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Melody discrimination and protein fold classification

Bywater, Robert,Middleton, Jonathan

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Melody disc imina ion and p o ein old classi ica ion Robe P. Bywa e a , Jona han N. Middle on b,c, * a F ancis C ick Ins i u e, London NW1 1AT, UK b Depa men o Music, Eas e n Washing on Uni e si y, Cheney, WA 99004, USA c School o In o ma ion Sciences, Uni e si y o Tampe e, 33041, Finland * Co esponding au ho . E-mail add ess: [email p o ec ed] (J.N. Middle on). Abs ac One o he g ea es challenges in heo e ical biophysics and bioin o ma ics is he iden i ica ion o p o ein olds om sequence da a. This can be ega ded as a pa e n ecogni ion p oblem. In his pape we epo he use o a melody gene a ion so wa e whe e he inpu s a e de i ed om calcula ions o e olu iona y in o ma ion, seconda y s uc u e, lexibili y, hyd opa hy and sol en accessibili y om mul iple sequence alignmen da a. The melodies so gene a ed a e de i ed om he sequence, and by in e ence, o he old, in ways ha gi e each old a sound ep esen a ion ha may acili a e analysis, ecogni ion, o compa ison wi h o he sequences. Keywo d: Bioin o ma ics 1. In oduc ion Globula p o eins a e linea copolyme s o amino acid esidues ha ha e s e ches o mo e o less egula geome y which a e packed oge he in ways ha a i s sigh appea any hing bu sys ema ic. The locally egula egions, called seconda y s uc u es, a e ei he helical (α-o 3 10 helix ype) o β-s ands, which can a ange hemsel es in ei he a mu ually pa allel o an ipa allel ashion o o m so-called β-shee s. Each amino acid esidue ype has a di e en p opensi y o a ou one o o he o hese s uc u al a angemen s [1,2,3,4]. The old ha ensues is likewise dependen on ano he p ope y o he amino acids, he hyd opa hy, o deg ee o Recei ed: 18 July 2016 Re ised: 4 Sep embe 2016 Accep ed: 30 Sep embe 2016 Heliyon 2 (2016) e00175 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). which he side chain o he esidue seeks o a oids con ac wi h he sol en wa e . This in u n a ec s he deg ee o which a gi en esidue will be bu ied in he in e io o lie on he su ace. These a e h ee o he majo a ibu es o polypep ide sequences ha con i e o de e mine he inal 3-dimensional (3D) s uc u e, and all h ee can be de e mined by p esen -day bioin o ma ics me hodology (see Me hods). One mo e complica ion ha needs o be deal wi h is he ac ha he polypep ides hemsel es may old in o mo e han one “independen ly olding uni ” along he chain. These uni s a e e e ed o as domains. Fo small p o eins he e is ypically only a single domain, bu la ge p o eins may ha e wo o mo e. These can be simila in cha ac e (and as such may be he esul o a gene duplica ion e en ) o di e en , depending on he unc ional needs o he p o ein. The assembly p ocess, which is well unde s ood a he le el o molecula biology, enlis s a ca aly ic p ocess e e ed o as splicing. This in ol es selec ing disjoin sec ions om he o iginal DNA sequence (genome) o ansla ion in o he “language”o p o eins whe ea e he splicing p ocess akes place in a de ined o de . P o ein olds, o mo e co ec ly, domain olds, can be classi ied in one o se e al ways [5, 6,7]. Wi h his as a backg ound o he pa e n ecogni ion p oblem, we now desc ibe he app oach we a e aking owa ds i s solu ion. He e, we explo e he use o melodic soni ica ion o disce n pa e ns o da a ha a e based on ce ain ea u es associa ed wi h p o ein s uc u es: e olu iona y in o ma ion, chemical p opensi ies and physical a ibu es. We an