;hsqc_fb.ref, avance500 07/15/02 #include "Gradaph.incl" #include "Avance.incl" ;1 hn, 15n edited noesy to water protons ;history ;written by sg 2/23/93 ;put in water flip_back 6/1/93 ;change to waternh 7/29/93 ;change to hnhsqc.dif 6/27/95 ;change to hsqcg.dat 10/7/95 ;changed to hsqc_fb.yt for DMX500 6/3/96 ;copied from hsqc_fb.dat_r ;Updated and checked 2/7/97 mam ;uthsasa avance500, 7/15/02, aph ;Adjust these as appropriate by commenting in/out #define FLIP_BACK #define CARBON_LABEL #define WATER_GATE ;Proton settings - Set carrier to H2O (ca 4.7 ppm) ;p1 - square 90 1H @ pl1, for excitation, typically p1 = 8.9u @ pl1 = -2dB ;p2 - square 90 1H @ pl1, for watergate, typically p2 = 1000u @ pl2 = +39.0dB ;p3 - shaped 90 1H @ sp0, for water flipback, typically p3 = 2m @ sp0 = +38.5 ; "spnam0 seduce1.jc", "spoffs0 0" ;Nitrogen settings - Set carrier to amide center (ca. 118 ppm) ;p7 - square 90 15N @ pl7, for excitation, typically p7 = 45u @ pl1 = -3.1dB ;pcpd3 - square 90 15N @ pl3, for cpd, typically pcpd3 = 200u @ pl3 = +10.0 ;The following is only necessary if CARBON_LABEL is defined ;13C pulses - carrier is set according to fqlist1 frequency list ; chose/edit in ased, should have two values, ; first is CA (56 ppm), second is CO (176 ppm) ;p5 - square 90 13C @ pl5, for excitation, p5 must equal 28.7u, typically pl5 = +2.6 ;in0=1/(2sw) nitrogen spectral window ;L3 nitrogen t1 points ;Gradient settings ;Note1 - grad times are preset, you do not need to adjust these ;Note2 - set grad params according to table below, note integer in first ;column is substituted to yield the parameter that is to be adjusted ;example for grad# 0, set "gpnam0 sine.32", "gpx0 20", "gpy0 0", "gpz0 -40" ; ;grad# gpnam# gpx# gpy# gpz# ;0 sine.32 20 0 -40 ;1 sine.32 20 0 40 ;Other Adjustments ;d1 - recycle time, typically d1 = 1s ;Optional Adjustments ;phcor14 - phase adjustment for p2@pl2 vs p1@pl1, typically +/- 1 degree ;phcor18 - phase adjustment for p2@pl2 vs p1@pl1, typically +/- 1 degree ;phcor13 - phase adjustment for p3@sp0 vs p1@pl1, typically +/- 1 degree ;PRESET DELAYS - DO NOT ADJUST ANYTHING BELOW THIS POINT ; "p15=2.5m" "p16=2.0m" "p17=0.4m" ; #ifdef CARBON_LABEL "d0=in0*0.5 - p7*0.637 -4u -p5*2.0" #else "d0=in0*0.5 - p7*0.637 - 2*p1" #endif ; "d4=2.5m" ;1/4Jhn - use 2.25m for larger proteins "d11=5m" "d12=1m" "d26=p7-p1" "d27=p5-p1" define delay pd2 "pd2=p2" define delay pd3 "pd3=p3" #define ON #undef OFF 1 ze 2 d11 BLKGRAD 1m d12 3 d12*3.0 4 d11 do:f3 10u pl1:f1 10u pl7:f3 10u pl5:f2 #ifdef ON #ifdef CARBON_LABEL 10u pl5:f2 10u fq1:f2 ;jump to 56ppm #endif ;***** presaturation ***** d1 1m UNBLKGRAD ;***** INEPT from proton to nitrogen antiphase ***** (p1 ph0):f1 d4 (p7*2 ph6):f3 (d26 p1*2 ph4):f1 d4 (p1 ph6):f1 6u pl2:f1 #ifdef FLIP_BACK (p2 ph18:r):f1 2u #else pd2 2u #endif p15:gp0 1.5m pl1:f1 ;***** nitrogen evolution period ***** (p7 ph3):f3 d0 #ifdef CARBON_LABEL 2u (p5*2 ph10):f2 (d27 p1*2 ph0):f1 2u fq1:f2 ;jump to 177ppm 4u (p5*2 ph10):f2 #else (p1*2 ph0):f1 ;proton refocusing #endif d0 (p7 ph7):f3 2u p16:gp0 1m #ifdef FLIP_BACK 10u (p3:sp0 ph13:r):f1 #else 5u pd3 #endif 10u 12u pl1:f1 (p1 ph0):f1 #ifdef WATER_GATE p17:gp1 950u pl2:f1 (p2 ph14:r):f1 2u pl1:f1 5u (p1*2 ph15):f1 2u pl2:f1 5u (p7*2 ph10):f3 (p2 ph14:r):f1 2u p17:gp1 #else 400u pl1:f1 950u pd2 (p7*2 ph10):f3 (d26 p1*2 ph15) pd2 400u #endif (2u ph0) 948u pl3:f3 ;996u for better ph1 for DMX500 5u #endif go=2 ph31 cpds3:f3 1m BLKGRAD d11 do:f2 do:f3 wr #0 if #0 zd d12 ip3 ;States-TPPI in nitrogen lo to 3 times 2 d12 id0 d12 ip31 d12 ip31 lo to 4 times l3 ;loop over nitrogen t1 points d12 do:f2 d12 do:f3 exit ph0=0 ph1=0 ph3=0 2 0 2 2 0 2 0 ph4=1 ph6=1 ph7=0 ph10=0 ph13=2 ;adjust using phcor13 ph14=2 2 0 0 ;adjust using phcor14 ph15=0 0 2 2 ph18=0 ;adjust using phcor18 ph31=0 2 0 2 2 0 2 0