Abstract
Nuclear magnetic resonance spectroscopy studies of ever larger systems have benefited from many different forms of isotope labeling, in particular, site specific isotopic labeling. Site specific 13C labeling of methyl groups has become an established means of probing systems not amenable to traditional methodology. However useful, methyl reporter sites can be limited in number and/or location. Therefore, new complementary site specific isotope labeling strategies are valuable. Aromatic amino acids make excellent probes since they are often found at important interaction interfaces and play significant structural roles. Aromatic side chains have many of the same advantages as methyl containing amino acids including distinct 13C chemical shifts and multiple magnetically equivalent 1H positions. Herein we report economical bacterial production and one-step purification of phenylalanine with 13C incorporation at the Cα, Cγ and Cε positions, resulting in two isolated 1H-13C spin systems. We also present methodology to maximize incorporation of phenylalanine into recombinantly overexpressed proteins in bacteria and demonstrate compatibility with ILV-methyl labeling. Inexpensive, site specific isotope labeled phenylalanine adds another dimension to biomolecular NMR, opening new avenues of study.
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References
Babu CR, Flynn PF, Wand AJ (2001) Validation of protein structure from preparations of encapsulated proteins dissolved in low viscosity fluids. J Am Chem Soc 123(11):2691–2692
Baez-Viveros JL, Osuna J, Hernandez-Chavez G, Soberon X, Bolivar F, Gosset G (2004) Metabolic engineering and protein directed evolution increase the yield of l-phenylalanine synthesized from glucose in Escherichia coli. Biotechnol Bioeng 87:516–524. doi:10.1002/bit.20159
Barker JL, Frost JW (2001) Microbial synthesis of p-hydroxybenzoic acid from glucose. Biotechnol Bioeng 76:376–390. doi:10.1002/bit.10160
Ben-Shimon A, Eisenstein M (2010) Computational mapping of anchoring spots on protein surfaces. J Mol Biol 402:259–277. doi:10.1016/j.jmb.2010.07.021
Bogan AA, Thorn KS (1998) Anatomy of hot spots in protein interfaces. J Mol Biol 280:1–9. doi:10.1006/jmbi.1998.1843
Boyer JA, Lee AL (2008) Monitoring aromatic picosecond to nanosecond dynamics in proteins via 13C relaxation: expanding perturbation mapping of the rigidifying core mutation, V54A, in eglin c. biochemistry 47:4876–4886. doi:10.1021/bi702330t
Butterfield SM, Patel PR, Waters ML (2002) Contribution of aromatic interactions to α-helix stability. J Am Chem Soc 124:9751–9755. doi:10.1021/ja026668q
Casteleijn MG, Urtti A, Sarkhel S (2013) Expression without boundaries: cell-free protein synthesis in pharmaceutical research. Int J Pharm 440:39–47. doi:10.1016/j.ijpharm.2012.04.005
Chavez MI et al (2005) On the importance of carbohydrate-aromatic interactions for the molecular recognition of oligosaccharides by proteins: NMR studies of the structure and binding affinity of AcAMP2-like peptides with non-natural naphthyl and fluoroaromatic residues. Chemistry 11:7060–7074. doi:10.1002/chem.200500367
Churchill CD, Rutledge LR, Wetmore SD (2010) Effects of the biological backbone on stacking interactions at DNA–protein interfaces: the interplay between the backbone... π and π...π components. Phys Chem Chem Phys 12:14515–14526 doi:10.1039/c0cp00550a