icipa e ha he pe cep ion o p o ein da a ia sonic ep esen a ion can assis esea che s in he p ocess o pa e n ecogni ion and s uc u al unde s anding. Melodic pa e ns o sound can become ools o assis p o ein chemis s in assigning old ypes o a gi en p o ein wi h a known sequence, bu unknown 3D s uc u e. The po en ial bene i s o using audi o y display o scien i ic da a as a means o de i e analy ical meaning ha e been o mally demons a ed since 1994 [8,9,10]. These au ho s a gued ha he human audi o y sys em has he sophis ica ion and he abili y o in e p e sounds “using mul iple laye s o unde s anding”[10].In e e ence o he choice o analy ical lis ening o e isual e iew o da a, sugges ions ha e been made [11] o he e ec ha “pa e ns may eme ge which a e o he wise unde ec able”. Al hough he analy ical and in e p e a i e p ocesses ( h ough lis ening) a e no comple ely unde s ood, he pe cep ual ap i udes ha e ecognized me i s: da a- o-sound pa ame e mappings and applica ions now se e many disciplines such as “chaos heo y, bio-medicine, in e aces o isually disabled people, da a mining, and seismology”[10]. Mo e speci ically o genome science, we an icipa e ha soni ica ions could highligh pa e ns o ind mu an s and gene ic disease ma ke s o which a ich collec ion o sequence da a is a ailable. A icle No~e00175 2h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). While mos da a a e obse ed, soni ica ions ha a e designed speci ically o cohe en da a- o-sound ep esen a ion can complemen mo e adi ional isual displays o da a and o e a use ul seconda y pe cep ualiza ion o analyze da a se s. In his pape we seek o c ea e soni ica ions o p o ein s uc u es ha can uniquely enhance ou abili y o ecognize pa e ns ela ed o p o ein olds. We ha e chosen pi ch as he mos basic and p ima y soni ica ion elemen o ep esen da a; hence he da a se s a e con e ed in o sequences o pi ches. The con e sion esul s a e melodic in na u e, demons a ing a simple and s aigh o wa d con e sion o clea ly pe cei e he soni ied da a pa e ns. O he sound elemen s such as ha mony and coun e poin wi h imb al a ie y did no yield simple lis ening en i onmen s o sequen ial da a pa e n ecogni ion. In some cases hy hmic mapping was applied as a seconda y soni ica ion pa ame e o enhance he melodies. The p esen s udy con ibu es o a ela i ely small collec ion o p e iously explo ed soni ica ions o p o ein s uc u es. In many cases, p e ious s udies sough o educa e and inspi e eade s wi h in e disciplina y connec ions be ween music and science, and making science mo e widely accessible. E o s, such as he Li e Music p ojec , we e designed o dual pu poses o c ea ing new pe cep ual models o p o ein analysis and enhancing elec o-acous ic music composi ions [12,13, 14,15]. In each soni ica ion s udy o p o eins, he p ojec s ha e u ilized hei own se o mapping sys ems o con e da a- o-music. As an example, he Li e Music p ojec [12] mapped p o ein esidues o pi ches ia hyd opa hy scales, a concep ha is simila o one o he mapping sys ems explained la e in his pape (wi h esul s ha a e qui e di e en ). In he Takahashi and Mille pilo s udy [13] amino acids we e assigned o disc e e pi ches, and hen o cho ds and hy hm o make he esul s mo e musical. 