Bryostatin

Bryostatins are a group of macrolide lactones from the marine organism Bugula neritina that were first collected and provided to JL Hartwell’s anticancer drug discovery group at the National Cancer Institute (NCI) by Jack Rudloe.[1] Bryostatins are potent modulators of protein kinase C. They have been studied in clinical trials as anti-cancer agents, as anti-AIDS/HIV agents and in people with Alzheimer's disease.

Bryostatin 1
Names
IUPAC name
(1S,3S,5Z,7R,8E,11S,12S,13E,15S,17R,20R,23R,25S)-25-Acetoxy-1,11,20-trihydroxy-17-[(1R)-1-hydroxyethyl]-5,13-bis(2-methoxy-2-oxoethylidene)-10,10,26,26-tetramethyl-19-oxo-18,27,28,29-tetraoxatetracyclo[21.3.1.13,7.111,15]nonacos-8-en-12-yl (2E,4E)-2,4-octadienoate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
KEGG
UNII
Properties
C47H68O17
Molar mass 905.044 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Biological effects

Bryostatin 1 is a potent modulator of protein kinase C (PKC).[2]

It showed activity in laboratory tests in cells and model animals, so it was brought into clinical trials. As of 2014 over thirty clinical trials had been conducted, using bryostatin alone and in combination with other agents, in both solid tumors and blood tumors; it did not show a good enough risk:benefit ratio to be advanced further.[3]

It showed enough promise in animal models of Alzheimer's disease that a Phase II trial was started by 2010;[4] the trial was sponsored by the Blanchette Rockefeller Neurosciences Institute.[5] Scientists from that institute started a company called Neurotrope,[6] and launched another clinical trial in Alzheimer's disease,[7] preliminary results of which were released in 2017. [8][9]

Bryostatin has also been studied in people with HIV.[2]

Chemistry

Bryostatin 1 was first isolated in the 1960s by George Pettit from extracts of a species of bryozoan, Bugula neritina, based on research from samples originally provided by Jack Rudloe to Jonathan L. Hartwell’s anticancer drug discovery group at the National Cancer Institute (NCI).[1] The structure of bryostatin 1 was determined in 1982.[10] As of 2010 20 different bryostatins had been isolated.[11]

The low concentration in bryozoans (to extract one gram of bryostatin, roughly one tonne of the raw bryozoans is needed) makes extraction unviable for large scale production. Due to the structural complexity, total synthesis has proved difficult, with only a few total syntheses reported so far. Total syntheses have been published for bryostatins 1, 2, 3, 7, 9 and 16.[12][13][14][15][16][17][18][19] Among them, Wender’s total synthesis of bryostatin 1 [19] is the shortest synthesis of any bryostatin reported, to date.

A number of structurally simpler synthetic analogs also have been prepared which exhibit similar biological profile and in some cases greater potency, which may provide a practical supply for clinical use.[20]

Biosynthesis
B. Neritina biosynthetic pathway for bryostatins.

In B. Neritina, bryostatin biosynthesis is carried out through a type I polyketide synthase cluster, bry. BryR is the secondary metabolism homolog of HMG-CoA synthase, which is the PKS in bacterial primary metabolism. In the bryostatin pathway, the BryR module catalyzes β-Branching between a local acetoacetyl acceptor acyl carrier protein (ACP-a) and an appropriate donor BryU acetyl-ACP (ACP-d).[21]

The first step involves the loading of a malonyl unit onto a discrete BryU ACP-d within an initial BryA module. The extended BryU product in BryA is then loaded onto a cysteine sidechain of BryR for interaction with ACP-a. Upon interaction, BryR then catalyzes β-Branching, facilitating an aldol reaction between the alpha-carbon of the BryU unit and the β-ketone of ACP-a, yielding a product similar to HMGS products in primary metabolism. After β-Branching, subsequent dehydration by a BryT enoyl-CoA hydratase homolog (ECH), as well as BryA O-methylation and BryB double bond isomerization of the generated HMGS product, are carried out in specific domains of the bry cluster. These post-β-Branching steps generate the vinyl methylester moieties which are found in all natural product bryostatins. Finally, BryC and BryD are responsible for further extension, pyran ring closure, and cyclization of the HMGS product to produce the novel bryostatin product.[22]

In the presence of BryR, ACP-d conversion to holo-ACP-d was observed prior to β-Branching. BryR was shown to have high specificity for ACP-d only after this conversion. Specificity for these protein-bound groups is a feature that differentiates the HMGS homologs found in primary metabolism, where HMGS typically acts on substrates linked to Coenzyme A, from those found in non-ribosomal peptide synthase (NRPS) or PKS pathways such as the bryostatin pathway.[21]

gollark: QUITE EASILY
gollark: You can borrow some of my turtles for 10KST/hour.
gollark: *IS HOLDING SHIFT RATHER THAN CAPSLOCK*(technically)
gollark: I just checked this, and it seems oddly active.
gollark: What's going on?

