#METABOLOMICS WORKBENCH agoldman_20240429_061721 DATATRACK_ID:4798 STUDY_ID:ST003182 ANALYSIS_ID:AN005226 PROJECT_ID:PR001981
VERSION             	1
CREATED_ON             	April 30, 2024, 11:39 am
#PROJECT
PR:PROJECT_TITLE                 	METTL3-mediated chromatin contacts promote stress granule phase separation
PR:PROJECT_TITLE                 	through metabolic reprogramming during senescence
PR:PROJECT_SUMMARY               	METTL3 is the catalytic subunit of the methyltransferase complex, which mediates
PR:PROJECT_SUMMARY               	m6A modification to regulate gene expression. In addition, METTL3 regulates
PR:PROJECT_SUMMARY               	transcription in an enzymatic activity-independent manner by driving changes in
PR:PROJECT_SUMMARY               	high-order chromatin structure. However, how these functions of MTC are
PR:PROJECT_SUMMARY               	coordinated remains unknown. Here we show that the methyltransferase complex
PR:PROJECT_SUMMARY               	coordinates its enzymatic activity-dependent and independent functions to
PR:PROJECT_SUMMARY               	regulate cellular senescence, a state of stable cell growth arrest.
PR:PROJECT_SUMMARY               	Specifically, METTL3-mediated chromatin loops induce Hexokinase 2 expression
PR:PROJECT_SUMMARY               	through the three-dimensional chromatin organization during senescence. Elevated
PR:PROJECT_SUMMARY               	Hexokinase 2 expression subsequently promotes liquid-liquid phase separation,
PR:PROJECT_SUMMARY               	manifesting as stress granule phase separation, by driving metabolic
PR:PROJECT_SUMMARY               	reprogramming. This correlates with an impairment of translation of cell-cycle
PR:PROJECT_SUMMARY               	related mRNAs harboring polymethylated m6A sites. In summary, our results report
PR:PROJECT_SUMMARY               	a coordination of m6A-dependent and -independent function of the
PR:PROJECT_SUMMARY               	methyltransferase complex in regulating senescence through phase separation
PR:PROJECT_SUMMARY               	driven by metabolic reprogramming.
PR:INSTITUTE                     	University of Texas MD Anderson Cancer Center
PR:LAST_NAME                     	Zhang
PR:FIRST_NAME                    	Rugang
PR:ADDRESS                       	3SCR3.4121, 1901 East RD, Houston, TX, 77054
PR:EMAIL                         	rzhang11@mdanderson.org
PR:PHONE                         	832-748-6422
#STUDY
ST:STUDY_TITLE                   	METTL3-mediated chromatin contacts promote stress granule phase separation
ST:STUDY_TITLE                   	through metabolic reprogramming during senescence
ST:STUDY_SUMMARY                 	METTL3 is the catalytic subunit of the methyltransferase complex, which mediates
ST:STUDY_SUMMARY                 	m6A modification to regulate gene expression. In addition, METTL3 regulates
ST:STUDY_SUMMARY                 	transcription in an enzymatic activity-independent manner by driving changes in
ST:STUDY_SUMMARY                 	high-order chromatin structure. However, how these functions of MTC are
ST:STUDY_SUMMARY                 	coordinated remains unknown. Here we show that the methyltransferase complex
ST:STUDY_SUMMARY                 	coordinates its enzymatic activity-dependent and independent functions to
ST:STUDY_SUMMARY                 	regulate cellular senescence, a state of stable cell growth arrest.
ST:STUDY_SUMMARY                 	Specifically, METTL3-mediated chromatin loops induce Hexokinase 2 expression
ST:STUDY_SUMMARY                 	through the three-dimensional chromatin organization during senescence. Elevated
ST:STUDY_SUMMARY                 	Hexokinase 2 expression subsequently promotes liquid-liquid phase separation,
ST:STUDY_SUMMARY                 	manifesting as stress granule phase separation, by driving metabolic
ST:STUDY_SUMMARY                 	reprogramming. This correlates with an impairment of translation of cell-cycle
ST:STUDY_SUMMARY                 	related mRNAs harboring polymethylated m6A sites. In summary, our results report
ST:STUDY_SUMMARY                 	a coordination of m6A-dependent and -independent function of the
ST:STUDY_SUMMARY                 	methyltransferase complex in regulating senescence through phase separation
ST:STUDY_SUMMARY                 	driven by metabolic reprogramming.