2. Me hods 2.1. Da a p epa a ion om p o ein sequence da abases The soni ica ion s udy epo ed a his ime is ea u ing h ee p o eins, each ep esen ing h ee SCOP [5] classes, α-helix ype, p o eins composed o β-s ands, and mixed α/β ype. α-helix: 1ny9.pdb (MW 10.60 kD, α-helix 73.4%, 3 10 -helix 3.2%, β-s and 0.0%, u n 10.6%, coil 12.8%) β-shee : 1 75.pdb (MW 7.85 kD, α-helix 0.0%, 3 10 -helix 0.0%, β-s and 23.5%, u n 26.5%, coil 50.0%) α/β ype: 4ake.pdb (MW 23.59 kD, α-helix 43.5%, 3 10 -helix 5.1%, β-s and 15.4%, u n 20.6%, coil 15.4%) A icle No~e00175 3h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). In p epa a ion o ou o e all s udy, we o iginally chose p o eins iden ical o ep esen a i es o hese domain old classes s udied in a ecen publica ion [16] ha had as i s aim he in es iga ion o domain old space. The p o eins chosen we e 1ny9, 1 75, and 1di .pdb (MW 16.31 kD, α-helix 32.2%, 3 10 -helix 6.0%, β-s and 30.9%, u n 13.4%, coil 17.4%). Since hese p o eins a e ela i ely small (sequence leng h, MW), a ou h p o ein, 4ake, was added o he s udy. Like 1di , 4ake is a α/β ype, bu much la ge . Fu he , o he p esen s udy, we decided o exclude 1di in lieu o 4ake, al hough he 1di p o ein ea u es in an ex ension o his wo k, which is al eady unde way. The eason o excluding his p o ein a his s age has o do wi h he s uc u al pa ame e s chosen o he i s pa o his wo k (see below). In he case o 1ny9, his is an NMR s uc u e con aining 10 al e na i e solu ions o he s uc u e. The bes consensus s uc u e, no. 8, was de e mined using he WHAT IF p og am [17]. The selec ed s uc u e he ein simply called 1ny9 is, s ic ly speaking, he s uc u e wi h PDB iden i y numbe 1ny9 ha ing chain iden i ie A and is he 8 h s uc u e in he NMR ensemble. This was chosen on he g ounds ha i was he closes o he a e age s uc u e in ha ensemble and he e o e deemed o be mos ep esen a i e. The sequence o each o hese p o eins was hen submi ed o he P edic P o ein se e [18]. P edic ed s uc u al pa ame e s we e ex ac ed om he ou pu iles om his se e ( his was done manually bu an au oma ed e sion is unde de elopmen ). The s uc u al pa ame e s included in ou schemes we e: ●SeqNo - Sequence numbe o a he posi ion unde conside a ion ●AA - iden i y o he amino acid esidue a he posi ion ●OHEL - Obse ed seconda y s uc u e ●PHEL - P edic ed seconda y s uc u e ●OACC - Obse ed sol en accessibili y ●PACC - P edic ed sol en accessibili y The abo e a e all ob ained di ec ly as ou pu s om P edic P o ein. OHEL and PHEL employ he HST e minology [19] whe eby H s ands o α-helix, S o β-s and and T o u n. In p ac ice we employed he augmen ed se de ined wi hin he WHAT IF p og am whe eby H, S, and T a e de ined as be o e [19] and impo an seconda y s uc u e ea u es no included in HST a e added: 3 o 3 10 - helix and C o coil. The impo ance o dis inguishing C om T is ha he o me has he cha ac e o “ andom coil”while u ns con o m o s ingen limi s on backbone o sion angles. N.B. in much o he bioin o ma ics li e a u e E (“ex ended”) is used ins ead o S. Fo his wo k, a py hon sc ip was w i en o A icle No~e00175 4h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). ex ac hese da a bu he e is e e y likelihood ha his will be ully au oma ed in he nea u u e. While he P edic P o ein p og am always e u ns a PHEL and PACC alue, i does no always gi e he co esponding OHEL and OACC alues. In such cases, he co esponding obse ed alues can be de e mined using WHAT IF, o o he p o ein modelling so wa e. In ou case, we we e only in e es ed in OHEL and OACC in aining examples. When a p o ein wi h unknown c ys al s uc u e is s udied he da a will by de ini ion no be a ailable. I is o his eason ha PHEL and PACC a e men ioned, since he e may be many easons why esea che s migh wan o s udy p o eins ha lack a c ys al s uc u e (mu an s o example). Finally, we included s uc u e