Duan G, Smith VH, Weaver DF (2000) Characterization of aromatic-amide (side-chain) interactions in proteins through systematic ab initio calculations and data mining analyses. J Phys Chem A 104:4521–4532. doi:10.1021/jp993381f
Fischer M, Kloiber K, Hausler J, Ledolter K, Konrat R, Schmid W (2007) Synthesis of a 13C-methyl-group-labeled methionine precursor as a useful tool for simplifying protein structural analysis by NMR spectroscopy. Chembiochem 8:610–612. doi:10.1002/cbic.200600551
Gardner KH, Rosen MK, Kay LE (1997) Global folds of highly deuterated, methyl-protonated proteins by multidimensional NMR. Biochemistry 36:1389–1401. doi:10.1021/bi9624806bi9624806
Gelis I et al (2007) Structural basis for signal-sequence recognition by the translocase motor SecA as determined by NMR. Cell 131:756–769. doi:10.1016/j.cell.2007.09.039
Giorgi L et al (2011) NMR-based substrate analog docking to Escherichia coli peptidyl-tRNA hydrolase. J Mol Biol 412:619–633. doi:10.1016/j.jmb.2011.06.025
Hudson KL, Bartlett GJ, Diehl RC, Agirre J, Gallagher T, Kiessling LL, Woolfson DN (2015) Carbohydrate-aromatic interactions in proteins. J Am Chem Soc 137:15152–15160. doi:10.1021/jacs.5b08424
Hughes RC, McFeeters H, Coates L, McFeeters RL (2012) Recombinant production, crystallization and X-ray crystallographic structure determination of the peptidyl-tRNA hydrolase of Pseudomonas aeruginosa. Acta Crystallogr Sect F Struct Biol Cryst Commun 68:1472–1476. doi:10.1107/S1744309112045770
Ikeda M (2006) Towards bacterial strains overproducing l-tryptophan and other aromatics by metabolic engineering. Appl Microbiol Biotechnol 69:615–626. doi:10.1007/s00253-005-0252-y
Ikeda M, Katsumata R (1992) Metabolic engineering to produce tyrosine or phenylalanine in a tryptophan-producing corynebacterium glutamicum strain. Appl Environ Microbiol 58:781–785
Kasinath V, Valentine KG, Wand AJ (2013) A 13C labeling strategy reveals a range of aromatic side chain motion in calmodulin. J Am Chem Soc 135:9560–9563. doi:10.1021/ja4001129
Kleckner IR, Foster MP (2011) An introduction to NMR-based approaches for measuring protein dynamics. Biochim Biophys Acta 1814:942–968. doi:10.1016/j.bbapap.2010.10.012
Krishnarjuna B, Jaipuria G, Thakur A, D’Silva P, Atreya HS (2011) Amino acid selective unlabeling for sequence specific resonance assignments in proteins. J Biomol NMR 49:39–51. doi:10.1007/s10858-010-9459-z
Lange OF et al (2008) Recognition dynamics up to microseconds revealed from an RDC-derived ubiquitin ensemble in solution. Science 320:1471–1475. doi:10.1126/science.1157092
LeMaster DM, Cronan JE Jr (1982) Biosynthetic production of 13C-labeled amino acids with site-specific enrichment. J Biol Chem 257:1224–1230
LeMaster DM, Richards FM (1982) Preparative-scale isolation of isotopically labeled amino acids. Anal Biochem 122:238–247
Lichtenecker RJ (2014) Synthesis of aromatic (13)C/(2)H-α-ketoacid precursors to be used in selective phenylalanine and tyrosine protein labelling. Org Biomol Chem 12:7551–7560. doi:10.1039/c4ob01129e
Lichtenecker RJ, Weinhaupl K, Schmid W, Konrat R (2013) α-Ketoacids as precursors for phenylalanine and tyrosine labelling in cell-based protein overexpression. J Biomol NMR 57:327–331. doi:10.1007/s10858-013-9796-9