ST:INSTITUTE                     	University of Texas MD Anderson Cancer Center
ST:LAST_NAME                     	Zhang
ST:FIRST_NAME                    	Rugang
ST:ADDRESS                       	3SCR3.4121, 1901 East RD, Houston, TX, 77054
ST:EMAIL                         	rzhang11@mdanderson.org
ST:PHONE                         	832-748-6422
#SUBJECT
SU:SUBJECT_TYPE                  	Cultured cells
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Pro_1	Treatment:Pro | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Pro_1-S4.raw
SUBJECT_SAMPLE_FACTORS           	-	Pro_2	Treatment:Pro | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Pro_2-S5.raw
SUBJECT_SAMPLE_FACTORS           	-	Pro_3	Treatment:Pro | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Pro_3-S6.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shctrl_1	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shctrl_1-S10.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shctrl_2	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shctrl_2-S11.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shctrl_3	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shctrl_3-S12.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_1	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_1-S16.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_2	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_2-S17.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_3	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_3-S18.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_MutHK2_1	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_MutHK2_1-S28.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_MutHK2_2	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_MutHK2_2-S29.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_MutHK2_3	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_MutHK2_3-S30.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_WTHK2_1	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_WTHK2_1-S22.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_WTHK2_2	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_WTHK2_2-S23.raw
SUBJECT_SAMPLE_FACTORS           	-	Sen_shHK2_WTHK2_3	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	RAW_FILE_NAME(raw_data)=Zhang_m22-L299_C13_Sen_shHK2_WTHK2_3-S24.raw
#COLLECTION
CO:COLLECTION_SUMMARY            	IMR90 primary human diploid lung embryonic fibroblasts were used and cultured in
CO:COLLECTION_SUMMARY            	DMEM medium supplemented with 10% fetal bovine serum (FBS), L-glutamine, sodium
CO:COLLECTION_SUMMARY            	pyruvate, non-essential amino acids, sodium bicarbonate and 1%
CO:COLLECTION_SUMMARY            	penicillin-streptomycin under low oxygen tension (2%).
CO:SAMPLE_TYPE                   	Cultured cells
#TREATMENT
TR:TREATMENT_SUMMARY             	Stable isotope tracer analysis using 13C6-glucose was conducted in three
TR:TREATMENT_SUMMARY             	biologically independent experiments for the following experimental groups:
TR:TREATMENT_SUMMARY             	control proliferating cells (Pro), RAS-induced senescent cells via 4-OHT with
TR:TREATMENT_SUMMARY             	control shRNA (Sen_shctrl), senescent cells with shRNA targeting HK2
TR:TREATMENT_SUMMARY             	(Sen_shHK2), senescent cells with shRNA targeting HK2 and rescued with wildtype
TR:TREATMENT_SUMMARY             	Flag-HK2 (Sen_shHK2_WTHK2), and senescent cells with shRNA targeting HK2 and
TR:TREATMENT_SUMMARY             	rescued with mutant Flag-HK2 (Sen_shHK2_MutHK2). The experiments were performed
TR:TREATMENT_SUMMARY             	by seeding cells at a density of 3 × 10^5 cells per 6 cm dish and incubating
TR:TREATMENT_SUMMARY             	them with 25 mM [13C6]-glucose tracer in glucose-free medium for 30 min.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Following incubation, the cells were washed with chilled PBS and incubated with
SP:SAMPLEPREP_SUMMARY            	500 µl of extraction solution (80:20 v/v methanol/water) at 4 °C for 5
SP:SAMPLEPREP_SUMMARY            	minutes. Next, cells were scraped with a polypropylene cell scraper and the
SP:SAMPLEPREP_SUMMARY            	extraction solution from each sample was collected, vortexed, and incubated on
SP:SAMPLEPREP_SUMMARY            	dry ice for at least 30 min. Then, each sample was centrifuged at maximum speed
SP:SAMPLEPREP_SUMMARY            	at 4 °C for 10 minutes, and the resulting supernatant was used for metabolic
SP:SAMPLEPREP_SUMMARY            	measurements.