in o ma ion no gene a ed by P edic P o ein: AAH −Amino-acid hyd opa hy − alues o each o he 20 amino acid esidue ypes a e ob ained om a da abase [20] ha p o ides he cu en ly mos eliable se o da a. The hyd opa hy da a a e an impo an ea u e o he o e all co pus o p o ein s uc u al in o ma ion, bu he e is a p oblem in ha alues o ce ain pai s o amino acid ypes, o example Asp and Glu, and A g and Lys, a e e y close o one ano he , which a he masks he dis inc ly di e en s uc u al p opensi ies ha hese esidue ypes ha e (see Table 1). 2.2. Soni ica ion o p o ein sequence and p ope y da a The inpu da a o he h ee p o eins selec ed o his s udy a e lis ed in supplemen a y ables 1–3. The columns con ain bo h expe imen ally de i ed da a and da a de i ed om p edic ion me hods. The da a we e con e ed in o a o ma ha can be assimila ed by he musicalgo i hms Web-based so wa e [21]. 2.3. Da a soni ica ion mapping In o de o disce n da a pa e ns mos clea ly as melodic exp essions, he da a- o- music mappings ocused p ima ily on pi ch wi h uni o m hy hmic du a ions, and pi ch wi h some hy hmic a ie y. Fu u e in es iga ions wi h musical e inemen s should include seconda y cha ac e is ics such as imb e, dynamics, and a icula- ions. The da a- o-music mapping o amino acid chains was based on a p opo iona e expansion algo i hm ha ans o ms amino acid alues o i a musical ange. The amino acid alues om supplemen a y able 1 we e d awn om co esponding whole- esidue hyd ophobici y measu emen s (a e a e aging) wi hin he wa e o oc anol ange ob ained om he blanco.biomol.uci.edu Web si e, and lis ed in Table 1. The mapping esul s can be displayed as a musical scale ascending om A icle No~e00175 5h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). a oma ic o cha ged ypes wi h 17 disc e e pi ches assigned o he ange o 20 amino acids (see Fig. 1 and supplemen a y Audio 1). No e, in h ee cases amino acids we e pai ed up o sha e a single pi ch: M and Y, G and H, and A and S. The e is no pa icula a p io i a ionale o hese pai ings, bu he e a e some possible Table 1. AA hyd opa hy scale wi h a e aging; adap ed om o iginal da a [20] and modi ied o enhanced disc imina ion. AA AA-Hyd opa hy A e ages W -2.1 F -1.7 L -1.3 I -1.1 Y -0.7 M -0.7 V -0.5 C 0.0 P 0.1 T 0.3 S 0.5 A 0.5 Q 0.8 N 0.9 G 1.2 H 1.2 R 1.8 E 1.9 D 2.0 K 2.8 [(Fig._1)TD$FIG] Fig. 1. Musical scale c ea ed om AA whole- esidue hyd ophobici y measu emen s (a e a e aging). A icle No~e00175 6h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). biophysical explana ions o he M/Y and A/S pai s. The la e esidue ypes bo h ep esen he “small side-chain”class o esidues and hey can indeed “ eplace” each o he −examples o en ies in mul iple sequence alignmen s ha ead some hing like “AAAAASSSASAAAAASSAAAA”a e e y common. The M/Y case is a bi mo e sub le. M is simila o Y bu also o F and W. They a e all membe s o he “bulky side-chain”g oup and M can in many ins ances eplace he o he h ee. The case o G and H, hese also need some explaining since H is hough o in e ms o i s highly pola and ∼50% (a physiological pH) cha ged side chain while G has no side chain. On he scale used he e, hese wo lie e y close oge he , bu ha is also he case wi h se e al o he hyd opa hy scales. Mos o he expe imen al echniques used o de e mine hese scales ely in one way o ano he on pa i ioning be ween wo phases. We ha e o accep he ac ha H dis ibu es i sel ac oss hese wo phases in much he same way as does G. In he aqueous phase he ela i e popula ion o he cha ged species would be de e mined by