- Methodology article
- Open Access
Building blocks for automated elucidation of metabolites: natural product-likeness for candidate ranking
BMC Bioinformatics volume 15, Article number: 234 (2014)
In metabolomics experiments, spectral fingerprints of metabolites with no known structural identity are detected routinely. Computer-assisted structure elucidation (CASE) has been used to determine the structural identities of unknown compounds. It is generally accepted that a single 1D NMR spectrum or mass spectrum is usually not sufficient to establish the identity of a hitherto unknown compound. When a suite of spectra from 1D and 2D NMR experiments supplemented with a molecular formula are available, the successful elucidation of the chemical structure for candidates with up to 30 heavy atoms has been reported previously by one of the authors. In high-throughput metabolomics, usually 1D NMR or mass spectrometry experiments alone are conducted for rapid analysis of samples. This method subsequently requires that the spectral patterns are analyzed automatically to quickly identify known and unknown structures. In this study, we investigated whether additional existing knowledge, such as the fact that the unknown compound is a natural product, can be used to improve the ranking of the correct structure in the result list after the structure elucidation process.
To identify unknowns using as little spectroscopic information as possible, we implemented an evolutionary algorithm-based CASE mechanism to elucidate candidates in a fully automated fashion, with input of the molecular formula and 13C NMR spectrum of the isolated compound. We also tested how filters like natural product-likeness, a measure that calculates the similarity of the compounds to known natural product space, might enhance the performance and quality of the structure elucidation. The evolutionary algorithm is implemented within the SENECA package for CASE reported previously, and is available for free download under artistic license at http://sourceforge.net/projects/seneca/. The natural product-likeness calculator is incorporated as a plugin within SENECA and is available as a GUI client and command-line executable. Significant improvements in candidate ranking were demonstrated for 41 small test molecules when the CASE system was supplemented by a natural product-likeness filter.
In spectroscopically underdetermined structure elucidation problems, natural product-likeness can contribute to a better ranking of the correct structure in the results list.
A significant number of the small molecules involved in the metabolism of organisms is still unknown. Methods for the structure elucidation of unknown metabolites are therefore needed. Computer-assisted structure elucidation (CASE), a field that has been researched for over 40 years , lends itself to this end. For complex structure elucidation problems, a rich set of mass spectral as well as 1D and 2D NMR spectroscopic information is required .
Under high-throughput conditions, however, only spectroscopic information that can be recorded quickly is used. Therefore, successful structure determination based on a limited set of spectroscopic information is important. 1D proton NMR is the most commonly used NMR method in metabolomics; however, in the present study, we based the structure elucidation on carbon-13 NMR because reliable open-source methods for proton prediction, including the coupling constants required to produce realistic 1D spectra, are not available. It is common knowledge that 1D NMR alone is usually not sufficient to establish the identity of a hitherto unknown compound.
Here, we investigated whether NP-likeness can be used as another component to the fitness evaluators to help elucidate candidates with minimum spectral information and increase the likelihood of a natural product ranking highly in a set of solutions. The methods presented here have been implemented in the SENECA system, an open-source java-based desktop application to perform CASE for organic molecules. The application takes a molecular formula generated from high-resolution mass spectrometry and spectral data from a suite of NMR experiments and performs a stochastic search in the constitutional space, guided by a fitness function. With the above input, the ability of the application to produce the correct structure for candidates with up to 30 heavy atoms has been demonstrated previously . Other systems have been shown to solve even larger problems, but these systems are closed-source and proprietary .
SENECA has been refactored completely and is now based on the Chemistry Development Kit (CDK), a popular open-source library for cheminformatics [7, 8]. The CDK contains a graph-based, object-oriented representation of molecules and provides flexible functionalities to perform various operation on molecules, including valence electrons check, ring perception, aromaticity detection, mutation, and atom environment representation. SENECA performs a stochastic search of constitution space (the space made up of all chemical compounds with the same gross formula), guided by a fitness or scoring function, which contains terms that evaluate the similarity of predicted and experimental spectra and terms that evaluate the validity of the currently inspected solution. SENECA contains implementations of simulated annealing  and an evolutionary algorithm. The latter is a completely new implementation and not related to the one reported previously  that was based on an older, obsolete library and that therefore was discontinued.
The latest version of SENECA is available both as a desktop application and as a command-line executable. SENECA is available for free download under artistic license from SourceForge .