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	Hydrophilic interaction liquid chromatography (HILIC) was performed at 0.2
CH:CHROMATOGRAPHY_SUMMARY        	ml/min on a ZIC-pHILIC column (2.1 mm × 150 mm, 5 µm particle size, EMD
CH:CHROMATOGRAPHY_SUMMARY        	Millipore) at 45 °C. Solvent A was 20 mM ammonium carbonate, 0.1% ammonium
CH:CHROMATOGRAPHY_SUMMARY        	hydroxide, pH 9.2, and solvent B was acetonitrile. The gradient was 85% B for 2
CH:CHROMATOGRAPHY_SUMMARY        	min, 85% B to 20% B over 15 min, 20% B to 85% B over 0.1 min, and 85% B for 8.9
CH:CHROMATOGRAPHY_SUMMARY        	min. The autosampler was held at 4 °C. For each analysis, 4 µl of sample was
CH:CHROMATOGRAPHY_SUMMARY        	injected.
CH:CHROMATOGRAPHY_TYPE           	HILIC
CH:INSTRUMENT_NAME               	Thermo Vanquish Horizon UHPLC
CH:COLUMN_NAME                   	Merck SeQuant ZIC-pHILIC (150 x 2.1mm,5um)
CH:SOLVENT_A                     	100% water; 20 mM ammonium carbonate; 5 µM medronic acid; 0.1% ammonium
CH:SOLVENT_A                     	hydroxide
CH:SOLVENT_B                     	100% acetonitrile
CH:FLOW_GRADIENT                 	85% B for 2 min, 85% B to 20% B over 15 min, 20% B to 85% B over 0.1 min, and
CH:FLOW_GRADIENT                 	85% B for 8.9 min
CH:FLOW_RATE                     	0.2 ml/min
CH:COLUMN_TEMPERATURE            	45
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Thermo Q Exactive HF-X Orbitrap
MS:INSTRUMENT_TYPE               	Orbitrap
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	UNSPECIFIED
MS:MS_COMMENTS                   	The following parameters were used for the MS analysis: sheath gas flow rate,
MS:MS_COMMENTS                   	40; auxiliary gas flow rate, 10; sweep gas flow rate, 2; auxiliary gas heater
MS:MS_COMMENTS                   	temperature, 350 °C; spray voltage, 3.5 kV for positive mode and 3.2 kV for
MS:MS_COMMENTS                   	negative mode; capillary temperature, 325 °C; and funnel RF level, 40. All
MS:MS_COMMENTS                   	samples were analyzed by full MS with polarity switching. Technical injections
MS:MS_COMMENTS                   	of an unlabeled sample pool were analyzed throughout the sample sequence. The
MS:MS_COMMENTS                   	unlabeled sample pool was also analyzed by data-dependent MS/MS with separate
MS:MS_COMMENTS                   	runs for positive and negative ion modes. Full MS scans were acquired at 120,000
MS:MS_COMMENTS                   	resolution with a scan range of 65-975 m/z. Data-dependent MS/MS scans were
MS:MS_COMMENTS                   	acquired for the top 10 highest intensity ions at 15,000 resolution with an
MS:MS_COMMENTS                   	isolation width of 1.0 m/z and stepped normalized collision energy of 20-40-60.
