Nasarre, C., Roth, M., Jacob, L., Roth, L., Koncina, E., Thien, A., Labourdette, G., Poulet, P., Hubert, P., Crémel, G.,
Roussel, G., Aunis, D., Bagnard, D. (2010) Peptide-based interference of the transmembrane domain of neuropilin-1
inhibits glioma growth in vivo. Oncogene 29:2381–2392.
Nikaido, H. (1992) Porins and specific channels of bacterial outer membranes. Molec. Microbiol. 6:435–442.
Pal, S., Barnhart, K.M., Wei, Q., Abai, A.M., Peterson, E.M., de la Maza, L.M. (1999) Vaccination of mice with DNA
plasmids coding for the Chlamydia trachomatis major outer membrane protein elicits an immune response but fails to
protect against a genital challenge. Vaccine 17:459–465.
Pal, S., Davis, H.L., Peterson, E.M., de la Maza, L.M. (2002) Immunization with the Chlamydia trachomatis mouse
pneumonitis major outer membrane protein by use of CpG oligodeoxynucleotides as an adjuvant induces a protective
immune response against an intranasal chlamydial challenge. Infect. Immun. 70:4812–4817.
Pal, S., Peterson, E.M., de la Maza, L.M. (2005) Vaccination with the Chlamydia trachomatis major outer membrane
protein can elicit an immune response as protective as that resulting from inoculation with live bacteria. Infect.
Immun. 73:8153–8160.
Plotkin, S.A., Orenstein, W.A., Offit, P.A., Edwards, K.M. (2017) Vaccines, 7th ed., Elsevier, New York, N.Y., 1720 p.
Polovinkin, V., Gushchin, I., Balandin, T., Chervakov, P., Round, E., Shevchenko, V., Popov, A., Borshchevskiy, V.,
Popot, J.-L., Gordeliy, V. (2014) High-resolution structure of a membrane protein transferred from amphipol to a
lipidic mesophase. J. Membr. Biol. 247:997–1004.
Popot, J.-L. (2014) Folding membrane proteins in vitro: A table and some comments. Arch. Biochem. Biophys.
564:314–326.
Popot, J.-L., Berry, E.A., Charvolin, D., Creuzenet, C., Ebel, C., Engelman, D.M., Flötenmeyer, M., Giusti, F., Gohon,
Y., Hervé, P., Hong, Q., Lakey, J.H., Leonard, K., Shuman, H.A., Timmins, P., Warschawski, D.E., Zito, F.,
Zoonens, M., Pucci, B., Tribet, C. (2003) Amphipols: polymeric surfactants for membrane biology research. Cell.
Mol. Life Sci. 60:1559–1574.
Popot, J.-L., Althoff, T., Bagnard, D., Banères, J.-L., Bazzacco, P., Billon-Denis, E., Catoire, L.J., Champeil, P.,
Charvolin, D., Cocco, M.J., Crémel, G., Dahmane, T., de la Maza, L.M., Ebel, C., Gabel, F., Giusti, F., Gohon,
Y., Goormaghtigh, E., Guittet, E., Kleinschmidt, J.H., Kühlbrandt, W., Le Bon, C., Martinez, K.L., Picard, M., Pucci,
B., Rappaport, F., Sachs, J.N., Tribet, C., van Heijenoort, C., Wien, F., Zito, F., Zoonens, M. (2011) Amphipols from
A to Z. Annu. Rev. Biophys. 40:379–408.
Pulendran, B., Ahmed, R. (2011) Immunological mechanisms of vaccination. Nat. Immunol. 12:509–517.
Reddy, S.T., van der Vlies, A.J., Simeoni, E., Angeli, V., Randolph, G.J., O’Neil, C.P., Lee, L.K., Swartz, M.A.,
Hubbell, J.A. (2007) Exploiting lymphatic transport and complement activation in nanoparticle vaccines. Nat.
Biotechnol. 25:1159–1164.
Rockey, D.D., Wang, J., Lei, L., Zhong, G. (2009) Chlamydia vaccine candidates and tools for chlamydial antigen
discovery. Expert Rev. Vaccines 8:1365–1377.
Rodriguez-Maranon, M.J., Bush, R.M., Peterson, E.M., Schirmer, T., de la Maza, L.M. (2002) Prediction of the
membrane-spanning β-strands of the major outer membrane protein of Chlamydia. Protein Sci. 11:1854–1861.
Roth, L., Nasarre, C., Dirrig-Grosch, S., Aunis, D., Crémel, G., Hubert, P., Bagnard, D. (2008) Transmembrane domain
interactions control biological functions of neuropilin-1. Mol. Biol. Cell 19:646–654.