Evolutionary algorithm for stochastic search
Evolutionary algorithms (EA) are based on the Darwinian principles of evolution, incorporating the concepts of natural selection and survival of the fittest. The overall scheme implemented by us for the optimization problem is similar to the scheme reported in , which has both mutation and recombination operators. In our scheme, we used only the mutation operator because it offered the desired results and was easier to configure. The simple EA scheme implemented by us is illustrated in Figure 1.
In our EA scheme, evolution starts with a population of a configurable number of randomly generated individuals, seeded by an initial molecular structure (connected graph) derived from the input molecular formula. To generate an initial population, the initial seed is mutated randomly by the mutation functionality within the CDK based on the Faulon mutation operator . Each individual is evaluated for fitness by our fitness evaluators and cross checked with termination conditions. The program can be configured to terminate if any of the following criteria are reached: maximum fitness, maximum allowed runtime, maximum allowed generations, or maximum allowed generations with no improvement. Here, we used only one of the termination conditions, namely the maximum allowed generations, because then we could collect all the isomers traversed and rank them to see if there was significant improvement in the ranking of the exact structure with the application of an NP-likeness filter. If the termination conditions are not met, each individual is mutated to generate one offspring, thereby doubling the population. The doubled population is evaluated again for fitness and the fittest individuals are chosen by round-robin tournament selection. If there is no improvement in fitness for five consecutive generations, fresh individuals are added to the population using a vicinity search around the top two fittest individuals. After the niche search the population is expanded from 16 to 24 and allowed to run for five generations. If again no fitness improvement is recorded, the population size is reduced back to 16 using tournament selection. The above evolution procedure is repeated until the termination conditions are met (default maximum allowed generations was set to 3000). Once met, the evolution is stopped and the elucidated candidates are reported.
A suite of fitness evaluators (judges), each of which evaluates a certain optimization criterion, e.g. agreement between the recorded chemical shift value from various NMR techniques (13C NMR, HHCOSY, HMBC, and HSQC) and the observed structural features in the candidate, has already been presented in SENECA [5, 9]. The scoring methods used by these judges are not described in detail here; however, the newly implemented fitness evaluators that have not been reported previously are discussed below.
NMRShiftDB is an open-access, open submission database that houses about 42,000 organic molecules and their associated recorded experimental 1D NMR spectra . The database can be accessed at http://nmrshiftdb.org.
The HOSE (Hierarchical Organisation of Spherical Environments) code  is a canonical way of capturing atom environments in a linear extendable fashion. A fitness evaluator from a previous version of SENECA  used the 651 one-sphere HOSE - 13C shift entries published by Bremser to keep the hybridization and heteroatom attachments of the predicted structures in check. The prediction precision can be improved if the extended environment of atoms can be captured by increasing the HOSE sphere height . The NMRShiftDB database is used to produce an index of HOSE with extended heights (from 1 to 4) and to associate it with a mean chemical shift and a confidence score, similar to Bremser’s approach .
The mean shift value for each HOSE code is calculated by averaging all the observed shifts over the molecule occurrence count. The standard deviation, therefore, will increase as the sphere height decreases. The confidence limit for each mean shift is calculated by multiplying the standard error with the two-sided Student’s t-distribution value for 95% confidence. If the confidence limit is less than 5 ppm, a minimum value of 5 ppm is assigned. The index generated serves as a lookup table for the new NMRShiftDBJudge.
The NMRShiftDB judge calculates the 13C spectrum for the candidate and assigns a fitness score based on its agreement with the experimental spectrum as shown in equation1. If the back-calculated (δ p r e d ) and the absolute deviation of a given experimental shift (δ e x p ) is within the confidence limit (CL) offered for that shift value, full points (P m a x ) are awarded for that carbon atom, otherwise zero. The summation of all the carbon atom scores gives the total score, validating the agreement between the 13C spectrum and the expected atom environments. Equation2 can be applied to normalize the score between 0 and 1.
With only NMRShiftDBJudge many isomers will emerge as the fittest by satisfying all the fragment-to-shift associations. This is a classic problem in CASE, i.e. the possibility of finding not one but many structural candidates that satisfy the given NMR constraints. Then expert opinion is relied on to pick the correct candidate solution. Hence, candidate ranking methods are indispensable in CASE when numerous solutions are given.
An automated way to rank these candidate solutions is to check their structural validity, for example by calculating their structural similarity with known NPs. Therefore, inclusion of a NPLikenessJudge is expected to improve the ranking of the candidates by penalizing improbable structures on the fly during evolution. To make decisions on the NP-likeness of a molecule, knowledge about the structural space of known NPs as opposed to synthetics is used. Previously, we reported such a scorer based on the open-data of known natural products and synthetics , with the main motivation of including it in the CASE program. We implemented a NPLikenessJudge by including the NP-likeness calculator within SENECA. The judge scores molecules for NP-likeness based on the occurrence of its fragments in the known natural product fragment space. The NP score given is between -3.5 and +3.5, where a higher score indicates greater NP-likeness. This score is normalized between 0 and 1 using equation3, where max and min are the most extreme values given by the NP-likeness scorer.
