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Protein quaternary structure

(Redirected from Multiprotein complexes)

Protein quaternary structure[a] is the fourth (and highest) classification level of protein structure. Protein quaternary structure refers to the structure of proteins which are themselves composed of two or more smaller protein chains (also referred to as subunits). Protein quaternary structure describes the number and arrangement of multiple folded protein subunits in a multi-subunit complex. It includes organizations from simple dimers to large homooligomers and complexes with defined or variable numbers of subunits.[1] In contrast to the first three levels of protein structure, not all proteins will have a quaternary structure since some proteins function as single units. Protein quaternary structure can also refer to biomolecular complexes of proteins with nucleic acids and other cofactors.

Protein primary structureProtein secondary structureProtein tertiary structureProtein quaternary structure
The image above contains clickable links
The image above contains clickable links
This diagram (which is interactive) of protein structure uses PCNA as an example. (PDB: 1AXC​)
This article is about quaternary structure in protein. For the article about quaternary structure in nucleic acid, see Nucleic acid quaternary structure.

Description and examples

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Many proteins are actually assemblies of multiple polypeptide chains. The quaternary structure refers to the number and arrangement of the protein subunits with respect to one another.[2] Examples of proteins with quaternary structure include hemoglobin, DNA polymerase, ribosomes, antibodies, and ion channels.

Enzymes composed of subunits with diverse functions are sometimes called holoenzymes, in which some parts may be known as regulatory subunits and the functional core is known as the catalytic subunit. Other assemblies referred to instead as multiprotein complexes also possess quaternary structure. Examples include nucleosomes and microtubules. Changes in quaternary structure can occur through conformational changes within individual subunits or through reorientation of the subunits relative to each other. It is through such changes, which underlie cooperativity and allostery in "multimeric" enzymes, that many proteins undergo regulation and perform their physiological function.

The above definition follows a classical approach to biochemistry, established at times when the distinction between a protein and a functional, proteinaceous unit was difficult to elucidate. More recently, people refer to protein–protein interaction when discussing quaternary structure of proteins and consider all assemblies of proteins as protein complexes.

Nomenclature

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The quaternary structure of this protein complex would be described as a homo-trimer because it is composed of three identical smaller protein subunits (also designated as monomers or protomers).

The number of subunits in an oligomeric complex is described using names that end in -mer (Greek for "part, subunit"). Formal and Greco-Latinate names are generally used for the first ten types and can be used for up to twenty subunits, whereas higher order complexes are usually described by the number of subunits, followed by -meric.

  • 13 = tridecamer
  • 14 = tetradecamer
  • 15 = pentadecamer*
  • 16 = hexadecamer
  • 17 = heptadecamer*
  • 18 = octadecamer
  • 19 = nonadecamer
  • 20 = eicosamer
  • 21 = 21-mer
  • 22 = 22-mer
  • 23 = 23-mer*
  • etc.
*No known examples

The smallest unit forming a homo-oligomer, i.e. one protein chain or subunit, is designated as a monomer, subunit or protomer. The latter term was originally devised to specify the smallest unit of hetero-oligomeric proteins, but is also applied to homo-oligomeric proteins in current literature. The subunits usually arrange in cyclic symmetry to form closed point group symmetries.

Although complexes higher than octamers are rarely observed for most proteins, there are some important exceptions. Viral capsids are often composed of multiples of 60 proteins. Several molecular machines are also found in the cell, such as the proteasome (four heptameric rings = 28 subunits), the transcription complex and the spliceosome. The ribosome is probably the largest molecular machine, and is composed of many RNA and protein molecules.

In some cases, proteins form complexes that then assemble into even larger complexes. In such cases, one uses the nomenclature, e.g., "dimer of dimers" or "trimer of dimers". This may suggest that the complex might dissociate into smaller sub-complexes before dissociating into monomers. This usually implies that the complex consists of different oligomerisation interfaces. For example, a tetrameric protein may have one four-fold rotation axis, i.e. point group symmetry 4 or C4. In this case the four interfaces between the subunits are identical. It may also have point group symmetry 222 or D2. This tetramer has different interfaces and the tetramer can dissociate into two identical homodimers. Tetramers of 222 symmetry are "dimer of dimers". Hexamers of 32 point group symmetry are "trimer of dimers" or "dimer of trimers". Thus, the nomenclature "dimer of dimers" is used to specify the point group symmetry or arrangement of the oligomer, independent of information relating to its dissociation properties.

Another distinction often made when referring to oligomers is whether they are homomeric or heteromeric, referring to whether the smaller protein subunits that come together to make the protein complex are the same (homomeric) or different (heteromeric) from each other. For example, two identical protein monomers would come together to form a homo-dimer, whereas two different protein monomers would create a hetero-dimer.

Structure Determination

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Protein quaternary structure can be determined using a variety of experimental techniques that require a sample of protein in a variety of experimental conditions. The experiments often provide an estimate of the mass of the native protein and, together with knowledge of the masses and/or stoichiometry of the subunits, allow the quaternary structure to be predicted with a given accuracy. It is not always possible to obtain a precise determination of the subunit composition for a variety of reasons.

