exons (363) discovered in any single gene,[15] as well as the longest single exon (17,106 bp).

Discovery

In 1954, Reiji Natori proposed the existence of an elastic structure in muscle fiber to account for the return to the resting state when muscles are stretched and then released.[16] In 1977, Koscak Maruyama and coworkers isolated an elastic protein from muscle fiber that they called connectin.[17] Two years later, Kuan Wang and coworkers identified a doublet band on electrophoresis gel corresponding to a high molecular weight, elastic protein that they named titin.[5][18]

In 1990, Siegfried Labeit isolated a partial cDNA clone of titin.[7] Five years later, Labeit and Bernhard Kolmerer determined the cDNA sequence of human cardiac titin.[9] In 2001, Labeit and colleagues determined the complete sequence of the human titin gene.[15][19]

Genetics

The human gene encoding for titin is located on the long arm of chromosome 2 and contains 363 exons, which together code for 38,138 amino acid residues (4200 kDa).[15] Within the gene are found a large number of PEVK (proline-glutamate-valine-lysine -abundant structural motifs) exons 84 to 99 nucleotides in length, which code for conserved 28- to 33-residue motifs that may represent structural units of the titin PEVK spring. The number of PEVK motifs in the titin gene appears to have increased during evolution, apparently modifying the genomic region responsible for titin's spring properties.[20]

Isoforms

A number of titin isoforms are produced in different striated muscle tissues as a result of alternative splicing.[21] All but one of these isoforms are in the range of ~27,000 to ~36,000 amino acid residues in length. The exception is the small cardiac novex-3 isoform, which is only 5,604 amino acid residues in length. The following table lists the known titin isoforms:

IsoformAlias/descriptionLengthMolecular weight
Q8WZ42-1The "canonical" sequence34,3503,816,030
Q8WZ42-234,2583,805,708
Q8WZ42-3Small cardiac N2-B26,9262,992,939
Q8WZ42-4Soleus33,4453,716,027
Q8WZ42-532,9003,653,085
Q8WZ42-6Small cardiac novex-35,604631,567
Q8WZ42-7Cardiac novex-233,6153,734,648
Q8WZ42-8Cardiac novex-134,4753,829,846
Q8WZ42-927,1183,013,957
Q8WZ42-1027,0513,006,755
Q8WZ42-1133,4233,713,600
Q8WZ42-1235,9913,994,625
Q8WZ42-1334,4843,831,069

Structure

Titin is the largest known protein; its human variant consists of 34,350 amino acids, with the molecular weight of the mature "canonical" isoform of the protein being approximately 3,816,030.05 Da.[22] Its mouse homologue is even larger, comprising 35,213 amino acids with a molecular weight of 3,906,487.6 Da.[23] It has a theoretical isoelectric point of 6.02.[22] The protein's empirical chemical formula is C169,719H270,466N45,688O52,238S911.[22] It has a theoretical instability index (II) of 42.38, classifying the protein as unstable.[22] The protein's in vivo half-life, the time it takes for half of the amount of protein in a cell to break down after its synthesis in the cell, is predicted to be approximately 30 hours (in mammalian reticulocytes).[21]

Titin Ig domains. a) Schematic of part of a sarcomere b) Structure of Ig domains c) Topology of Ig domains.[24]

The Titin protein is located between the myosin thick filament and the Z disk.[25] Titin consists primarily of a linear array of two types of modules, also referred to as protein domains (244 copies in total): type I fibronectin type III domain (132 copies) and type II immunoglobulin domain (112 copies).[13][9] However, the exact number of these domains is different in different species. This linear array is further organized into two regions:

  • N-terminal I-band: acts as the elastic part of the molecule and is composed mainly of type II modules. More specifically the I-band contains two regions of tandem type II immunoglobulin domains on either side of a PEVK region that is rich in proline (P), glutamate (E), valine (V) and lysine (K).[25]
  • C-terminal A-band: is thought to act as a protein-ruler and is composed of alternating type I (Fn3) and II (Ig) modules with super-repeat segments. These have been shown to align to the 43 nm axial repeats of myosin thick filaments with immunoglobulin domains correlating to myosin crowns.[26]

The C-terminal region also contains a serine kinase domain[27][28] that is primarily known for adapting the muscle to mechanical strain.[29] It is “stretch-sensitive” and helps repair overstretching of the sarcomere.[30] The N-terminal (the Z-disc end) contains a "Z repeat" that recognizes Actinin alpha 2.[31]

Protein domains of Titin A-band. White boxes are Fn3 domains, red boxes are Ig domains, yellow boxes are Fn3 domains with the -AVNKYG- sequence, and the black box is protein kinase domain.[32]

The elasticity of the PEVK region has both entropic and enthalpic contributions and is characterized by a polymer persistence length and a stretch modulus.[33] At low to moderate extensions PEVK elasticity can be modeled with a standard worm-like chain (WLC) model of entropic elasticity. At high extensions PEVK stretching can be modeled with a modified WLC model that incorporates enthalpic elasticity. The difference between low-and high- stretch elasticity is due to electrostatic stiffening and hydrophobic effects.