When NPLikenessJudge is used along with NMRShiftDBJudge the total cost is calculated using equation4. Thus, the candidate molecule is weighted more for NMR agreement and less for NP-likeness.
Another way to filter improbable structures during evolution is to check for structures that are sterically constrained. AntiBredtJudge penalizes a structure if it has a double bond at bridgehead atoms in rings with seven or less atoms. An algorithm to detect these unrealistic structures was reported previously  and this algorithm has been implemented in our CASE scheme.
Test case collection
To test the performance of the CASE system in predicting the correct structures using only the 13C spectrum, we collected 41 test cases from the Journal of Natural Products. We selected molecules with heavy atom counts ≤ 15 from recently published articles. From each article, the molecular formulae (MF), 13C chemical shifts, and DEPT 90 and DEPT 135 assignments were extracted to determine the number of hydrogen atoms attached to carbon atoms and then the published molecular structure was extracted for final cross validation. The MF and spectrum information were entered manually into the SENECA GUI client and saved as a SENECA markup language (SML) file, SENECA’s native file format based on XML. The molecular structure information was drawn using a structure drawer and saved as an MDL mol file to be used for identifying the correct structure in the solution set at the end of the CASE. All the structures were cross checked with the NMRShiftDB index to ensure that none of them were already present in the index. The collected test cases along with their NP-likeness score are illustrated in Figure 2.
Results and discussion
Performance of the CASE system
The performance of SENECA was tested using only the new fitness evaluators NMRShiftDBJudge, NPLikenessJudge, and AntiBredtJudge. To test the enhancement in candidate ranking with the application of NP-likeness, we performed two different evaluations for the 41 test cases. In the first evaluation (NMR_only), only two of the judges, NMRShiftDBJudge and AntiBredtJudge, were used, and in the second evaluation (NMR_NP) all three judges were used. The stochastic search does not guarantee that the global optimum will be found in one run; therefore, it is common to collect the results from several runs, and then combine and rank them. To test the performance of the CASE system, we performed 100 sequential runs for every test case, i.e. 4100 runs for each of the NMR_only and NMR_NP evaluations. Each run performs an evolution that terminates after 3000 generations and reports back all the elucidated candidates.
We observed that the frequency of elucidating the correct structure in the solution set was higher with the three NMR_NP judges than with the two NMR_only judges as shown in Figure 3. Although the retrieval percentage was low because of the spectroscopically underdetermined problems among the test cases, there was a 9.1% overall improvement in the predictions of correct candidates when NPLikenessJudge was included as a judge in the evaluations. Correct structures were retrieved in the solution set for 36 of the 41 cases with the application of all our fitness evaluators. The five cases for which no correct solution was found are numbered 2, 4, 22, 28, and 35 in Figure 2. The most interesting question is: in how many of the 36 retrieved cases was the correct candidate ranked the highest and how frequently did this happen? As illustrated in Figure 4, nine out of 34 cases and 17 out of 35 cases were ranked the highest using the NMR_only and NMR_NP judges, respectively, indicating that the application of NP-likeness frequently improved the rank of the correct solution. The improvement in ranking through the application of NPLikenessJudge is also indicated in Figure 5 and Figure 6, where the overall rank distribution is plotted for all test cases across all runs where there was a correct structure prediction. The empty indices in Figure 5 indicate that there was no correct prediction for these test cases in any of the 100 runs. Figure 6 using a violin plot summarises the distribution of overall ranks shown in Figure 5. The averaged-out rank distribution in Figure 7 shows how application of an NP-likeness filter tended to improve overall the rank of the correct solution among other predicted candidates.
Here, the application of natural product-likeness to achieve a higher ranking of the correct compound in automated structure elucidation of natural products with an otherwise limited set of spectroscopic information is presented. The newly developed methods described in this article are implemented in the open-source SENECA package for CASE, which features an evolutionary algorithm for structure elucidation and is available as a GUI client or as a stand-alone command-line executable. Fitness evaluators based on 13C NMR spectrum-to-structure associations in the NMRShiftDB database  and an NP-likeness score  have been integrated in the scoring function of the evolutionary algorithm scheme. With our publicly available open-data based fitness evaluators we have demonstrated the successful elucidation of correct structures for unknowns in 36 of 41 test cases, and achieved the highest rank for the correct structures of 17 of the 36 cases. We have also shown that significant improvement in overall prediction frequency and average ranking can be achieved with the application of the NP-likeness filter. We believe that these results can lead to improvements in CASE systems for use in metabolomics data analysis pipelines. The open-source, open-data implementation allows other researchers to contribute to or modify the package, and use their own training data for fitness evaluation.