MS:MS_COMMENTS                   	Annotation and quantitation of metabolites and carbon isotopologues with natural
MS:MS_COMMENTS                   	isotope abundance correction were performed using Compound Discoverer 3.3
MS:MS_COMMENTS                   	software (Thermo Scientific). Metabolite measurements were normalized based on
MS:MS_COMMENTS                   	the protein concentration in the protein pellets.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	Peak Area
MS_METABOLITE_DATA_START
Samples	Pro_1	Pro_2	Pro_3	Sen_shctrl_1	Sen_shctrl_2	Sen_shctrl_3	Sen_shHK2_1	Sen_shHK2_2	Sen_shHK2_3	Sen_shHK2_WTHK2_1	Sen_shHK2_WTHK2_2	Sen_shHK2_WTHK2_3	Sen_shHK2_MutHK2_1	Sen_shHK2_MutHK2_2	Sen_shHK2_MutHK2_3
Factors	Treatment:Pro | Sample source:lung embryonic fibroblasts	Treatment:Pro | Sample source:lung embryonic fibroblasts	Treatment:Pro | Sample source:lung embryonic fibroblasts	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	Treatment:Sen_shctrl | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_WTHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts	Treatment:Sen_shHK2_MutHK2 | Sample source:lung embryonic fibroblasts
AMP M+0	103793851.2	88596725.41	116556852.8	22540389.44	18513530.99	15425235.93	59077216.67	44547074.96	25744605.32	20267922.52	20761915.4	14014033.4	49456270.65	54673121.49	35875769.55
AMP M+1	0	0	0	0	0	0	0	0	0	0	0	12794.0613	0	0	0
AMP M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
AMP M+3	42309.9174	0	98583.43082	0	0	0	42264.38084	0	0	17678.58843	0	0	0	0	0
AMP M+4	152763.1229	0	0	0	0	0	22626.72751	0	0	0	0	0	0	0	0
AMP M+5	6198420.242	5148233.732	7444568.757	1543652.829	1155306.142	951633.7072	2191537.353	1461186.156	683017.6103	924726.1375	1002994.159	628972.8732	2175121.724	2178905.226	1383034.862
AMP M+6	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
AMP M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
AMP M+8	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
AMP M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
AMP M+10	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ADP M+0	102542588.3	83493331.45	87090774.85	55225875.51	44524051.39	33836081.79	114078880.2	131281362.5	79335440.71	53063303.96	61394976.39	40859321.4	81519453.8	96164920.45	62010155.79
ADP M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ADP M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ADP M+3	296341.1094	228846.9658	167343.4405	269471.0315	186565.7538	161876.634	229659.1777	234974.8276	116452.5481	401742.6352	461994.1629	236875.8474	226722.2428	202740.2479	143373.7973
ADP M+4	552504.8202	341456.982	464285.3915	128928.8035	176914.0537	123738.4141	124920.9173	235587.9403	208654.6353	247306.3452	162029.8277	184143.7103	250639.3208	266139.3152	183140.1178
ADP M+5	5977200.099	4713330.682	5366573.703	4696820.568	3317551.688	2348668.321	4293973.162	5134868.917	3052694.995	3265384.341	3522209.04	2522860.791	3358210.374	3712202.625	2458990.534
ADP M+6	0	0	0	1093.045937	3524.331493	0	0	0	0	0	0	0	0	0	0
ADP M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ADP M+8	0	0	0	0	0	0	71383.17642	0	0	0	0	0	0	0	0
ADP M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ADP M+10	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Ribose-5-phosphate M+0	809875.9885	705567.0434	682873.6836	1321420.87	889312.5105	1523557.778	1472218.231	3379249.72	2603064.779	3659826.47	2183726.54	1689977.668	2263751.76	3303811.162	2496803.919
Ribose-5-phosphate M+1	0	0	0	0	31102.70667	39154.68282	0	0	0	102282.6855	9636.692402	42707.25363	0	0	0
Ribose-5-phosphate M+2	2217279.233	2075156.434	2268830.064	3275502.945	2283809.446	3316039.067	2487117.059	3965922.193	3209733.742	4054153.094	3159797.481	2941056.821	3946129.797	6258526.758	4979428.469
Ribose-5-phosphate M+3	1780246.529	1604019.69	1811458.893	3582832.988	2521097.557	3753624.066	1571382.345	3256192.495	3216950.263	4414710.827	3372212.655	2683083.498	3136538.827	4785907.111	3603059.358