Embedded between the PEVK and Ig residues are N2A domains.[34]

Evolution

The titin domains have evolved from a common ancestor through many gene duplication events.[35] Domain duplication was facilitated by the fact that most domains are encoded by single exons. Other giant sarcomeric proteins made out of Fn3/Ig repeats include obscurin and myomesin. Throughout evolution, titin mechanical strength appears to decrease through the loss of disulfide bonds as the organism becomes heavier.[36]

Titin A-band has homologs in invertebrates, such as twitchin (unc-22) and projectin, which also contain Ig and FNIII repeats and a protein kinase domain.[30] The gene duplication events took place independently but were from the same ancestral Ig and FNIII domains. It is said that the protein titin was the first to diverge out of the family.[28] Drosophila projectin, officially known as bent (bt), is associated with lethality by failing to escape the eggnog in some mutations as well as dominant changes in wing angles.[37][38][39]

Titin repeat
Identifiers
SymbolTitin_Ig-rpts
PfamPF06582
InterProIPR010939
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Drosophila Titin, also known as Kettin or sallimus (sls), is kinase-free. It has roles in the elasticity of both muscle and chromosomes. It is homologous to vertebrate titin I-band and contains Ig PEVK domains, the many repeats being a hot target for splicing.[40] There also exists a titin homologue, ttn-1, in C. elegans.[41] It has a kinase domain, some Ig/Fn3 repeats, and PEVT repeats that are similarly elastic.[42]

Function
Sliding filament model of muscle contraction. (Titin labeled at upper right.)

Titin is a large abundant protein of striated muscle. Titin's primary functions are to stabilize the thick filament, center it between the thin filaments, prevent overstretching of the sarcomere, and to recoil the sarcomere like a spring after it is stretched.[43] An N-terminal Z-disc region and a C-terminal M-line region bind to the Z-line and M-line of the sarcomere, respectively, so that a single titin molecule spans half the length of a sarcomere. Titin also contains binding sites for muscle-associated proteins so it serves as an adhesion template for the assembly of contractile machinery in muscle cells. It has also been identified as a structural protein for chromosomes.[44][45] Considerable variability exists in the I-band, the M-line and the Z-disc regions of titin. Variability in the I-band region contributes to the differences in elasticity of different titin isoforms and, therefore, to the differences in elasticity of different muscle types. Of the many titin variants identified, five are described with complete transcript information available.[6][7]

Dominant mutation in TTN causes predisposition to hernias.[46]

Titin interacts with many sarcomeric proteins including:[15]

Clinical relevance

Mutations anywhere within the unusually long sequence of this gene can cause premature stop codons or other defects. Titin mutations are associated with hereditary myopathy with early respiratory failure,[47][48] early-onset myopathy with fatal cardiomyopathy,[49] core myopathy with heart disease, centronuclear myopathy, limb-girdle muscular dystrophy type 2J,[50] familial dilated cardiomyopathy 9,[11][51] hypertrophic cardiomyopathy and tibial muscular dystrophy.[52] Further research also suggests that no genetically linked form of any dystrophy or myopathy can be safely excluded from being caused by a mutation on the TTN gene.[50] Truncating mutations in dilated cardiomyopathy patients are most commonly found in the A region; although truncations in the upstream I region might be expected to prevent translation of the A region entirely, alternative splicing creates some transcripts that do not encounter the premature stop codon, ameliorating its effect.[53] mRNA splicing factors such as RBM20 and SLM2 (KHDRBS3) were shown to mediated alternative mRNA splicing of titin mRNA contributing to the development of heart failure due to cardiomyopathies.[54][55]

Autoantibodies to titin are produced in patients with the autoimmune disease Myasthenia gravis.[56]

Interactions

Titin has been shown to interact with:

Linguistic significance

The name titin is derived from the Greek Titan (a giant deity, anything of great size).[5]

As the largest known protein, titin also has the longest IUPAC name of a protein. The full chemical name of the human canonical form of titin, which starts methionyl... and ends ...isoleucine, contains 189,819 letters and is sometimes stated to be the longest word in the English language, or of any language.[67] However, lexicographers regard generic names of chemical compounds as verbal formulae rather than English words.[68]

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    Further reading
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