Steinbeck C: The automation of natural product structure elucidation. Curr Opinion Drug Discov Dev. 2001, 4 (3): 338-342.
Steinbeck C: Computer-assisted structure elucidation. Handbook of Chemoinformatics. Edited by: Gasteiger J, Engel T. 2003, Weinheim: John Wiley & Sons, 1378-1406.
Peironcely JE, Reijmers T, Coulier L, Bender A, Hankemeier T: Understanding and classifying metabolite space and metabolite-likeness. PloS one. 2011, 6 (12): e28966-10.1371/journal.pone.0028966.
Jayaseelan K, Moreno P, Truszkowski A, Ertl P, Steinbeck C: Natural product-likeness score revisited: an open-source, open-data implementation. BMC Bioinformatics. 2012, 13: 106-10.1186/1471-2105-13-106.
Steinbeck C: SENECA: A platform-independent, distributed, and parallel system for computer-assisted structure elucidation in organic chemistry. J Chem Inf Comput Sci. 2001, 41 (6): 1500-1507. 10.1021/ci000407n.
Blinov KA, Carlson D, Elyashberg ME, Martin GE, Martirosian ER, Molodtsov S, Williams AJ: Computer-assisted structure elucidation of natural products with limited 2D NMR data: application of the StrucEluc system. Magn Reson Chem: MRC. 2003, 41 (5): 359-372. 10.1002/mrc.1187.
Steinbeck C, Han YQ, Kuhn S, Horlacher O, Luttmann E, Willighagen E: The Chemistry Development Kit (CDK): an open-source Java library for chemo- and bioinformatics. J Chem Inf Comput Sci. 2003, 43 (2): 493-500. 10.1021/ci025584y.
Steinbeck C, Hoppe C, Kuhn S, Guha R, Willighagen EL: Recent developments of the Chemistry Development Kit (CDK) - an open-source Java library for chemo- and bioinformatics. Curr Pharm Des. 2006, 12 (17): 2111-2120. 10.2174/138161206777585274.
Han Y, Steinbeck C: Evolutionary-algorithm-based strategy for computer-assisted structure elucidation. J Chem Inf Model. 2004, 44 (2): 489-498. 10.1021/ci034132y.
Jayaseelan KV, Steinbeck C: SENECA - Sourceforge availability. [http://sourceforge.net/projects/seneca/],
Faulon JL: Stochastic generator of chemical structure. 2. Using simulated annealing to search the space of constitutional isomers. J Chem Inf Comput Sci. 1997, 36: 731-740.
Steinbeck C, Kuhn S: NMRShiftDB - compound identification and structure elucidation support through a free community-built web database. Phytochemistry. 2004, 65 (19): 2711-2717. 10.1016/j.phytochem.2004.08.027.
Bremser W: HOSE - novel substructure code. Anal Chem Acta. 1977, 103: 355-365.
Bremser W: Expectation ranges of 13 C NMR chemical shifts. Magn Reson Chem. 1985, 23: 271-275. 10.1002/mrc.1260230413.
Nuzillard JM: Quick method for Anti-Bredt structure detection. J Chem Inf Comput Sci. 1994, 34: 723-724. 10.1021/ci00020a004.
KVJ thanks her colleagues from the Cheminformatics and Metabolism group at the European Bioinformatics Institute for their active support and critical comments. We especially thank Luis Filipe de Figueiredo for helping with the initial refactoring of SENECA and its upload to SourceForge. We thank the open-source communities of the Chemistry Development Kit. This work was supported by funds from the Biotechnology and Biological Sciences Research Council (BBSRC) [Grant number: BB/K004301/1].
The authors declare that they have no competing interests.
CS conceived the project and guided the development. KVJ conducted the study, selected the data, implemented the evolutionary algorithm scheme and new fitness evaluators within SENECA, and tested it. Both authors contributed to the manuscript draft, and read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Jayaseelan, K.V., Steinbeck, C. Building blocks for automated elucidation of metabolites: natural product-likeness for candidate ranking. BMC Bioinformatics 15, 234 (2014) doi:10.1186/1471-2105-15-234
- Computer-assisted structure elucidation
- Natural product-likeness