he pH, while in he nonpola phase only he uncha ged species would be p esen . A p opo iona e expansion algo i hm was used o dis ibu e p o ein alues wi hin a designa ed pi ch ange as de ined by he use . The e is lexibili y in se ing he des ina ion pi ch span o wide o na ow anges, so ha use s can shape he musical esul s acco ding o lis ene p e e ences. In any se ing, he esul s will demons a e some p edic abili y, o example, T p (W), wi h an a e age hyd opa hy alue o −2.09, will always ancho he lowes end o he chosen pi ch ange; Lys (K), wi h an a e age hyd opa hy alue o 2.80, will always map o he highes end o he pi ch ange; and Se (S), wi h an a e age hyd opa hy alue o 0.46 will map o he middle o he pi ch ange. In his s udy, he AA alues we e mapped o a pi ch span o 55 musical no es: piano keys 25–80 (see Fig. 2 and supplemen a y Audio 2). This se ing p o ided a ela i ely e en dis ibu ion o independen pi ches o 17 AA alues. The same mapping dis ibu ion can apply o a ange o musical du a ions. In hese cases a se o musical du a ions om sho o long can be associa ed wi h nume ical da a alues om low o high; howe e , no hy hmic a ie y was added a his ime so ha he complexi ies o he 17-pi ch scale could be p esen ed in a simpli ied o m. Hence, each pi ch in he melodic ou pu was ep esen ed by a uni o m hy hmic alue. [(Fig._2)TD$FIG] Fig. 2. In oduc o y exce p om 1ny9 sco e ep esen ing AA hyd ophobici y alues. A icle No~e00175 7h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). The da a- o-music mapping o OHEL alues o e ed he challenge o con e ing shapes in o music. This app oach equi ed a p elimina y s ep ha ans o med OHEL da a in o “shaped”nume ic sequences, which we e hen soni ied o sho musical ges u es −called mo i es and sub-ph ases: Coil (C) = 1.0, 0.5, 0.8, 0.5, 1.0, 1.5, 1.2 Tu n (T) = 2.3, 1.7, 1.7, 2.0, 2.3 3 10 -helix (3) = 3.0, 2.8, 3.0, 3.2 α-helix (H) = 2.0, 1.6, 1.8, 2.2, 2.4 β-s and (S) o Ex ended (E) = 6.0, 5.8 The nume ic ep esen a ion o each shape can be lexibly mapped wi h he p opo iona e expansion algo i hm o a a ie y o musical anges ha will expand o comp ess he shapes on a e ical pi ch space (o axis). In music we call his augmen ing o diminishing he in e als, which a e he dis ances be ween pi ches. The choice o musical ange, whe he by expansion o comp ession, can also al e he gene al onali y o he esul s and he size o he hy hmic du a ions. Hence he choice o musical ange should be ca e ully conside ed o mee he goals o he analysis and lis ene p e e ences o encou age epea ed lis ening. The OHEL p o ein da a o 1 75 consis o a sequence o shapes labeled C, H, T, S. Each p o ein esidue shape is mi o ed by a musical mo i e o simila con ou . In his case he soni ica ion o one da a poin (o shape) will ea u e a sho collec ion o pi ches a he han a single pi ch as seen in he p e ious mapping o AA hyd opa hy. Fo example, he T (o u n) migh be ep esen ed by he nea ly conjunc musical mo i e: Ab-F-F-F#-Ab. This descending and ascending musical ges u e has a U shape, which mi o s he geome y o he T s uc u e (dihed al angles a anged so ha he chain e e ses). As ano he example, 3 10 , a epea ing egula s uc u e, is ep esen ed musically by epea ing pi ches as i in oscilla ion, such as: B-Bb-B-C. In his s udy each OHEL shape om 1 75 is ep esen ed by a mo i ic pa e n o pi ches and wi h a ied hy hms ha adhe e o he same p opo iona e mapping sys em (see Fig. 3 and supplemen a y Audio 3), whe e la ge alues such as 6.0 gene a e long hy hmic du a ions and small alues such as 0.5 become