Lundstrom P et al (2007) Fractional 13 C enrichment of isolated carbons using [1-13C]- or [2-13C]-glucose facilitates the accurate measurement of dynamics at backbone Cα and side-chain methyl positions in proteins. J Biomol NMR 38:199–212. doi:10.1007/s10858-007-9158-6
Lutke-Eversloh T, Stephanopoulos G (2008) Combinatorial pathway analysis for improved l-tyrosine production in Escherichia coli: identification of enzymatic bottlenecks by systematic gene overexpression. Metab Eng 10:69–77. doi:10.1016/j.ymben.2007.12.001
Madhusudan Makwana K, Mahalakshmi R (2015) Implications of aromatic-aromatic interactions: from protein structures to peptide models. Protein Sci 24:1920–1933. doi:10.1002/pro.2814
Maniatis T, Sambrook J (1982) Molecular cloning: a laboratory manual 1st edn. Cold Spring Harbor Laboratory, Cold Spring Harbor
McCaldon P, Argos P (1988) Oligopeptide biases in protein sequences and their use in predicting protein coding regions in nucleotide sequences. Proteins 4:99–122. doi:10.1002/prot.340040204
McFeeters RL (2002) Backbone chemical shift assignments and dynamics characteriation of an extracellular ligand-binding domain form an iontoroic glutamate receptor. Cornell University, Ithaca
McFeeters RL, Altieri AS, Cherry S, Tropea JE, Waugh DS, Byrd RA (2007a) The high-precision solution structure of Yersinia modulating protein YmoA provides insight into interaction with H-NS. Biochemistry 46:13975–13982. doi:10.1021/bi701210j
McFeeters RL et al (2007b) The novel fold of scytovirin reveals a new twist for antiviral entry inhibitors. J Mol Biol 369:451–461. doi:10.1016/j.jmb.2007.03.030
McFeeters H, Gilbert MJ, Thompson RM, Setzer WN, Cruz-Vera LR, McFeeters RL (2012) Inhibition of essential bacterial peptidyl-tRNA hydrolase activity by tropical plant extracts. Nat Prod Commun 7:1107–1110
Miyanoiri Y, Ishida Y, Takeda M, Terauchi T, Inouye M, Kainosho M (2016) Highly efficient residue-selective labeling with isotope-labeled Ile, Leu, and Val using a new auxotrophic E. coli strain. J Biomol NMR 65:109–119. doi:10.1007/s10858-016-0042-0
Oh MK, Rohlin L, Kao KC, Liao JC (2002) Global expression profiling of acetate-grown Escherichia coli. J Biol Chem 277:13175–13183. doi:10.1074/jbc.M110809200M110809200
Rajesh S, Nietlispach D, Nakayama H, Takio K, Laue ED, Shibata T, Ito Y (2003) A novel method for the biosynthesis of deuterated proteins with selective protonation at the aromatic rings of Phe, Tyr and Trp. J Biomol NMR 27:81–86
Rittmann D, Lindner SN, Wendisch VF (2008) Engineering of a glycerol utilization pathway for amino acid production by Corynebacterium glutamicum. Appl Environ Microbiol 74:6216–6222. doi:10.1128/AEM.00963-08
Rosen MK, Gardner KH, Willis RC, Parris WE, Pawson T, Kay LE (1996) Selective methyl group protonation of perdeuterated proteins. J Mol Biol 263:627–636. doi:10.1006/jmbi.1996.0603
Santos CN, Stephanopoulos G (2008) Melanin-based high-throughput screen for l-tyrosine production in Escherichia coli. Appl Environ Microbiol 74:1190–1197. doi:10.1128/AEM.02448-07
Schneider HJ (2009) Binding mechanisms in supramolecular complexes. Angew Chem Int Ed Engl 48:3924–3977. doi:10.1002/anie.200802947
Shortle D (1994) Assignment of amino acid type in 1H-15N correlation spectra by labeling with 14N-amino acids. J Magn Reson Ser B 105:88–90
Sinha K, Jen-Jacobson L, Rule GS (2011) Specific labeling of threonine methyl groups for NMR studies of protein-nucleic acid complexes. Biochemistry 50:10189–10191. doi:10.1021/bi201496d