Ribose-5-phosphate M+4	0	0	0	375623.681	182280.4931	618994.7562	574370.2637	323191.0377	411124.9172	840052.073	498495.9853	348622.9456	456450.8578	901644.0857	822570.9392
Ribose-5-phosphate M+5	61050510.27	53449955.01	51416870.98	38743909.96	31998700.41	35173197.16	64598852.17	90789332.16	58795482.48	58573489.36	48968899.65	40028962.73	83009909.25	98701839.6	71706534.01
Fructose-1,6-bisphosphate M+0	16180904.43	10579048.9	17597032.73	19450676.97	7750397.419	12296228.35	8230390.028	16881282.39	9472580.212	10658221.38	22026218.28	13944047.48	15812148.28	19970955.93	13743637.71
Fructose-1,6-bisphosphate M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Fructose-1,6-bisphosphate M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Fructose-1,6-bisphosphate M+3	12014315.56	14373039.71	17865011.4	16663182.19	12448365.69	11842716.82	15501292.76	20178181.21	17901570.03	13097597.54	14050882.03	8985012.527	18846360.84	27111657.7	21526459.81
Fructose-1,6-bisphosphate M+4	0	92337.93396	0	173295.7935	221615.8894	232689.6261	304525.5155	0	196789.1837	245484.3887	196176.0973	126892.5082	200671.0712	8239.842235	93047.09168
Fructose-1,6-bisphosphate M+5	418783.3633	0	2126809.319	0	261795.3973	0	2472897.163	945456.2621	1050460.128	0	460311.5853	786990.167	436912.3502	0	921045.706
Fructose-1,6-bisphosphate M+6	263103116.9	231353070	231892194.5	104064384.3	86647908.42	72346705.35	238006164	278113317	193270988.7	114695102.9	116333163.5	73985574.77	216386895.9	245413031.3	170059657.2
Glucose-6-phosphate M+0	1145202.565	889954.3844	893480.2102	694697.9387	526701.0551	610087.4828	1123142.768	2033740.997	1606947.209	1321996.815	1507613.501	881386.0075	1572711.999	1636961.534	1327183.762
Glucose-6-phosphate M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Glucose-6-phosphate M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Glucose-6-phosphate M+3	0	0	0	0	0	0	29558.46935	0	146452.2086	0	0	0	0	0	0
Glucose-6-phosphate M+4	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Glucose-6-phosphate M+5	253.9248969	21870.407	0	0	0	0	17087.99061	0	4868.439955	0	0	67906.97056	0	0	0
Glucose-6-phosphate M+6	7241137.099	5118061.369	5757361.194	2087051.216	1792623.969	2004861.271	10410019.35	14859016.78	10117495.71	3737467.717	5281852.859	2680914.264	8404471.32	8337469.599	7330243.734
Adenosine M+0	76724845.08	52094434.22	56973005.33	47885041.74	30499970.3	30305905.74	119440500.3	154093307	89098245.8	78704781.9	74905253.06	39192802.77	113195609.1	122183503	100572052.7
Adenosine M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+3	0	0	55320.99747	0	0	0	330794.9897	202235.2431	77395.82892	435314.8882	191257.7852	103367.6747	171396.7942	173571.8741	167339.5474
Adenosine M+4	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+5	3792918.43	2287895.247	3098010.724	2703396.087	1440554.938	1636820.855	3800303.519	5200910.609	2460050.513	4172115.227	3417750.105	1722776.569	4267812.177	4448293.837	3679564.671
Adenosine M+6	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+8	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Adenosine M+10	0	4531.273943	0	0	0	0	4899.506161	4417.320405	1499.580077	0	0	0	2525.963205	2273.19432	1556.615202
ATP M+0	59335545.47	54305123.27	48157330.52	81393050.39	61392202.06	43303267.3	173409888.3	182609281.5	124737435	53545144.17	82068706.3	45489552.39	75849355.3	85283284.22	58221327.58
ATP M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+3	0	0	0	259819.7715	87544.94944	2378.435709	191467.7598	0	176937.5669	182250.9165	583647.9772	202382.8718	0	64654.01831	0
ATP M+4	0	0	0	0	38712.30808	0	59801.10914	0	12087.44699	0	0	0	0	0	0
ATP M+5	3185937.859	2622896.965	2822477.038	6591287.074	4264682.328	3124950.529	5581257.986	6422162.05	4318659.439	3573780.618	4875397.595	2854832.784	2950748.82	3119150.84	2270418.545