Roth, L., Koncina, E., Satkauskas, S., Crémel, G., Aunis, D., Bagnard, D. (2009) The many faces of semaphorins: From
development to pathology. Cell. Mol. Life Sci. 66:649–666.
Sachan, S., Ramakrishnan, S., Annamalai, A., Sharma, B.K., Malik, H., Saravanan, B.C., Jain, L., Saxena, M., Kumar,
A., Krishnaswamy, N. (2015) Adjuvant potential of resiquimod with inactivated Newcastle disease vaccine and its
mechanism of action in chicken. Vaccine 33:4526–4532.
Sanderson, S.D., Thoman, M.L., Kis, K., Virts, E.L., Herrera, E.B., Widmann, S., Sepulveda, H., Phillips, J.A. (2012)
Innate immune induction and influenza protection elicited by a response-selective agonist of human C5a. PLoS One
7:e40303.
Sato, Y., Hatakeyama, H., Sakurai, Y., Hyodo, M., Akita, H., Harashima, H. (2012) A pH-sensitive cationic lipid
facilitates the delivery of liposomal siRNA and gene silencing activity in vitro and in vivo. J. Control. Release
163:267–276.
Schachter, J. (1999) Infection and disease epidemiology, in: Stephens, R.S., ed., Chlamydia: Intracellular Biology,
Pathogenesis and Immunity, ASM, Washington, pp. 139–170.
Schachter, J., Dawson, C.R. (1978) Human Chlamydial Infections. PSG Pub. Co., Littleton, Mass., 273 p.
Seong, S.Y., Matzinger, P. (2004) Hydrophobicity: an ancient damage-associated molecular pattern that initiates innate
immune responses. Nat. Rev. Immunol. 4:469–478.
Serra-Batiste, M., Tolchard, J., Giusti, F., Zoonens, M., Carrula, N. (2018) Stabilization of a membrane-associated
amyloid-β oligomer for its validation in Alzheimer's disease. Front. Mol. Biosci. 5:38.
Sharma, K.S., Durand, G., Gabel, F., Bazzacco, P., Le Bon, C., Billon-Denis, E., Catoire, L.J., Popot, J.-L., Ebel, C.,
Pucci, B. (2012) Non-ionic amphiphilic homopolymers: Synthesis, solution properties, and biochemical validation.
Langmuir 28:4625–4639.
References
681
Roussel, G., Aunis, D., Bagnard, D. (2010) Peptide-based interference of the transmembrane domain of neuropilin-1
inhibits glioma growth in vivo. Oncogene 29:2381–2392.
Nikaido, H. (1992) Porins and specific channels of bacterial outer membranes. Molec. Microbiol. 6:435–442.
Pal, S., Barnhart, K.M., Wei, Q., Abai, A.M., Peterson, E.M., de la Maza, L.M. (1999) Vaccination of mice with DNA
plasmids coding for the Chlamydia trachomatis major outer membrane protein elicits an immune response but fails to
protect against a genital challenge. Vaccine 17:459–465.
Pal, S., Davis, H.L., Peterson, E.M., de la Maza, L.M. (2002) Immunization with the Chlamydia trachomatis mouse
pneumonitis major outer membrane protein by use of CpG oligodeoxynucleotides as an adjuvant induces a protective
immune response against an intranasal chlamydial challenge. Infect. Immun. 70:4812–4817.
Pal, S., Peterson, E.M., de la Maza, L.M. (2005) Vaccination with the Chlamydia trachomatis major outer membrane
protein can elicit an immune response as protective as that resulting from inoculation with live bacteria. Infect.
Immun. 73:8153–8160.
Plotkin, S.A., Orenstein, W.A., Offit, P.A., Edwards, K.M. (2017) Vaccines, 7th ed., Elsevier, New York, N.Y., 1720 p.
Polovinkin, V., Gushchin, I., Balandin, T., Chervakov, P., Round, E., Shevchenko, V., Popov, A., Borshchevskiy, V.,
Popot, J.-L., Gordeliy, V. (2014) High-resolution structure of a membrane protein transferred from amphipol to a
lipidic mesophase. J. Membr. Biol. 247:997–1004.
Popot, J.-L. (2014) Folding membrane proteins in vitro: A table and some comments. Arch. Biochem. Biophys.
564:314–326.
Popot, J.-L., Berry, E.A., Charvolin, D., Creuzenet, C., Ebel, C., Engelman, D.M., Flötenmeyer, M., Giusti, F., Gohon,
Y., Hervé, P., Hong, Q., Lakey, J.H., Leonard, K., Shuman, H.A., Timmins, P., Warschawski, D.E., Zito, F.,
Zoonens, M., Pucci, B., Tribet, C. (2003) Amphipols: polymeric surfactants for membrane biology research. Cell.
