Streptavidin/ˌstrɛpˈtævɪdɪn/is a 52kDaprotein(tetramer) purified from thebacteriumStreptomyces avidinii.Streptavidinhomo-tetramershave an extraordinarily high affinity forbiotin(also known as vitamin B7 or vitamin H). With adissociation constant(Kd) on the order of ≈10−14mol/L,[1]the binding of biotin to streptavidin is one of the strongest non-covalent interactions known in nature. Streptavidin is used extensively in molecular biology and bionanotechnology due to the streptavidin-biotin complex's resistance to organic solvents, denaturants (e.g.guanidinium chloride), detergents (e.g.SDS,Triton X-100), proteolytic enzymes, and extremes of temperature and pH.
Streptavidin | |||||||
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![]() Monomeric streptavidin (ribbon diagram) with bound biotin (spheres);PDB:1STP | |||||||
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UniProt | P22629 | ||||||
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Structure
editThe crystal structure of streptavidin with biotin bound was reported by two groups in 1989. The structure was solved using multi wavelength anomalous diffraction by Hendrickson et al.[2]atColumbia Universityand using multiple isomorphous replacement by Weber et al.[3]at E. I. DuPont Central Research and Development Department. As of September 2017, there are 171 structures deposited in theProtein Data Bank.Seethis linkfor a complete list. The N and C termini of the 159 residue full-length protein are processed to give a shorter ‘core’ streptavidin, usually composed of residues 13–139; removal of the N and C termini is necessary for the highest biotin-binding affinity. The secondary structure of a streptavidin monomer is composed of eight antiparallel β-strands, which fold to give an antiparallelβ-barreltertiary structure. Abiotinbinding-site is located at one end of each β-barrel. Four identical streptavidin monomers (i.e. four identical β-barrels) associate to give streptavidin's tetrameric quaternary structure. The biotin binding-site in each barrel consists of residues from the interior of the barrel, together with a conserved Trp120 from a neighboring subunit. In this way, each subunit contributes to the binding site on the neighboring subunit, and so the tetramer can also be considered a dimer of functional dimers.
Origins of the high affinity
editThe numerous crystal structures of the streptavidin-biotin complex have shed light on the origins of the remarkable affinity. Firstly, there is high shape-complementarity between the binding pocket and biotin. Secondly, there is an extensive network of hydrogen bonds formed to biotin when in the binding site. There are eighthydrogen bondsdirectly made to residues in the binding site (the so-called 'first shell' of hydrogen bonding), involving residues Asn23, Tyr43, Ser27, Ser45, Asn49, Ser88, Thr90 and Asp128. There is also a 'second shell' of hydrogen bonding involving residues that interact with the first shell residues. However, the streptavidin-biotin affinity exceeds that which would be predicted from the hydrogen bonding interactions alone, suggesting another mechanism contributing to the high affinity.[4]The biotin-binding pocket ishydrophobic,and there are numerousvan der Waals force-mediated contacts and hydrophobic interactions made to the biotin when in the pocket, which is also thought to account for the high affinity. In particular, the pocket is lined with conserved tryptophan residues. Lastly, biotin binding is accompanied by the stabilisation of a flexible loop connecting β-strands 3 and 4 (L3/4), which closes over the bound biotin, acting like a 'lid' over the binding pocket and contributing to the extremely slow biotin dissociation rate.
Most attempts at mutating streptavidin result in a lowered biotin-binding affinity, which is to be expected in such a highly optimized system. However, a recently engineered mutant of streptavidin, named traptavidin, was found to have more than ten-fold slower biotin dissociation, in addition to higher thermal and mechanical stability.[5]This decreased dissociation rate was accompanied by a two-fold decrease in the association rate.