sho hy hmic du a ions. The OACC alues co espond o su ace and dep h ela ions o he in e io o he p o ein s uc u e. The OACC da a poin s a e mapped o he ull ange o he piano o cap u e he a ying su ace- o-dep h ela ionships. In his melodic soni ica ion, pi ch is he only poin o ocus as an e ec i e musical cha ac e is ic o ack da a su ace o dep h ela ions. In his example, dep h is ep esen ed by he deep sounding low pi ch con en , and su ace a eas by high pi ch con en . The uni o m hy hmic du a ions a a s eady empo, o pulse, help he lis ene ocus on essen ial A icle No~e00175 8h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). cha ac e is ics o ascending and descending pi ches (see Fig. 4 and supplemen a y Audio 4). The OACC alues we e mapped by means o he na u al log algo i hm. The log algo i hm was selec ed o add pi ch space o he low and mid ange alues, gi ing hem mo e sepa a ion o cla i y and de ini ion han he al e na i e p opo iona e mapping sys em wi h equal dis ibu ion. The log mapping sys em is ideal as i s e ches he a ailable low pi ch space and na ows he a ailable span o high pi ch space o accommoda e a la ge po ion o low ange da a poin s o he p o ein [(Fig._3)TD$FIG] Fig. 3. In oduc o y exce p om 1 75 sco e ep esen ing OHEL alues. [(Fig._4)TD$FIG] Fig. 4. In oduc o y exce p om 4ake sco e ep esen ing OACC alues. A icle No~e00175 9h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). Table 2. Pe cep ual soni ica ion su ey esul s. OHEL and con ols used eal ime isual cues, while AA and OACC soni ica ion exce p s used no eal ime isual cues. Pa icipan s we e able o pe cei e simila i ies be ween isual ep esen a ions and audible melodies gene a ed by he same da a. Pa icipan s Soni ica ion Pe cep ual Su ey (Human Subjec s 1-38) Con ol An icipa ing Posi i e ("A" o "D" Responses) Con ol An icipa ing Nega i e ("B" o "C" Responses) AA 1ny9 exce p OACC 4ake exce p OHEL 1 75 comple e AA 1ny9 in de ail Subjec #1 C B A A D N/A Subjec #2 A B A A A N/A Subjec #3 A B C B D C Subjec #4 A B C C A C Subjec #5 D C D A A A Subjec #6 D B A D D D Subjec #7 D B D D D A Subjec #8 D A C A D D Subjec #9 A B D A D D Subjec #10 A D A A C C Subjec #11 D B A A D A Subjec #12 A B A D A D Subjec #13 A B D D A A Subjec #14 A C A D A A Subjec #15 A C A A D A Subjec #16 A C D D A A Subjec #17 D A B D D D Subjec #18 A C A D D C Subjec #19 D B B C A D Subjec #20 A B A B A D Subjec #21 A B A A A A Subjec #22 D B B B C C Subjec #23 D B A D D A (Con inued) A icle No~e00175 16 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). Table 2.(Con inued) Pa icipan s Soni ica ion Pe cep ual Su ey (Human Subjec s 1-38) Con ol An icipa ing Posi i e ("A" o "D" Responses) Con ol An icipa ing Nega i e ("B" o "C" Responses) AA 1ny9 exce p OACC 4ake exce p OHEL 1 75 comple e AA 1ny9 in de ail Subjec #24 A B C C C A Subjec #25 A B C C D A Subjec #26 A B A A D A Subjec #27 A B A A A A Subjec #28 D B A A A A Subjec #29 C B A A A A Subjec #30 A C A A D A Subjec #31 A C A D C D Subjec #32 A B D C A C Subjec #33 A B A A A A Subjec #34 A C A A A A Subjec #35 D C A A D A Subjec #36 D B A C C D Subjec #37 C B B B D B Subjec #38 A B A A D A To al Pe cen ages o Response Types A Simila 60.53% 5.26% 60.53% 47.37% 42.11% 55.56% B No Simila 0.00% 68.42% 10.53% 10.53% 0.00% 2.78% C Somewha Simila 7.89% 23.68% 13.16% 15.79% 13.16% 16.67% D Mos ly Simila 31.58% 2.63% 15.79% 26.32% 44.74% 25.00% A icle No~e00175 17 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). 