Mol. Life Sci. 60:1559–1574.
Popot, J.-L., Althoff, T., Bagnard, D., Banères, J.-L., Bazzacco, P., Billon-Denis, E., Catoire, L.J., Champeil, P.,
Charvolin, D., Cocco, M.J., Crémel, G., Dahmane, T., de la Maza, L.M., Ebel, C., Gabel, F., Giusti, F., Gohon,
Y., Goormaghtigh, E., Guittet, E., Kleinschmidt, J.H., Kühlbrandt, W., Le Bon, C., Martinez, K.L., Picard, M., Pucci,
B., Rappaport, F., Sachs, J.N., Tribet, C., van Heijenoort, C., Wien, F., Zito, F., Zoonens, M. (2011) Amphipols from
A to Z. Annu. Rev. Biophys. 40:379–408.
Pulendran, B., Ahmed, R. (2011) Immunological mechanisms of vaccination. Nat. Immunol. 12:509–517.
Reddy, S.T., van der Vlies, A.J., Simeoni, E., Angeli, V., Randolph, G.J., O’Neil, C.P., Lee, L.K., Swartz, M.A.,
Hubbell, J.A. (2007) Exploiting lymphatic transport and complement activation in nanoparticle vaccines. Nat.
Biotechnol. 25:1159–1164.
Rockey, D.D., Wang, J., Lei, L., Zhong, G. (2009) Chlamydia vaccine candidates and tools for chlamydial antigen
discovery. Expert Rev. Vaccines 8:1365–1377.
Rodriguez-Maranon, M.J., Bush, R.M., Peterson, E.M., Schirmer, T., de la Maza, L.M. (2002) Prediction of the
membrane-spanning β-strands of the major outer membrane protein of Chlamydia. Protein Sci. 11:1854–1861.
Roth, L., Nasarre, C., Dirrig-Grosch, S., Aunis, D., Crémel, G., Hubert, P., Bagnard, D. (2008) Transmembrane domain
interactions control biological functions of neuropilin-1. Mol. Biol. Cell 19:646–654.
Roth, L., Koncina, E., Satkauskas, S., Crémel, G., Aunis, D., Bagnard, D. (2009) The many faces of semaphorins: From
development to pathology. Cell. Mol. Life Sci. 66:649–666.
Sachan, S., Ramakrishnan, S., Annamalai, A., Sharma, B.K., Malik, H., Saravanan, B.C., Jain, L., Saxena, M., Kumar,
A., Krishnaswamy, N. (2015) Adjuvant potential of resiquimod with inactivated Newcastle disease vaccine and its
mechanism of action in chicken. Vaccine 33:4526–4532.
Sanderson, S.D., Thoman, M.L., Kis, K., Virts, E.L., Herrera, E.B., Widmann, S., Sepulveda, H., Phillips, J.A. (2012)
Innate immune induction and influenza protection elicited by a response-selective agonist of human C5a. PLoS One
7:e40303.
Sato, Y., Hatakeyama, H., Sakurai, Y., Hyodo, M., Akita, H., Harashima, H. (2012) A pH-sensitive cationic lipid
facilitates the delivery of liposomal siRNA and gene silencing activity in vitro and in vivo. J. Control. Release
163:267–276.
Schachter, J. (1999) Infection and disease epidemiology, in: Stephens, R.S., ed., Chlamydia: Intracellular Biology,
Pathogenesis and Immunity, ASM, Washington, pp. 139–170.
Schachter, J., Dawson, C.R. (1978) Human Chlamydial Infections. PSG Pub. Co., Littleton, Mass., 273 p.
Seong, S.Y., Matzinger, P. (2004) Hydrophobicity: an ancient damage-associated molecular pattern that initiates innate
immune responses. Nat. Rev. Immunol. 4:469–478.
Serra-Batiste, M., Tolchard, J., Giusti, F., Zoonens, M., Carrula, N. (2018) Stabilization of a membrane-associated
amyloid-β oligomer for its validation in Alzheimer's disease. Front. Mol. Biosci. 5:38.
Sharma, K.S., Durand, G., Gabel, F., Bazzacco, P., Le Bon, C., Billon-Denis, E., Catoire, L.J., Popot, J.-L., Ebel, C.,
Pucci, B. (2012) Non-ionic amphiphilic homopolymers: Synthesis, solution properties, and biochemical validation.
Langmuir 28:4625–4639.
References
681