Biotin-binding affinity can be impaired by chemical labeling of streptavidin, such as with amine-reactivefluorophores;flavidin is a streptavidin mutant without lysine side-chains, which retains good biotin binding characteristics after such fluorescent dye labeling where the dye couples to the amino terminus.[6]
Uses in biotechnology
editAmong the most common uses of streptavidin are the purification or detection of various biomolecules. The strong streptavidin-biotin interaction can be used to attach various biomolecules to one another or onto a solid support. Harsh conditions are needed to break the streptavidin-biotin interaction, which often denatures the protein of interest being purified. However, it has been shown that a short incubation in water above 70 °C will reversibly break the interaction (at least for biotinylated DNA) without denaturing streptavidin, allowing re-use of the streptavidin solid support.[7]A further application of streptavidin is for purification and detection of proteins genetically modified with theStrep-tagpeptide. Streptavidin is widely used inWestern blottingand immunoassays conjugated to some reporter molecule, such ashorseradish peroxidase. Streptavidin has also been used in the developing field ofNanobiotechnology,the use of biological molecules such as proteins or lipids to createnanoscaledevices/structures. In this context streptavidin can be used as a building block to link biotinylated DNA molecules to create single walledcarbon nanotubescaffolds[8]or even complex DNA polyhedra.[9] The tetrameric streptavidin has also been used as a hub around which other proteins may be arranged, either by an affinity tag such asStrep-tagorAviTagor by genetic fusion toSpyTag.[10]Fusion to SpyTag allowed generation of assemblies with 8 or 20 streptavidin subunits. As well as a molecular force probe foratomic force microscopystudies,[11]novel materials such as 3D crystalline lattices[12]have also been created. Streptavidin has a mildly acidicisoelectric point(pI) of ~5, but arecombinantform of streptavidin with a near-neutral pI is also commercially available.
- Pretargeted Immunotherapy
Pretargeted immunotherapy uses streptavidin conjugated to a monoclonal antibody against cancer cell-specific antigens followed by an injection of radiolabelled biotin to deliver the radiation only to the cancerous cell. Initial hurdles involve saturation of the biotin binding sites on streptavidin with endogenous biotin instead of the injected radiolabelled biotin, and a high degree of radioactive exposure in the kidneys due to streptavidin's strong cell adsorptive properties. It is currently thought that this high level of binding to adherent cell types, such as activated platelets and melanomas, is a result ofintegrinbinding mediated through the RYD sequence in streptavidin.[13]
Variants with a controlled number of binding sites
edit- Monovalent vs. monomeric
Streptavidin is a tetramer and each subunit binds biotin with equal affinity. Multivalency is an advantage in applications likeMHC tetramer staining,where avidity effects improve the ability of MHC molecules attached to streptavidin to detect specific T cells.[14]In other cases, such as the use of streptavidin for imaging specific proteins on cells, multivalency can perturb the function of the protein of interest. Monovalent streptavidin is an engineered recombinant form of streptavidin which is a tetramer but only one of the four binding sites is functional. This single binding site has 10−14mol/L affinity and cannot cause cross-linking.[15]Applications of monovalent streptavidin have included fluorescent tracking ofcell surface receptors,decoratingDNA origami,and acting as a pointer to identify specific regions forcryo-electron microscopy.
Monomeric streptavidin is a recombinant form of streptavidin with mutations to break the tetramer into a monomer and to enhance the solubility of the resultant isolated subunit. Monomeric streptavidin versions have an affinity for biotin of 10−7mol/L 10−8mol/L and so are not ideal for labeling applications but are useful for purification, where reversibility is desirable.[16][17]
- Divalent
A streptavidin with exactly two biotin binding sites per tetramer can be produced by mixing subunits with and without a functional biotin binding site and purification byion-exchange chromatography.The functional binding sites here have the same biotin binding stability as wild-type streptavidin. Divalent streptavidin with the two biotin binding sites together (cis-divalent) or apart (trans-divalent) can be separately purified.[18]
- Trivalent
A streptavidin with exactly three biotin binding sites per tetramer can also be produced using the same principle as to produce divalent streptavidins.[19]
- High-valency streptavidins
Streptavidins of higher valency has been obtained by utilizing the chemistry ofisopeptide bondconjugation using theSpyTag/SpyCatchertechnology.[20]This involves having a streptavidin tetramer with three biotin binding sites and a dead streptavidin fused to either SpyTag or SpyCatcher. When the different tetramers are mixed together, a covalent linkage occurs to enable higher number of biotin binding sites. Six and twelve biotin binding sites per molecule have been made with this method.