4. Discussion We ha e sugges ed se e al ways in which p o ein sequences can be “hea d” a he han “ ead”. The amino acid sequence is ende ed as a s ing o musical no es wi h sound quali ies ha e lec he p ope ies o hese esidues. The e a e se e al di e en ways o encoding hese p ope ies and we ha e examined se e al o hese, all wi h in e es ing and memo able, bu di e en ou comes. Ce ain o hese (OACC/PACC and AA) possess he p ope y o ha ing a 1:1 a io be ween pi ches and esidues, while OHEL/PHEL has been cons uc ed speci ically in o de o cap u e he de ining s uc u al ea u e o each seconda y s uc u e ype (e.g. 2 pi ches o S/E, 3 pi ches o 3 10 , and 4 pi ches o α-helix). By lis ening o a melodic shape o a gi en p o ein sequence, an imp ession o i s s uc u e can be buil up. We p opose his as an excellen lea ning ool o hose wishing be e o unde s and and disc imina e p o ein old s uc u es, and as an aid o old iden i ica ion i sel . We in end o ex end his wo k owa ds a mo e comple e domain old iden i ica ion sys em, so ha wi h p ac ice, and by compa ison wi h he sounds co esponding o o he p o ein ypes, his can lead o a way o ecognizing he 3D olds o di e en p o eins. Fu he , we a e awa e ha p o eins a e lexible en i ies ha ypically swi ch be ween wo di e en s uc u es in he cou se o exe cising hei unc ion [22]. I would be in e es ing i ou musical app oach could help o iden i y he signa u es co esponding o he esidue posi ions ha a e esponsible o his pa icula ly impo an p o ein unc ion. The musical pa e ns a e complex, and his will no only be because p o ein olds a e complex bu also due o he need o swi ch be ween di e en s uc u al s a es. The p ima y sequence o p o eins has o ca e o mo e han olding and swi ching be ween olds, bu o a whole ange o o he unc ions [22] including how he p o ein a i es a i s des ina ion in (o ou side) he cell, which equi es he a achmen o pos - ansla ional signals on i s su ace. These unc ions a e also encoded gene ically [22]. Fo hese easons we expec he e o be many de elopmen s in he a ea whe e p o eomics and soni ica ion o e lap. We should men ion ha simila a en ion is being paid o soni ica ion o DNA sequences and gene exp ession [23,24]. These also encapsula e s uc u al in o ma ion bu in a somewha di e en way, he p o ein sequences a e mo e closely ela ed o he e en s ha ac ually ake place a he pheno ypic le el in he li ing cell. These p o ein sequences a e encoded in DNA bu he la e can also encompass egions ha ha e o do wi h cell di e en ia ion and epigene ic con ol [24] which a e ou side o and dis inc om he p o ein coding egions. Thus he e is e e y eason o engage in soni ica ion s udies a he DNA le el also. A icle No~e00175 18 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). Decla a ions Au ho con ibu ion s a emen Robe P. Bywa e , Jona han N. Middle on: Concei ed and designed he expe imen s; Pe o med he expe imen s; Analyzed and in e p e ed he da a; Con ibu ed eagen s, ma e ials, analysis ools o da a; W o e he pape . Funding s a emen This wo k was suppo ed by an Eas e n Washing on Uni e si y Facul y Resea ch and C ea i e Wo ks Summe G an . This wo k was also suppo ed in pa by Tekes −The Finnish unding agency o inno a ion (decision 40296/14). Compe ing in e es s a emen The au ho s decla e no con lic o in e es . Addi ional in o ma ion Supplemen a y con en ela ed o his a icle has been published online a 10.1016/ j.heliyon.2016.e00175. Acknowledgemen s The au ho s would like o acknowledge he suppo o Eas e n Washing on Uni e si y and he Uni e si y o Tampe e o helping us mo e soni ica ion esea ch o wa d in