The number of subunits in a protein complex can often be determined by measuring the hydrodynamic molecular volume or mass of the intact complex, which requires native solution conditions. For folded proteins, the mass can be inferred from its volume using the partial specific volume of 0.73 ml/g. However, volume measurements are less certain than mass measurements, since unfolded proteins appear to have a much larger volume than folded proteins; additional experiments are required to determine whether a protein is unfolded or has formed an oligomer.

Common techniques used to study protein quaternary structure

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  • Ultracentrifugation
  • Surface-induced dissociation mass spectrometry[3]
  • Coimmunoprecipation[4]
  • FRET[4][5]
  • Nuclear Magnetic Resonance (NMR)[6][7]

Direct mass measurement of intact complexes

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Direct size measurement of intact complexes

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Indirect size measurement of intact complexes

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Methods that measure the mass or volume under unfolding conditions (such as MALDI-TOF mass spectrometry and SDS-PAGE) are generally not useful, since non-native conditions usually cause the complex to dissociate into monomers. However, these may sometimes be applicable; for example, the experimenter may apply SDS-PAGE after first treating the intact complex with chemical cross-link reagents.

Structure Prediction

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Some bioinformatics methods have been developed for predicting the quaternary structural attributes of proteins based on their sequence information by using various modes of pseudo amino acid composition.[2][8][9]

Protein folding prediction programs used to predict protein tertiary structure have also been expanding to better predict protein quaternary structure. One such development is AlphaFold-Multimer[10] built upon the AlphaFold model for predicting protein tertiary structure.

Role in Cell Signaling

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Protein quaternary structure also plays an important role in certain cell signaling pathways. The G-protein coupled receptor pathway involves a heterotrimeric protein known as a G-protein. G-proteins contain three distinct subunits known as the G-alpha, G-beta, and G-gamma subunits. When the G-protein is activated, it binds to the G-protein coupled receptor protein and the cell signaling pathway is initiated. Another example is the receptor tyrosine kinase (RTK) pathway, which is initiated by the dimerization of two receptor tyrosine kinase monomers. When the dimer is formed, the two kinases can phosphorylate each other and initiate a cell signaling pathway.[11]

Protein–protein interactions

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Main article: Protein–protein interaction

Proteins are capable of forming very tight but also only transient complexes. For example, ribonuclease inhibitor binds to ribonuclease A with a roughly 20 fM dissociation constant. Other proteins have evolved to bind specifically to unusual moieties on another protein, e.g., biotin groups (avidin), phosphorylated tyrosines (SH2 domains) or proline-rich segments (SH3 domains). Protein–protein interactions can be engineered to favor certain oligomerization states.[12]

Intragenic complementation

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When multiple copies of a polypeptide encoded by a gene form a quaternary complex, this protein structure is referred to as a multimer.[13] When a multimer is formed from polypeptides produced by two different mutant alleles of a particular gene, the mixed multimer may exhibit greater functional activity than the unmixed multimers formed by each of the mutants alone. In such a case, the phenomenon is referred to as intragenic complementation (also called inter-allelic complementation). Intragenic complementation appears to be common and has been studied in many different genes in a variety of organisms including the fungi Neurospora crassa, Saccharomyces cerevisiae and Schizosaccharomyces pombe; the bacterium Salmonella typhimurium; the virus bacteriophage T4,[14] an RNA virus,[15] and humans.[16] The intermolecular forces likely responsible for self-recognition and multimer formation were discussed by Jehle.[17]

Assembly

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Direct interaction of two nascent proteins emerging from nearby ribosomes appears to be a general mechanism for oligomer formation.[18] Hundreds of protein oligomers were identified that assemble in human cells by such an interaction.[18] The most prevalent form of interaction was between the N-terminal regions of the interacting proteins. Dimer formation appears to be able to occur independently of dedicated assembly machines.

See also

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Notes

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  1. ^ Here quaternary means "fourth-level structure", not "four-way interaction". Etymologically quartary is correct: quaternary is derived from Latin distributive numbers, and follows binary and ternary; while quartary is derived from Latin ordinal numbers, and follows secondary and tertiary. However, quaternary is standard in biology.