Comparison to avidin
editStreptavidin is not the only protein capable of binding to biotin with high affinity.Avidinis the other most notable biotin-binding protein. Originally isolated from egg yolk, avidin only has 30% sequence identity to streptavidin, but almost identical secondary, tertiary and quaternary structure. Avidin has a higher affinity for biotin (Kd~ 10−15M) but in contrast to streptavidin, avidin is glycosylated, positively charged, has pseudo-catalytic activity (avidin can enhance the alkaline hydrolysis of an ester linkage between biotin and a nitrophenyl group) and has a higher tendency for aggregation. On the other hand, streptavidin is the better biotin-conjugate binder; avidin has a lower binding affinity than streptavidin when biotin is conjugated to another molecule, despite avidin having the higher affinity for free, unconjugated biotin. Because streptavidin lacks anycarbohydratemodification and has a near-neutralpI,it has the advantage of much lowernonspecific bindingthan avidin.Deglycosylated avidin (NeutrAvidin)is more comparable to the size, pI, and nonspecific binding of streptavidin.
See also
editReferences
edit- ^Green NM (1975). "Avidin".Advances in Protein Chemistry.29:85–133.doi:10.1016/s0065-3233(08)60411-8.ISBN9780120342297.PMID237414.
- ^Hendrickson WA, Pähler A, Smith JL, Satow Y, Merritt EA, Phizackerley RP (April 1989)."Crystal structure of core streptavidin determined from multiwavelength anomalous diffraction of synchrotron radiation".Proceedings of the National Academy of Sciences of the United States of America.86(7): 2190–4.doi:10.1073/pnas.86.7.2190.PMC286877.PMID2928324.
- ^Weber PC, Ohlendorf DH, Wendoloski JJ, Salemme FR (January 1989). "Structural origins of high-affinity biotin binding to streptavidin".Science.243(4887): 85–8.doi:10.1126/science.2911722.PMID2911722.
- ^DeChancie J, Houk KN (May 2007)."The origins of femtomolar protein-ligand binding: hydrogen-bond cooperativity and desolvation energetics in the biotin-(strept)avidin binding site".Journal of the American Chemical Society.129(17): 5419–29.doi:10.1021/ja066950n.PMC2527462.PMID17417839.
- ^Chivers CE, Crozat E, Chu C, Moy VT, Sherratt DJ, Howarth M (May 2010)."A streptavidin variant with slower biotin dissociation and increased mechanostability".Nature Methods.7(5): 391–3.doi:10.1038/nmeth.1450.PMC2862113.PMID20383133.
- ^Jacobsen MT, Fairhead M, Fogelstrand P, Howarth M (August 2017)."Amine Landscaping to Maximize Protein-Dye Fluorescence and Ultrastable Protein-Ligand Interaction".Cell Chemical Biology.24(8): 1040–1047.e4.doi:10.1016/j.chembiol.2017.06.015.PMC5563079.PMID28757182.
- ^Holmberg A, Blomstergren A, Nord O, Lukacs M, Lundeberg J, Uhlén M (February 2005). "The biotin-streptavidin interaction can be reversibly broken using water at elevated temperatures".Electrophoresis.26(3): 501–10.doi:10.1002/elps.200410070.PMID15690449.S2CID16058388.
- ^Ostojic GN, Hersam MC (June 2012). "Biomolecule-directed assembly of self-supported, nanoporous, conductive, and luminescent single-walled carbon nanotube scaffolds".Small.8(12): 1840–5.doi:10.1002/smll.201102536.PMID22461319.
- ^Zhang C, Tian C, Guo F, Liu Z, Jiang W, Mao C (April 2012). "DNA-directed three-dimensional protein organization".Angewandte Chemie.51(14): 3382–5.doi:10.1002/anie.201108710.PMID22374892.
- ^Fairhead M, Veggiani G, Lever M, Yan J, Mesner D, Robinson CV, Dushek O, van der Merwe PA, Howarth M (September 2014)."SpyAvidin hubs enable precise and ultrastable orthogonal nanoassembly".Journal of the American Chemical Society.136(35): 12355–63.doi:10.1021/ja505584f.PMC4183622.PMID25111182.