he con ex o biological sciences. Re e ences [1] G. Bellesia, A.I. Jewe , J.E. Shea, Sequence pe iodici y and seconda y s uc u e p opensi y in model p o eins, P o ein Sci. 19 (2010) 141–154. [2] S. Ho mölle , T.P. Zhou, T. Ohlson, Con o ma ions o amino acids in p o eins, Ac a C ys . D 58 (2002) 768–776. [3] R.P. Bywa e , D. Thomas, G. V iend, A sequence and s uc u al s udy o ansmemb ane helices, J. Compu -Aided Mol. Des. 15 (2001) 533–552. [4] R.P. Bywa e , V. Ve yazo , The p e e ed con o ma ion o dipep ides in he con ex o biosyn hesis, Na u wissenscha en 100 (2013) 853–859. [5] A.G.Mu zin,S.E.B enne ,T.Hubba d,e al.,SCOP:as uc u al classi ica ion o p o eins da abase o he in es iga ion o sequences and s uc u es, J. Mol. Biol. 247 (1995) 536–540. A icle No~e00175 19 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). [6] C.A. O engo, A.D. Michie, S. Jones, e al., CATH −a hie a chic classi ica ion o p o ein domain s uc u es, S uc u e 15 (1997) 1093–1108. [7] N. Koga, R. Ta sumi-Koga, G.H. Liu, T.B. Ac on, G.T. Mon elione, D. Bake , e al., P inciples o designing ideal p o ein s uc u es, Na u e 491 (2012) 222–227. [8] S. Ba ass, P. Vicke s, Soni ica ion design and aes he ics, The Soni ica ion Handbook, Logos Ve lag, 2011, pp. 145–172. [9] B.N. Walke , G. K ame , Mappings and me apho s in audi o y displays: an expe imen assessmen , ACM T ans. Appl. Pe cep . 2 (4) (2005) 407–412. [10] The Soni ica ion Handbook, In: T. He mann, A. Hun , J.G. Neuho (Eds.), Logos Ve lag, 2011. [11] F. Dombois, G. Eckel, Audi ica ion, The Soni ica ion Handbook, Logos Ve lag, 2011. [12] J. Dunn, M.A. Cla k, Li e music: The soni ica ion o p o eins, Leona do 32 (1) (1999) 25–32. [13] R. Takahashi, J.H. Mille , Con e sion o amino-acid sequences in p o eins o classical music: Sea ch o audi o y pa e ns, Genome Biol. 8 (2007) 405. [14] M.A. Ga cia-Ruiz, J.R. Gui e ez-Pulido, An o e iew o audi o y display o assis comp ehension o molecula in o ma ion, In e ac . Compu . 18 (2006) 853–868. [15] A. Suppe , Sublime equencies: he cons uc ion o sublime lis ening expe iences in he soni ica ion o scien i ic da a, Soc. S ud. Sci. 44 (1) (2014) 34–58. [16] P. Mina y, M. Le i , P obing p o ein old space wi h a simpli ied model, J. Mol. Biol. 375 (2008) 920–933. [17] G. V iend, WHAT IF: a molecula modelling and d ug design p og am, J. Mol. G aph. 8 (1990) 52–56. [18] B. Ros , G. Yachda , J.F. Liu, The P edic P o ein se e , Nucl. Acids Res. 32 (2004) W321–W326. [19] W. Kabsch, C. Sande , Dic iona y o p o ein seconda y s uc u e: pa e n ecogni ion o hyd ogen-bonded and geome ical ea u es, Biopolyme s 22 (1983) 2577–2637. [20] W.C. Wimley, S.H. Whi e, Memb ane pa i ioning: Dis inguishing bilaye e ec s om he hyd ophobic e ec , Biochemis y 32 (1993) 6307–6312. A icle No~e00175 20 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/). [21] J. Middle on, D. Dowd, Web-based algo i hmic composi ion om ex amu- sical esou ces, Leona do 41 (2) (2008) 128–135. [22] R.P. Bywa e , P o ein olding: a p oblem wi h mul iple solu ions, J. Biomol. S uc . Dyn. 31 (4) (2013) 351–362. [23] M.S. S aege, A sho ea ise conce ning a musical app oach o he in e p e a ion o gene exp ession da a, Sci. Rep. 5 (2015) 15281. [24] D. B ocks, Musical pa e ns o compa a i e epigenomics, Clin. Epigene ics 7 (2015) 94. A icle No~e00175 21 h p://dx.doi.o g/10.1016/j.heliyon.2016.e00175 2405-8440/© 2016 The Au ho s. Published by Else ie L d. This is an open access a icle unde he CC BY-NC-ND license (h p://c ea i ecommons.o g/licenses/by-nc-nd/4.0/).