References
  1. Halford B (24 October 2011). "The Bryostatins' Tale". Chemical and Engineering News. 89 (43): 10–17. doi:10.1021/cen-v089n043.p010.
  2. Kollár P, Rajchard J, Balounová Z, Pazourek J (February 2014). "Marine natural products: bryostatins in preclinical and clinical studies". Pharmaceutical Biology. 52 (2): 237–42. doi:10.3109/13880209.2013.804100. PMID 24033119.
  3. name=Kollar2014rev>Kollár P, Rajchard J, Balounová Z, Pazourek J (February 2014). "Marine natural products: bryostatins in preclinical and clinical studies". Pharmaceutical Biology. 52 (2): 237–42. doi:10.3109/13880209.2013.804100. PMID 24033119.
  4. Trindade-Silva AE, Lim-Fong GE, Sharp KH, Haygood MG (December 2010). "Bryostatins: biological context and biotechnological prospects". Current Opinion in Biotechnology. 21 (6): 834–42. doi:10.1016/j.copbio.2010.09.018. PMC 4497553. PMID 20971628.
  5. Clinical trial number NCT00606164 for "Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics Study of Bryostatin 1 in Patients With Alzheimer's Disease" at ClinicalTrials.gov
  6. "Alzheimer's Researchers Discover Bryostatin Can Slow, Reverse Disease Progression". Alzheimer's News Today. 19 August 2014.
  7. Clinical trial number NCT02431468 for "A Study Assessing Bryostatin in the Treatment of Moderately Severe to Severe Alzheimer's Disease" at ClinicalTrials.gov
  8. Taylor NP (May 1, 2017). "Neurotrope misses primary endpoint in Alzheimer's trial". FierceBiotech.
  9. Nelson TJ, Sun MK, Lim C, Sen A, Khan T, Chirila FV, Alkon DL (2017). "Bryostatin Effects on Cognitive Function and PKCɛ in Alzheimer's Disease Phase IIa and Expanded Access Trials". Journal of Alzheimer's Disease. 58 (2): 521–535. doi:10.3233/JAD-170161. PMC 5438479. PMID 28482641.
  10. Pettit GR, Cherry Herald L, Doubek DL, Herald DL, Arnold E, Clardy J (1982). "Isolation and structure of bryostatin 1". J. Am. Chem. Soc. 104 (24): 6846–6848. doi:10.1021/ja00388a092.
  11. Hale KJ, Manaviazar S (April 2010). "New approaches to the total synthesis of the bryostatin antitumor macrolides". Chemistry: An Asian Journal. 5 (4): 704–54. doi:10.1002/asia.200900634. PMID 20354984.
  12. Keck GE, Poudel YB, Cummins TJ, Rudra A, Covel JA (February 2011). "Total synthesis of bryostatin 1". Journal of the American Chemical Society. 133 (4): 744–7. doi:10.1021/ja110198y. PMC 3030632. PMID 21175177.
  13. Evans DA, Carter PH, Carreira EM, Charette AB, Prunet JA, Lautens M (1999). "Total Synthesis of Bryostatin 2". J. Am. Chem. Soc. 121 (33): 7540–7552. doi:10.1021/ja990860j.
  14. Ohmori K, Ogawa Y, Obitsu T, Ishikawa Y, Nishiyama S, Yamamura S (July 2000). "Total Synthesis of Bryostatin". Angewandte Chemie. 39 (13): 2290–2294. doi:10.1002/1521-3773(20000703)39:13<2290::AID-ANIE2290>3.0.CO;2-6. PMID 10941067.
  15. Kageyama M, Tamura T, Nantz MH, Roberts JC, Somfai P, Whritenour DC, Masamune S (1990). "Synthesis of Bryostatin 7". J. Am. Chem. Soc. 112 (20): 7407–7408. doi:10.1021/ja00176a058.
  16. Lu Y, Woo SK, Krische MJ (September 2011). "Total synthesis of bryostatin 7 via C-C bond-forming hydrogenation". Journal of the American Chemical Society. 133 (35): 13876–9. doi:10.1021/ja205673e. PMC 3164899. PMID 21780806.
  17. Wender PA, Schrier AJ (June 2011). "Total synthesis of bryostatin 9". Journal of the American Chemical Society. 133 (24): 9228–31. doi:10.1021/ja203034k. PMC 3129979. PMID 21618969.
  18. Trost BM, Dong G (November 2008). "Total synthesis of bryostatin 16 using atom-economical and chemoselective approaches". Nature. 456 (7221): 485–8. Bibcode:2008Natur.456..485T. doi:10.1038/nature07543. PMC 2728752. PMID 19037312.
  19. Wender PA, Hardman CT, Ho S, Jeffreys MS, Maclaren JK, Quiroz RV, Ryckbosch SM, Shimizu AJ, Sloane JL, Stevens MC (October 2017). "Scalable synthesis of bryostatin 1 and analogs, adjuvant leads against latent HIV". Science. 358 (6360): 218–223. doi:10.1126/science.aan7969. PMC 5714505. PMID 29026042.
  20. Wender PA, Baryza JL, Bennett CE, Bi FC, Brenner SE, Clarke MO, Horan JC, Kan C, Lacôte E, Lippa B, Nell PG, Turner TM (November 2002). "The practical synthesis of a novel and highly potent analogue of bryostatin". Journal of the American Chemical Society. 124 (46): 13648–9. doi:10.1021/ja027509+. PMID 12431074.
  21. Buchholz TJ, Rath CM, Lopanik NB, Gardner NP, Håkansson K, Sherman DH (October 2010). "Polyketide β-branching in bryostatin biosynthesis: identification of surrogate acetyl-ACP donors for BryR, an HMG-ACP synthase". Chemistry & Biology. 17 (10): 1092–100. doi:10.1016/j.chembiol.2010.08.008. PMC 2990979. PMID 21035732.
  22. Slocum ST, Lowell AN, Tripathi AN, Shende VV, Smith JL, Sherman DH (2018). Chemoenzymatic Dissection of Polyketide β-Branching in the Bryostatin Pathway. Methods in Enzymology. 604. pp. 207–236. doi:10.1016/bs.mie.2018.01.034. ISBN 9780128139592. PMC 6327954. PMID 29779653.

Further reading
  • Proksch P, Edrada RA, Ebel R (July 2002). "Drugs from the seas - current status and microbiological implications". Applied Microbiology and Biotechnology. 59 (2–3): 125–34. doi:10.1007/s00253-002-1006-8. PMID 12111137.
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