References

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  1. ^ Berg JM, Tymoczko JL, Stryer L (2002). "Section 3.5Quaternary Structure: Polypeptide Chains Can Assemble Into Multisubunit Structures". Biochemistry (5. ed., 4. print. ed.). New York, NY [u.a.]: W. H. Freeman. ISBN 0-7167-3051-0.
  2. ^ a b Chou KC, Cai YD (November 2003). "Predicting protein quaternary structure by pseudo amino acid composition". Proteins. 53 (2): 282–289. doi:10.1002/prot.10500. PMID 14517979. S2CID 23979933.
  3. ^ Stiving AQ, VanAernum ZL, Busch F, Harvey SR, Sarni SH, Wysocki VH (January 2019). "Surface-Induced Dissociation: An Effective Method for Characterization of Protein Quaternary Structure". review. Analytical Chemistry. 91 (1): 190–209. doi:10.1021/acs.analchem.8b05071. PMC 6571034. PMID 30412666.
  4. ^ a b Milligan G, Bouvier M (June 2005). "Methods to monitor the quaternary structure of G protein-coupled receptors". review. The FEBS Journal. 272 (12): 2914–2925. doi:10.1111/j.1742-4658.2005.04731.x. PMID 15955052. S2CID 23274563.
  5. ^ Raicu V, Singh DR (November 2013). "FRET spectrometry: a new tool for the determination of protein quaternary structure in living cells". primary. Biophysical Journal. 105 (9): 1937–1945. Bibcode:2013BpJ...105.1937R. doi:10.1016/j.bpj.2013.09.015. PMC 3824708. PMID 24209838.
  6. ^ Prischi F, Pastore A (2016). "Application of Nuclear Magnetic Resonance and Hybrid Methods to Structure Determination of Complex Systems". Advanced Technologies for Protein Complex Production and Characterization. review. Advances in Experimental Medicine and Biology. Vol. 896. pp. 351–368. doi:10.1007/978-3-319-27216-0_22. ISBN 978-3-319-27214-6. PMID 27165336.
  7. ^ Wells JN, Marsh JA (2018). "Experimental Characterization of Protein Complex Structure, Dynamics, and Assembly". Protein Complex Assembly. review. Methods in Molecular Biology. Vol. 1764. pp. 3–27. doi:10.1007/978-1-4939-7759-8_1. ISBN 978-1-4939-7758-1. PMID 29605905. Section 4: Nuclear Magnetic Resonance Spectroscopy
  8. ^ Zhang SW, Chen W, Yang F, Pan Q (October 2008). "Using Chou's pseudo amino acid composition to predict protein quaternary structure: a sequence-segmented PseAAC approach". Amino Acids. 35 (3): 591–598. doi:10.1007/s00726-008-0086-x. PMID 18427713. S2CID 689955.
  9. ^ Xiao X, Wang P, Chou KC (2009). "Predicting protein quaternary structural attribute by hybridizing functional domain composition and pseudo amino acid composition". Journal of Applied Crystallography. 42: 169–173. doi:10.1107/S0021889809002751.
  10. ^ Evans R, O'Neill M, Pritzel A, Antropova N, Senior AW, Green T, et al. (4 October 2021). "Protein complex prediction with AlphaFold-Multimer". bioRxiv: 2021.10.04.463034. doi:10.1101/2021.10.04.463034. S2CID 238413014.
  11. ^ Heldin CH (January 1995). "Dimerization of cell surface receptors in signal transduction". Cell. 80 (2): 213–223. doi:10.1016/0092-8674(95)90404-2. PMID 7834741. S2CID 18925209.
  12. ^ Ardejani MS, Chok XL, Foo CJ, Orner BP (May 2013). "Complete shift of ferritin oligomerization toward nanocage assembly via engineered protein-protein interactions". Chemical Communications. 49 (34): 3528–3530. doi:10.1039/C3CC40886H. PMID 23511498.
  13. ^ Crick FH, Orgel LE (January 1964). "The theory of inter-allelic complementation". Journal of Molecular Biology. 8: 161–165. doi:10.1016/s0022-2836(64)80156-x. PMID 14149958.
  14. ^ Bernstein H, Edgar RS, Denhardt GH (June 1965). "Intragenic complementation among temperature sensitive mutants of bacteriophage T4D". Genetics. 51 (6): 987–1002. doi:10.1093/genetics/51.6.987. PMC 1210828. PMID 14337770.
  15. ^ Smallwood S, Cevik B, Moyer SA (December 2002). "Intragenic complementation and oligomerization of the L subunit of the sendai virus RNA polymerase". Virology. 304 (2): 235–245. doi:10.1006/viro.2002.1720. PMID 12504565.
  16. ^ Rodríguez-Pombo P, Pérez-Cerdá C, Pérez B, Desviat LR, Sánchez-Pulido L, Ugarte M (June 2005). "Towards a model to explain the intragenic complementation in the heteromultimeric protein propionyl-CoA carboxylase". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1740 (3): 489–498. doi:10.1016/j.bbadis.2004.10.009. PMID 15949719.
  17. ^ Jehle H (September 1963). "Intermolecular forces and biological specificity". Proceedings of the National Academy of Sciences of the United States of America. 50 (3): 516–524. Bibcode:1963PNAS...50..516J. doi:10.1073/pnas.50.3.516. PMC 221211. PMID 16578546.
  18. ^ a b Bertolini M, Fenzl K, Kats I, Wruck F, Tippmann F, Schmitt J, et al. (January 2021). "Interactions between nascent proteins translated by adjacent ribosomes drive homomer assembly". primary. Science. 371 (6524): 57–64. Bibcode:2021Sci...371...57B. doi:10.1126/science.abc7151. PMC 7613021. PMID 33384371. S2CID 229935047.
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