- ^Kim M, Wang CC, Benedetti F, Marszalek PE (February 2012)."A nanoscale force probe for gauging intermolecular interactions".Angewandte Chemie.51(8): 1903–6.doi:10.1002/anie.201107210.PMC3279624.PMID22253141.
- ^Sinclair JC, Davies KM, Vénien-Bryan C, Noble ME (July 2011). "Generation of protein lattices by fusing proteins with matching rotational symmetry".Nature Nanotechnology.6(9): 558–62.doi:10.1038/nnano.2011.122.PMID21804552.
- ^Alon R, Bayer EA, Wilchek M (August 1992). "Cell-adhesive properties of streptavidin are mediated by the exposure of an RGD-like RYD site".European Journal of Cell Biology.58(2): 271–9.PMID1425765.
- ^Xu XN, Screaton GR (October 2002). "MHC/peptide tetramer-based studies of T cell function".Journal of Immunological Methods.268(1): 21–8.doi:10.1016/S0022-1759(02)00196-5.PMID12213339.
- ^Howarth M, Chinnapen DJ, Gerrow K, Dorrestein PC, Grandy MR, Kelleher NL, El-Husseini A, Ting AY (April 2006)."A monovalent streptavidin with a single femtomolar biotin binding site".Nature Methods.3(4): 267–73.doi:10.1038/nmeth861.PMC2576293.PMID16554831.
- ^Wu SC, Wong SL (June 2005)."Engineering soluble monomeric streptavidin with reversible biotin binding capability".The Journal of Biological Chemistry.280(24): 23225–31.doi:10.1074/jbc.M501733200.PMID15840576.
- ^Lim KH, Huang H, Pralle A, Park S (October 2011). "Engineered streptavidin monomer and dimer with improved stability and function".Biochemistry.50(40): 8682–91.doi:10.1021/bi2010366.PMID21892837.
- ^Fairhead M, Krndija D, Lowe ED, Howarth M (January 2014)."Plug-and-play pairing via defined divalent streptavidins".Journal of Molecular Biology.426(1): 199–214.doi:10.1016/j.jmb.2013.09.016.PMC4047826.PMID24056174.
- ^Dubacheva, Galina V.; Araya-Callis, Carolina; Geert Volbeda, Anne; Fairhead, Michael; Codée, Jeroen; Howarth, Mark; Richter, Ralf P. (9 March 2017)."Controlling Multivalent Binding through Surface Chemistry: Model Study on Streptavidin".Journal of the American Chemical Society.139(11): 4157–4167.doi:10.1021/jacs.7b00540.PMC5364436.PMID28234007.
- ^Fairhead, Michael; Veggiani, Gianluca; Lever, Melissa; Yan, Jun; Mesner, Dejan; Robinson, Carol V.; Dushek, Omer; van der Merwe, P. Anton; Howarth, Mark (21 August 2014)."SpyAvidin Hubs Enable Precise and Ultrastable Orthogonal Nanoassembly".Journal of the American Chemical Society.136(35): 12355–12363.doi:10.1021/ja505584f.PMC4183622.PMID25111182.
Further reading
edit- Hutchens TW, Porath JO (September 1987)."Protein recognition of immobilized ligands: promotion of selective adsorption".Clinical Chemistry.33(9): 1502–8.doi:10.1093/clinchem/33.9.1502.PMID3621554.
- Chodosh LA, Buratowski S (2001). "Purification of DNA-Binding Proteins Using Biotin/Streptavidin Affinity Systems".Current Protocolsin Protein Science.Vol. Chapter 9. 9.7.1–9.7.13.doi:10.1002/0471140864.ps0907s12.ISBN978-0-471-14086-3.PMID18429216.S2CID23660759.
- Zimmermann RM, Cox EC (February 1994)."DNA stretching on functionalized gold surfaces".Nucleic Acids Research.22(3): 492–7.doi:10.1093/nar/22.3.492.PMC523609.PMID8127690.
External links
edit- Swiss-Prot entry for Streptavidin precursor fromStreptomyces avidinii
- Streptavidinat the U.S. National Library of MedicineMedical Subject Headings(MeSH)
- Egg-stremely useful interactionQUite Interesting PDB Structure article atPDBe
Groups investigating and developing streptavidin or avidin-family proteins (Alphabetical order)