ATP M+6	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+8	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
ATP M+10	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+0	252750830.3	268477336.3	273129441.5	157620959.1	120119663.7	134993422.9	248495719.5	365708193.9	325368803.6	79821414.77	86647989.86	54450299.63	281562897.4	396146279.6	328331706.8
Inosine M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+2	0	0	0	0	0	203160.4577	0	0	0	0	234238.3045	0	0	0	0
Inosine M+3	496508.6759	182134.5012	371948.1166	1523141.976	1183550.521	1539200.157	850096.0822	625807.9549	1076035.896	1139153.138	586374.3339	694471.8697	602052.1287	1796227.575	1203779.314
Inosine M+4	0	0	128812.4057	0	0	0	12163.9132	0	156411.414	372020.7961	315297.1304	0	0	42536.46097	566199.4358
Inosine M+5	25088358.01	23407274.47	27000385.88	34470883.58	27000893.45	29397959.92	18777423.99	29191366.73	25381513.31	17494005.62	17822621.18	12693868.73	26600632.67	36759211.08	32539945.6
Inosine M+6	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+8	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
Inosine M+10	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+0	31043350.52	27493621.53	28371445.51	4249488.008	3914046.031	3377491.819	23458505.71	27836383.22	17550291.28	2383759.416	2217969.458	1723486.647	17444282.17	24831591.4	17726451.67
IMP M+1	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+2	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+3	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+4	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+5	2379937.654	1796628.342	2429529.255	459699.1948	364477.318	314128.3811	1077737.016	1587553.353	1065286.227	471461.9034	295585.5103	248897.4523	1114230.272	1572894.198	1183226.684
IMP M+6	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+7	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+8	0	0	180308.0595	0	0	0	434887.9736	473251.8367	298706.8704	0	0	0	721451.0962	408642.8851	601278.5799
IMP M+9	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
IMP M+10	0	0	0	0	0	0	0	0	0	0	0	0	0	0	0
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	RT
AMP M+0	8.795
AMP M+1	8.795
AMP M+2	8.795
AMP M+3	8.795
AMP M+4	8.795
AMP M+5	8.795
AMP M+6	8.795
AMP M+7	8.795
AMP M+8	8.795
AMP M+9	8.795
AMP M+10	8.795
ADP M+0	9.87
ADP M+1	9.87
ADP M+2	9.87
ADP M+3	9.87
ADP M+4	9.87
ADP M+5	9.87
ADP M+6	9.87
ADP M+7	9.87
ADP M+8	9.87
ADP M+9	9.87
ADP M+10	9.87
Ribose-5-phosphate M+0	9.887
Ribose-5-phosphate M+1	9.887
Ribose-5-phosphate M+2	9.887
Ribose-5-phosphate M+3	9.887
Ribose-5-phosphate M+4	9.887
Ribose-5-phosphate M+5	9.887
Fructose-1,6-bisphosphate M+0	11.613
Fructose-1,6-bisphosphate M+1	11.613
Fructose-1,6-bisphosphate M+2	11.613
Fructose-1,6-bisphosphate M+3	11.613
Fructose-1,6-bisphosphate M+4	11.613
Fructose-1,6-bisphosphate M+5	11.613
Fructose-1,6-bisphosphate M+6	11.613
Glucose-6-phosphate M+0	10.702
Glucose-6-phosphate M+1	10.702
Glucose-6-phosphate M+2	10.702
Glucose-6-phosphate M+3	10.702
Glucose-6-phosphate M+4	10.702
Glucose-6-phosphate M+5	10.702
Glucose-6-phosphate M+6	10.702
Adenosine M+0	4.159
Adenosine M+1	4.159
Adenosine M+2	4.159
Adenosine M+3	4.159
Adenosine M+4	4.159
Adenosine M+5	4.159
Adenosine M+6	4.159
Adenosine M+7	4.159
Adenosine M+8	4.159
Adenosine M+9	4.159
Adenosine M+10	4.159
ATP M+0	10.636
ATP M+1	10.636
ATP M+2	10.636
ATP M+3	10.636
ATP M+4	10.636
ATP M+5	10.636
ATP M+6	10.636
ATP M+7	10.636
ATP M+8	10.636
ATP M+9	10.636
ATP M+10	10.636
Inosine M+0	6.377
Inosine M+1	6.377
Inosine M+2	6.377
Inosine M+3	6.377
Inosine M+4	6.377
Inosine M+5	6.377
Inosine M+6	6.377
Inosine M+7	6.377
Inosine M+8	6.377
Inosine M+9	6.377
Inosine M+10	6.377
IMP M+0	9.88
IMP M+1	9.88
IMP M+2	9.88
IMP M+3	9.88
IMP M+4	9.88
IMP M+5	9.88
IMP M+6	9.88
IMP M+7	9.88
IMP M+8	9.88
IMP M+9	9.88
IMP M+10	9.88
METABOLITES_END
#END