Sprenger GA (2007) From scratch to value: engineering Escherichia coli wild type cells to the production of l-phenylalanine and other fine chemicals derived from chorismate. Appl Microbiol Biotechnol 75:739–749. doi:10.1007/s00253-007-0931-y
Taylor-Creel K, Hames MC, Holloway WB, McFeeters H, McFeeters RL (2014) Expression, purification, and solubility optimization of peptidyl-tRNA hydrolase 1 from Bacillus cereus. Protein Expr Purif 95:259–264. doi:10.1016/j.pep.2014.01.007
Teilum K, Brath U, Lundstrom P, Akke M (2006) Biosynthetic 13C labeling of aromatic side chains in proteins for NMR relaxation measurements. J Am Chem Soc 128:2506–2507. doi:10.1021/ja055660o
Thongchuang M, Pongsawasdi P, Chisti Y, Packdibamrung K (2012) Design of a recombinant Escherichia coli for producing l-phenylalanine from glycerol. World J Microbiol Biotechnol 28:2937–2943. doi:10.1007/s11274-012-1104-4
Tong KI, Yamamoto M, Tanaka T (2008) A simple method for amino acid selective isotope labeling of recombinant proteins in E. coli. J Biomol NMR 42:59–67. doi:10.1007/s10858-008-9264-0
Tugarinov V, Kay LE (2003) Ile, Leu, and Val methyl assignments of the 723-residue malate synthase G using a new labeling strategy and novel NMR methods. J Am Chem Soc 125:13868–13878. doi:10.1021/ja030345s
Wand AJ, Bieber RJ, Urbauer JL, McEvoy RP, Gan Z (1995) Carbon relaxation in randomly fractionally 13C-enriched proteins. J Magn Reson B 108:173–175
Wang H, Janowick DA, Schkeryantz JM, Liu X, Fesik SW (1999) A method for assigning phenylalanines in proteins. J Am Chem Soc 121:1611–1612. doi:10.1021/ja983897x
Wang J, Liu L, Zhou H, Li J, Du G, Chen J (2011) Comparative study of l-phenylalanine production in the growing and stationary phases during high cell density cultivation of an auxotrophic Escherichia coli. Biotechnol Bioprocess Eng 16:916–922. doi:10.1007/s12257-011-0135-2
Wilson RC, Edmondson SP, Flatt JW, Helms K, Twigg PD (2011) The E2-25K ubiquitin-associated (UBA) domain aids in polyubiquitin chain synthesis and linkage specificity. Biochem Biophys Res Commun 405:662–666 doi:10.1016/j.bbrc.2011.01.089
Zhang G, Neubert TA (2009) Use of stable isotope labeling by amino acids in cell culture (SILAC) for phophotyrosine protein identification and quantitation. Methods Mol Biol 527:79–92
Zhou H, Liao X, Liu L, Wang T, Du G, Chen J (2010) Enhanced L-phenylalanine production by recombinant Escherichia coli BR-42 (pAP-B03) resistant to bacteriophage BP-1 via a two-stage feeding approach. J Ind Microbiol Biotechnol 38:1219–1227. doi:10.1007/s10295-010-0900-9
Acknowledgements
Research reported in this publication was supported by the NIGMS of the National Institute of Health under Award Number 1R15GM093912. The authors thank Mary Hames for cloning and molecular biology support.
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Ramaraju, B., McFeeters, H., Vogler, B. et al. Bacterial production of site specific 13C labeled phenylalanine and methodology for high level incorporation into bacterially expressed recombinant proteins. J Biomol NMR 67, 23–34 (2017). https://doi.org/10.1007/s10858-016-0081-6
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DOI: https://doi.org/10.1007/s10858-016-0081-6
Keywords
- Site specific isotope labeling
- Phenylalanine
- Aromatic amino acids
- NMR spectroscopy
- Isolated 1H-13C spin systems
- Stable isotope incorporation